{"id":1743,"date":"2024-02-01T10:41:00","date_gmt":"2024-02-01T01:41:00","guid":{"rendered":"http:\/\/www.matsuo-lab.net\/?page_id=1743"},"modified":"2024-02-22T19:51:57","modified_gmt":"2024-02-22T10:51:57","slug":"prof-matsuo-en","status":"publish","type":"page","link":"https:\/\/www.matsuo-lab.net\/?page_id=1743&lang=en","title":{"rendered":"prof.matsuo-en"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"1743\" class=\"elementor elementor-1743\" data-elementor-post-type=\"page\">\n\t\t\t\t<div class=\"elementor-element elementor-element-8e9b028 e-flex e-con-boxed e-con e-parent\" data-id=\"8e9b028\" data-element_type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;,&quot;content_width&quot;:&quot;boxed&quot;}\" data-core-v316-plus=\"true\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-ccce99e service_title elementor-widget elementor-widget-heading\" data-id=\"ccce99e\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.19.0 - 28-02-2024 *\/\n.elementor-heading-title{padding:0;margin:0;line-height:1}.elementor-widget-heading .elementor-heading-title[class*=elementor-size-]>a{color:inherit;font-size:inherit;line-height:inherit}.elementor-widget-heading .elementor-heading-title.elementor-size-small{font-size:15px}.elementor-widget-heading .elementor-heading-title.elementor-size-medium{font-size:19px}.elementor-widget-heading .elementor-heading-title.elementor-size-large{font-size:29px}.elementor-widget-heading .elementor-heading-title.elementor-size-xl{font-size:39px}.elementor-widget-heading .elementor-heading-title.elementor-size-xxl{font-size:59px}<\/style><h1 class=\"elementor-heading-title elementor-size-default\">Member<\/h1>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-d7466f7 e-flex e-con-boxed e-con e-parent\" data-id=\"d7466f7\" data-element_type=\"container\" data-settings=\"{&quot;content_width&quot;:&quot;boxed&quot;}\" data-core-v316-plus=\"true\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-234f23e e-flex e-con-boxed e-con e-child\" data-id=\"234f23e\" data-element_type=\"container\" data-settings=\"{&quot;content_width&quot;:&quot;boxed&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-594adc3 elementor-widget elementor-widget-shortcode\" data-id=\"594adc3\" data-element_type=\"widget\" data-widget_type=\"shortcode.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"elementor-shortcode\"><div class=\"breadcrumbs\"><span property=\"itemListElement\" typeof=\"ListItem\"><a property=\"item\" typeof=\"WebPage\" title=\"\u677e\u5c3e\u7814\u7a76\u5ba4 Matsuo Group \u540d\u53e4\u5c4b\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u79d1\u5316\u5b66\u30b7\u30b9\u30c6\u30e0\u5de5\u5b66\u5c02\u653b\u3078\u79fb\u52d5\u3059\u308b\" href=\"https:\/\/www.matsuo-lab.net\" class=\"home\" aria-current=\"page\"><span property=\"name\">TOP<\/span><\/a><meta property=\"position\" content=\"1\"><\/span><\/div><\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-7343cb4 member e-flex e-con-boxed e-con e-child\" data-id=\"7343cb4\" data-element_type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;,&quot;content_width&quot;:&quot;boxed&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-a825475 elementor-widget-divider--view-line elementor-widget elementor-widget-divider\" data-id=\"a825475\" data-element_type=\"widget\" data-widget_type=\"divider.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.19.0 - 28-02-2024 *\/\n.elementor-widget-divider{--divider-border-style:none;--divider-border-width:1px;--divider-color:#0c0d0e;--divider-icon-size:20px;--divider-element-spacing:10px;--divider-pattern-height:24px;--divider-pattern-size:20px;--divider-pattern-url:none;--divider-pattern-repeat:repeat-x}.elementor-widget-divider .elementor-divider{display:flex}.elementor-widget-divider .elementor-divider__text{font-size:15px;line-height:1;max-width:95%}.elementor-widget-divider .elementor-divider__element{margin:0 var(--divider-element-spacing);flex-shrink:0}.elementor-widget-divider .elementor-icon{font-size:var(--divider-icon-size)}.elementor-widget-divider .elementor-divider-separator{display:flex;margin:0;direction:ltr}.elementor-widget-divider--view-line_icon .elementor-divider-separator,.elementor-widget-divider--view-line_text 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100%;mask-size:var(--divider-pattern-size) 100%;-webkit-mask-repeat:var(--divider-pattern-repeat);mask-repeat:var(--divider-pattern-repeat);background-color:var(--divider-color);-webkit-mask-image:var(--divider-pattern-url);mask-image:var(--divider-pattern-url)}.elementor-widget-divider--no-spacing{--divider-pattern-size:auto}.elementor-widget-divider--bg-round{--divider-pattern-repeat:round}.rtl .elementor-widget-divider .elementor-divider__text{direction:rtl}.e-con-inner>.elementor-widget-divider,.e-con>.elementor-widget-divider{width:var(--container-widget-width,100%);--flex-grow:var(--container-widget-flex-grow)}<\/style>\t\t<div class=\"elementor-divider\">\n\t\t\t<span class=\"elementor-divider-separator\">\n\t\t\t\t\t\t<\/span>\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-1892e53 elementor-widget elementor-widget-heading\" data-id=\"1892e53\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">\u677e\u5c3e \u8c4a<\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-eca7bc9 elementor-widget elementor-widget-image\" data-id=\"eca7bc9\" data-element_type=\"widget\" data-widget_type=\"image.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.19.0 - 28-02-2024 *\/\n.elementor-widget-image{text-align:center}.elementor-widget-image a{display:inline-block}.elementor-widget-image a img[src$=\".svg\"]{width:48px}.elementor-widget-image img{vertical-align:middle;display:inline-block}<\/style>\t\t\t\t\t\t\t\t\t\t<img decoding=\"async\" width=\"112\" height=\"8\" src=\"https:\/\/www.matsuo-lab.net\/wp-content\/uploads\/2023\/09\/title_line.svg\" class=\"attachment-large size-large wp-image-265\" alt=\"\" \/>\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-d9016a4 elementor-widget elementor-widget-heading\" data-id=\"d9016a4\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Education<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-631fe8f elementor-widget elementor-widget-text-editor\" data-id=\"631fe8f\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<style>\/*! elementor - v3.19.0 - 28-02-2024 *\/\n.elementor-widget-text-editor.elementor-drop-cap-view-stacked .elementor-drop-cap{background-color:#69727d;color:#fff}.elementor-widget-text-editor.elementor-drop-cap-view-framed .elementor-drop-cap{color:#69727d;border:3px solid;background-color:transparent}.elementor-widget-text-editor:not(.elementor-drop-cap-view-default) .elementor-drop-cap{margin-top:8px}.elementor-widget-text-editor:not(.elementor-drop-cap-view-default) .elementor-drop-cap-letter{width:1em;height:1em}.elementor-widget-text-editor .elementor-drop-cap{float:left;text-align:center;line-height:1;font-size:50px}.elementor-widget-text-editor .elementor-drop-cap-letter{display:inline-block}<\/style>\t\t\t\t<p>1992\u20131996 Department of Chemistry, Faculty of Engineering Science, Osaka University<br \/>Awarded the degree of B.S. in chemistry<br \/>\u00a0<br \/>1996\u20132001 Department of Chemistry, Graduate School of Engineering Science, Osaka University<br \/>Awarded the degree of Ph.D. in chemistry under direction of Professors Kazuhide Tani and Kazushi Mashima<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-79735f2 elementor-widget elementor-widget-heading\" data-id=\"79735f2\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Research and Professional Experience<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2ee9b61 elementor-widget elementor-widget-text-editor\" data-id=\"2ee9b61\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p>1998\u20132001 \u3000Research Fellow of the Japan Society for the Promotion of Science (JSPS; DC1)<\/p>\n<p>2001\u20132004 \u3000Assistant Professor, Department of Chemistry, The University of Tokyo<\/p>\n<p>2004\u20132010 \u3000Group Leader, Functional Complex Group, Nakamura Functional Carbon Cluster Project, ERATO, Japan Science and Technology Agency<\/p>\n<p>2009-2016 \u3000 Project Professor, Department of Chemistry, The University of Tokyo<\/p>\n<p>2010\u00a0 \u00a0 \u00a0 \u00a0 \u3000\u3000 Visiting Professor, University of Strasbourg, France<\/p>\n<p>2013-\u00a0 \u00a0 \u00a0 \u00a0 \u3000\u00a0 \u00a0 Visiting Professor, University of Tsukuba<\/p>\n<p>2013-2014\u3000\u00a0 Visiting Professorships for Senior International Scientists, Institute of Chemistry, Chinese Academy of Sciences, China<\/p>\n<p>2016-2021 \u3000 Professor, Hefei National Laboratory for Physical Sciences at Microscale, and Department of Chemistry, School of Chemistry and Materials Science, University of Science and Technology of China<\/p>\n<p>2016-\u00a0 \u00a0 \u00a0 \u00a0 \u3000\u3000Project Professor, Department of Mechanical Engineering, School of Engineering, The University of Tokyo<\/p>\n<p>2016-2018 \u3000 Visiting Researcher, National Institute of Advanced Industrial Science and Technology (AIST)<\/p>\n<p>2016-2017\u3000\u00a0 Visiting Professor, Institute for Chemical Research, Kyoto University<\/p>\n<p>2018-\u00a0 \u00a0 \u00a0 \u00a0 \u3000\u00a0 \u00a0 Visiting Professor, New Industry Creation Hatchery Center, Tohoku University<\/p>\n<p>2019-\u00a0 \u00a0 \u00a0 \u00a0 \u3000\u00a0 \u00a0 Professor, Institute of Materials Innovation, Institutes of Innovation for Future Society, Nagoya University<\/p>\n<p>2020-\u00a0 \u00a0 \u00a0 \u00a0 \u3000\u00a0 \u00a0 Professor, Department of Chemical System Engineering, Graduate School of Engineering, Nagoya University<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-92338dc elementor-widget elementor-widget-heading\" data-id=\"92338dc\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Awards<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-33f2200 elementor-widget elementor-widget-text-editor\" data-id=\"33f2200\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p>2005\u3000\u3000The Chemical Society of Japan Award for Young Chemists<br \/>2007.2 \u3000The Osawa Award of the Fullerenes and Nanotubes Research Society<br \/>2007.7 \u3000Lectureship of Pedersen Seminar Series, DuPont<br \/>2007.9 \u3000The Young Scientists Award of the Japan Society of Coordination Chemistry<br \/>2010.2 \u3000Chemistry Innovation UT GCOE Lectureship Award<br \/>2010.4 \u3000The Young Scientists&#8217; Prize, The Commendation for Science and Technology by the Minister of Education, Culture, Sports, Science and Technology<br \/>2012.9 \u3000Nozoe Memorial Award for Young Organic Chemists<br \/>2012.11\u00a0 \u00a0Banyu Chemist Award<br \/>2014.1\u00a0 \u00a0 \u00a0 Thieme Chemistry Journal Award 2014<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-344ff21 elementor-widget elementor-widget-heading\" data-id=\"344ff21\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Research Fields<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5f4b6fd elementor-widget elementor-widget-text-editor\" data-id=\"5f4b6fd\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<div>\n<div>\n<p>Organic Solar Cells, Carbon Cluster Science, Organic Materials Chemistry, Organometallic Chemistry<\/p>\n<\/div>\n<\/div>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-3a62a28 elementor-widget elementor-widget-heading\" data-id=\"3a62a28\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Academic activities, social contribution<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-7b96131 elementor-widget elementor-widget-text-editor\" data-id=\"7b96131\" data-element_type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t<p>April 2010 &#8211; March 2012 Secretary, Chemical Society of Japan, Kanto Branch<\/p>\n<p>November 2010 &#8211; November 2013 Delegate, Chemical Society of Japan<\/p>\n<p>April 2011 &#8211; Present Full Member Representative, Chemical Society of Japan<\/p>\n<p>April 2012 &#8211; Present Secretary, Fullerene, Nanotube, and Graphene Society<\/p>\n<p>April 2014 &#8211; Present Committee Member, Industry-Academia Collaboration Committee, ATP Planning Subcommittee, Chemical Society of Japan<\/p>\n<p>January 2015 &#8211; Present Supervisor of the Experimental Classroom &#8220;Solar Cells&#8221;, Miraikan (National Museum of Emerging Science and Innovation)<\/p>\n<p>July 2012 &#8211; Present Editorial Board, Scientific Reports, Nature Publishing Group<\/p>\n<p>September 2015 &#8211; Present Vice President, Fullerene, Nanotube, and Graphene Society<\/p>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-695a444 elementor-widget elementor-widget-heading\" data-id=\"695a444\" data-element_type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Publications<\/h4>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-04d5a7d elementor-widget elementor-widget-html\" data-id=\"04d5a7d\" data-element_type=\"widget\" data-widget_type=\"html.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t<p>(1) Ligand Exchange Reactions of a 1,3-Butadiene Complex of Magnesium<\/p>\r\n<p>Kazushi Mashima, Yutaka Matsuo, Hiroki Fukumoto, Kazuhide Tani, Hajime Yasuda, and Akira Nakamura <em><\/em><\/p>\r\n<p><em>J. Organomet. Chem.<\/em> <strong>1997<\/strong>, <em>545\/546<\/em>, 549&ndash;552.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/S0022-328X(97)00380-X\" target=\"_blank\">DOI: 10.1016\/S0022-328X(97)00380-X<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) Nonplanar &sigma;<sup>2<\/sup>,&pi;- and Planar &sigma;<sup>2<\/sup>-Enediamide Coordinations of 1,4-Di(p-methoxyphenyl) -1,4-diaza-1,3-butadiene (= MeOC<sub>6<\/sub>H<sub>4<\/sub>-DAD) on Ta(&eta;<sup>5<\/sup>-C<sub>5<\/sub>R<sub>5<\/sub>) Fragments (R = H, Me): Crystal Structures of TaCl<sub>2<\/sub>(&sigma;<sup>2<\/sup>,&pi;-MeOC<sub>6<\/sub>H<sub>4<\/sub>-dad)(&eta;<sup>5<\/sup>-C<sub>5<\/sub>R<sub>5<\/sub>) and Ta(&sigma;<sup>2<\/sup>-MeOC<sub>6<\/sub>H<sub>4<\/sub>-dad)(&eta;<sup>5<\/sup>-C<sub>5<\/sub>Me<sub>5<\/sub>)(&eta;<sup>4<\/sup>-1,3-butadiene)<\/p>\r\n<p>Kazushi Mashima, Yutaka Matsuo, and Kazuhide Tani <em><\/em><\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>1997<\/strong>, 767&ndash;768.<\/p>\r\n<p>[<a href=\"https:\/\/doi.org\/10.1246\/cl.1997.767\" target=\"_blank\">DOI: 10.1246\/cl.1997.767<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) Oxidative Reaction of 1,5-Dithioniabicyclo[3.3.0]octane Bis(trifluoromethanesulfonate) with Diene Complexes of Zirconium and Tantalum: Synthesis of Cp<sub>2<\/sub>Zr(OTf)<sub>2<\/sub>(thf) and Cp(&eta;<sup>4<\/sup>-1,3-butadiene)Ta(OTf)<sub>2<\/sub><\/p>\r\n<p>Kazushi Mashima, Toshiyuki Oshiki, Yutaka Matsuo, and Kazuhide Tani<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>1997<\/strong>, 793&ndash;794.<\/p>\r\n<p>[<a href=\"https:\/\/doi.org\/10.1246\/cl.1997.793\" target=\"_blank\">DOI: 10.1246\/cl.1997.793<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) Polymerization of Methyl Methacrylate Catalyzed by Tantalum-diene Complexes, Ta(&eta;<sup>5<\/sup>-C<sub>5<\/sub>R<sub>5<\/sub>)(&eta;<sup>4<\/sup>-1,3-butadiene)<sub>2<\/sub> (R = H and Me), in the presence of cocatalyst AlMe(OC<sub>6<\/sub>H<sub>2<\/sub>-2,6-(tBu)<sub>2<\/sub>-4-Me)<sub>2<\/sub><\/p>\r\n<p>Kazushi Mashima, Yutaka Matsuo, and Kazuhide Tani<\/p>\r\n<p><em>Proc. Jpn. Acad., Ser. B<\/em> <strong>1998<\/strong>, <em>74<\/em>, 217&ndash;220.<\/p>\r\n<p>[<a href=\"https:\/\/doi.org\/10.2183\/pjab.74.217\" target=\"_blank\">DOI: 10.2183\/pjab.74.217<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(5) Unique Complexation of 1,4-Diaza-1,3-butadiene Ligand on Half-metallocene Fragments of Niobium and Tantalum<\/p>\r\n<p>Kazushi Mashima, Yutaka Matsuo, and Kazuhide Tani<\/p>\r\n<p><em>Organometallics<\/em> <strong>1999<\/strong>, <em>18<\/em>, 1471&ndash;1481.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/full\/10.1021\/om981003b\" target=\"_blank\">DOI: 10.1021\/om981003b<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(6) 1-Aza-1,3-butadiene Complexes of Tantalum: Preparation and Alkylation of TaCl<sub>2<\/sub>(&eta;<sup>5<\/sup>-C<sub>5<\/sub>Me<sub>5<\/sub>)(&eta;<sup>4<\/sup>-1-aza-1,3-butadiene)<\/p>\r\n<p>Kazushi Mashima, Yutaka Matsuo, Shinya Nakahara, and Kazuhide Tani<\/p>\r\n<p><em>J. Organomet. Chem.<\/em> <strong>2000<\/strong>, <em>593\/594<\/em>, 69&ndash;76.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/S0022-328X(99)00393-9\" target=\"_blank\">DOI: 10.1016\/S0022-328X(99)00393-9<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(7) Convenient Synthesis of Anionic Dinuclear Ruthenium(II) Complexes [NR<sub>2<\/sub>H<sub>2<\/sub>][{RuCl(diphosphine)}<sub>2<\/sub>(&mu;-Cl)<sub>3<\/sub>] [diphosphine = 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl, 2,2'-bis(di(p-tolyl)phosphino)-1,1'-binaphthyl, and 1,2-bis(diphenylphosphino)benzene]: Crystal Structure of [NEt<sub>2<\/sub>H<sub>2<\/sub>][{RuCl(1,2-bis(diphenylphosphino)benzene)}<sub>2<\/sub>(&mu;-Cl)<sub>3<\/sub>]<\/p>\r\n<p>Kazushi Mashima, Tomoko Nakamura, Yutaka Matsuo, and Kazuhide Tani<\/p>\r\n<p><em>J. Organomet. Chem.<\/em> <strong>2000<\/strong>, <em>607<\/em>, 51&ndash;56.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/S0022-328X(00)00192-3\" target=\"_blank\">DOI: 10.1016\/S0022-328X(00)00192-3<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(8) Synthesis and Characterization of Bis(iminopyrrolyl)zirconium Complexes<\/p>\r\n<p>Yutaka Matsuo, Kazushi Mashima, and Kazuhide Tani<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2000<\/strong>, 1114&ndash;1115.<\/p>\r\n<p>[<a href=\"https:\/\/doi.org\/10.1246\/cl.2000.1114\" target=\"_blank\">DOI: 10.1246\/cl.2000.1114<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(9) Half-metallocene Tantalum Complexes Bearing Methyl Methacrylate (MMA) and 1,4-Diaza-1,3-butadiene Ligands as MMA Polymerization Catalysts<\/p>\r\n<p>Yutaka Matsuo, Kazushi Mashima, and Kazuhide Tani<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2001<\/strong>, <em>40<\/em>, 960&ndash;962.<\/p>\r\n<p>[<a href=\"https:\/\/doi.org\/10.1002\/1521-3773(20010302)40:5&lt;960::AID-ANIE960&gt;3.0.CO;2-W\" target=\"_blank\">DOI: 10.1002\/1521-3773(20010302)40:5&lt;960::AID-ANIE960&gt;3.0.CO;2-W<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(10) Selective Formation of Homoleptic and Heteroleptic 2,5-Bis(N-aryliminomethyl)pyrrolyl Yttrium Complexes and Their Performance as Initiators of &epsilon;-Caprolactone Polymerization <br \/>Yutaka Matsuo, Kazushi Mashima, and Kazuhide Tani <br \/><em>Organometallics<\/em> <strong>2001<\/strong>, <em>20<\/em>, 3510&ndash;3518.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/om0101846\" target=\"_blank\">DOI: 10.1021\/om0101846<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(11) Intramolecular Coupling Reaction of 1-Aza-1,3-butadiene Ligand and Iminoacyl Ligand Giving Amido-Imido Complexes of Tantalum<\/p>\r\n<p>Yutaka Matsuo, Kazushi Mashima, and Kazuhide Tani<\/p>\r\n<p><em>Organometallics<\/em> <strong>2002<\/strong>, <em>21<\/em>, 138&ndash;143.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/om010724z\" target=\"_blank\">DOI: 10.1021\/om010724z<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(12) Half-metallocene 1-Aza-1,3-butadiene Complexes of Tantalum: Auxiliary Ligands on Tantalum Controlling Coordination Modes of the 1-Aza-1,3-butadiene Ligand<\/p>\r\n<p>Yutaka Matsuo, Kazushi Mashima, and Kazuhide Tani<\/p>\r\n<p><em>Bull. Chem. Soc. Jpn.<\/em> <strong>2002<\/strong>, <em>75<\/em>, 1291&ndash;1297.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1246\/bcsj.75.1291\" target=\"_blank\">DOI: 10.1246\/bcsj.75.1291<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(13) Cu(I)-Mediated Regioselective Tri-addition of Grignard Reagent to [70]Fullerene. Synthesis of Indenyl-type Metal Ligand Embedded into Graphitic Structure<\/p>\r\n<p>Masaya Sawamura, Motoki Toganoh, Hitoshi Iikura, Yutaka Matsuo, Atsushi Hirai, and Eiichi Nakamura<\/p>\r\n<p><em>J. Mater. Chem.<\/em> <strong>2002<\/strong>, <em>12<\/em>, 2109&ndash;2115.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1039\/b202130g\" target=\"_blank\">DOI: 10.1039\/b202130g<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(14) Hybrid of Ferrocene and Fullerene<\/p>\r\n<p>Masaya Sawamura, Yoichiro Kuninobu, Motoki Toganoh, Yutaka Matsuo, Masahiro Yamanaka, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2002<\/strong>, <em>124<\/em>, 9354&ndash;9355.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja026069j\" target=\"_blank\">DOI: 10.1021\/ja026069j<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(15) Stacking of Conical Molecules with a Fullerene Apex into Polar Columns in Crystals and Liquid crystals<\/p>\r\n<p>Masaya Sawamura, Kenji Kawai, Yutaka Matsuo, Kiyoshi Kanie, Takashi Kato, and Eiichi Nakamura<\/p>\r\n<p><em>Nature<\/em> <strong>2002<\/strong>, <em>419<\/em>, 702&ndash;705.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1038\/nature01110\" target=\"_blank\">DOI: 10.1038\/nature01110<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(16) Synthesis, Structure and Aromaticity of a Hoop-shaped Cyclic Benzenoid [10]Cyclophenacene<\/p>\r\n<p>Eiichi Nakamura, Kazukuni Tahara, Yutaka Matsuo, and Masaya Sawamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2003<\/strong>, <em>125<\/em>, 2834&ndash;2835.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja029915z\" target=\"_blank\">DOI: 10.1021\/ja029915z<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(17) Ruthenium (II) Complexes of Pentamethylated [60]Fullerene. Alkyl, Alkynyl, Chloro, Isocyanide, Phosphine Complexes<\/p>\r\n<p>Yutaka Matsuo and Eiichi Nakamura<\/p>\r\n<p><em>Organometallics<\/em> <strong>2003<\/strong>, <em>22<\/em>, 2554&ndash;2563.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/om0302387\" target=\"_blank\">DOI: 10.1021\/om0302387<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(18) Rhenium-templated Regioselective Polyhydrogenation of [60]Fullerene and Derivatives. Rhenium &eta;<sup>5<\/sup>-Complexes of Hydrofullerenes<\/p>\r\n<p>Motoki Toganoh, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2003<\/strong>, <em>42<\/em>, 3530&ndash;3532.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.200351722\" target=\"_blank\">DOI: 10.1002\/anie.200351722<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(19) Theoretical Studies on Structures and Reactivities of Finite-Length Single Wall Armchair Carbon Nanotubes <br \/>Yutaka Matsuo, Kazukuni Tahara, and Eiichi Nakamura <br \/><em>Org. Lett.<\/em> <strong>2003<\/strong>, <em>5<\/em>, 3181&ndash;3184.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ol0349514\" target=\"_blank\">DOI: 10.1021\/ol0349514<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(20) Synthesis and Structural Characterization of 2,5-Bis(N-aryliminomethyl)pyrrolyl Complexes of Aluminum<\/p>\r\n<p>Yutaka Matsuo, Hayato Tsurugi, Tsuneaki Yamagata, Kazuhide Tani, and Kazushi Mashima<\/p>\r\n<p><em>Bull. Chem. Soc. Jpn.<\/em> <strong>2003<\/strong>, <em>76<\/em>, 1965&ndash;1968.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1246\/bcsj.76.1965\" target=\"_blank\">DOI: 10.1246\/bcsj.76.1965<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(21) Synthesis and Catalytic Activity of Rhodium Diene Complexes Bearing Indenyl-Type Fullerene &eta;<sup>5<\/sup>-Ligand<\/p>\r\n<p>Motoki Toganoh, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Organomet. Chem.<\/em> <strong>2003<\/strong>, <em>683<\/em>, 295&ndash;300.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/S0022-328X(03)00465-0\" target=\"_blank\">DOI: 10.1016\/S0022-328X(03)00465-0<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(22) Synthesis of Ferrocene\/Hydrofullerene Hybrid and Functionalized Bucky Ferrocenes<\/p>\r\n<p>Motoki Toganoh, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2003<\/strong>, <em>125<\/em>, 13974&ndash;13975.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja037335b\" target=\"_blank\">DOI: 10.1021\/ja037335b<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(23) Synthesis and Reactivity of Bucky Ruthenocene Ru(&eta;<sup>5<\/sup>-C<sub>60<\/sub>Me<sub>5<\/sub>)(&eta;<sup>5<\/sup>-C<sub>5<\/sub>H<sub>5<\/sub>)<\/p>\r\n<p>Yutaka Matsuo, Yoichiro Kuninobu, Shingo Ito, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2004<\/strong>, <em>33<\/em>, 68&ndash;69.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1246\/cl.2004.68\" target=\"_blank\">DOI: 10.1246\/cl.2004.68<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(24) Stacking of Molecules Possessing a Fullerene Apex and a Cup-shaped Cavity Connected by Silicon-Connection<\/p>\r\n<p>Yutaka Matsuo, Ayako Muramatsu, Ryo Hamasaki, Norihiro Mizoshita, Takashi Kato, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2004<\/strong>, <em>126<\/em>, 432&ndash;433.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja038816y\" target=\"_blank\">DOI: 10.1021\/ja038816y<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(25) Synthesis of Functionalized Fullerene by Mono-alkylation of Fullerene Cyclopentadienide<\/p>\r\n<p>Ryo Hamasaki, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2004<\/strong>, <em>33<\/em>, 328&ndash;329.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1246\/cl.2004.328\" target=\"_blank\">DOI: 10.1246\/cl.2004.328<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(26) Intramolecular Benzylation of an Imino Group of Tridentate 2,5-Bis(N-aryliminomethyl)pyrrolyl Ligands Bound to Zirconium and Hafnium Gives Amido-Pyrrolyl Complexes That Catalyze Ethylene Polymerization<\/p>\r\n<p>Hayato Tsurugi, Yutaka Matsuo, Tsuneaki Yamagata, and Kazushi Mashima<\/p>\r\n<p><em>Organometallics<\/em> <strong>2004<\/strong>, <em>23<\/em>, 2797&ndash;2805.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/om049873i\" target=\"_blank\">DOI: 10.1021\/om049873i<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(27) Nickel, Palladium and Platinum Complexes of &eta;<sup>5<\/sup>-Cyclopentadienide C<sub>60<\/sub>R<sub>5<\/sub> Ligands. Kinetic and Thermodynamic Stabilization Effects of C<sub>60<\/sub>Ph<sub>5<\/sub> Ligand<\/p>\r\n<p>Yoichiro Kuninobu, Yutaka Matsuo, Motoki Toganoh, Masaya Sawamura, and Eiichi Nakamura<\/p>\r\n<p><em>Organometallics<\/em> <strong>2004<\/strong>, <em>23<\/em>, 3259&ndash;3266.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/om0499153\" target=\"_blank\">DOI: 10.1021\/om0499153<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(28) Creation of Hoop- and Bowl-Shaped Benzenoid Systems by Selective Detraction of [60]Fullerene Conjugation. [10]Cyclophenacene and Fused Corannulene Derivatives<\/p>\r\n<p>Yutaka Matsuo, Kazukuni Tahara, Masaya Sawamura, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2004<\/strong>, <em>126<\/em>, 8725&ndash;8734.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja048683w\" target=\"_blank\">DOI: 10.1021\/ja048683w<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(29) Molecular Orientation and Electronic Structure of Epitaxial Bucky Ferrocene (Fe(C<sub>60<\/sub>(CH<sub>3<\/sub>)<sub>5<\/sub>)C<sub>5<\/sub>H<sub>5<\/sub>) Thin Films<\/p>\r\n<p>Toshihiko Kaji, Toshihiro Shimada, Hiroaki Inoue, Yoichiro Kuninobu, Yutaka Matsuo, Eiichi Nakamura, and Koichiro Saiki<\/p>\r\n<p><em>J. Phys. Chem. B<\/em> <strong>2004<\/strong>, <em>108<\/em>, 9914&ndash;9918.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/jp037668v\" target=\"_blank\">DOI: 10.1021\/jp037668v<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(30) Photoinduced Change in the Raman Spectrum of Buckyferrocene (Fe(C<sub>60<\/sub>(CH<sub>3<\/sub>)<sub>5<\/sub>)C<sub>5<\/sub>H<sub>5<\/sub>)<\/p>\r\n<p>Toshihiro Shimada, Yoshiro Yamamoto, Toshihiko Kaji, Kenji Itaka, Hideomi Koinuma, Yoichiro Kuninobu, Yutaka Matsuo, Eiichi Nakamura, and Koichiro Saiki<\/p>\r\n<p><em>Solid State Commun.<\/em> <strong>2004<\/strong>, <em>132<\/em>, 197&ndash;201.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.ssc.2004.07.046\" target=\"_blank\">DOI: 10.1016\/j.ssc.2004.07.046<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(31) Electronic Structure of Stacked C<sub>60<\/sub> Shuttlecocks<\/p>\r\n<p>Susumu Okada, Ryotaro Arita, Yutaka Matsuo, Eiichi Nakamura, Atsushi Oshiyama, and Hideo Aoki<\/p>\r\n<p><em>Chem. Phys. Lett.<\/em> <strong>2004<\/strong>, <em>399<\/em>, 157&ndash;161.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.cplett.2004.09.152\" target=\"_blank\">DOI: 10.1016\/j.cplett.2004.09.152<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(32) Synthesis and Derivatization of Ir(I)- and Ir(III)-Pentamethyl[60]Fullerene Complexes<\/p>\r\n<p>Yutaka Matsuo, Akihiko Iwashita, and Eiichi Nakamura<\/p>\r\n<p><em>Organometallics<\/em> <strong>2005<\/strong>, <em>24<\/em>, 89&ndash;95.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/om049333l\" target=\"_blank\">DOI: 10.1021\/om049333l<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(33) Syntheses, Structure, and Derivatization of Potassium Complexes of Penta(organo)[60]fullerene-Monoanion, -Dianion, and -Trianion into Hepta- and Octa(organo)fullerenes<\/p>\r\n<p>Yutaka Matsuo and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2005<\/strong>, <em>127<\/em>, 8457&ndash;8466.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja050318x\" target=\"_blank\">DOI: 10.1021\/ja050318x<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(34) Ball-and-Socket Stacking of Supercharged Geodesic Polyarenes: Bonding by Interstitial Lithium Ions<\/p>\r\n<p>Ivan Aprahamian, David Eisenberg, Roy E. Hoffman, Tamar Sternfeld, Yutaka Matsuo, Edward A. Jackson, Eiichi Nakamura, Lawrence T. Scott, Tuvia Sheradsky, and Mordecai Rabinovitz<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2005<\/strong>, <em>127<\/em>, 9581&ndash;9587.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja0515102\" target=\"_blank\">DOI: 10.1021\/ja0515102<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(35) X-ray Crystallographic Characterization of Potassium Pentaphenyl[60]fullerene<\/p>\r\n<p>Yutaka Matsuo, Kazukuni Tahara, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2005<\/strong>, <em>34<\/em>, 1078&ndash;1079.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1246\/cl.2005.1078\" target=\"_blank\">DOI: 10.1246\/cl.2005.1078<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(36) M&ouml;ssbauer Spectroscopy of Bucky Ferrocenes: Lattice Dynamics and Motional Anisotropy of the Metal Atom<\/p>\r\n<p>Rolfe H. Herber, Israel Nowik, Yutaka Matsuo, Motoki Toganoh, Yoichiro Kuninobu, and Eiichi Nakamura<\/p>\r\n<p><em>Inorg. Chem.<\/em> <strong>2005<\/strong>, <em>44<\/em>, 5629&ndash;5635.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ic050251e\" target=\"_blank\">DOI: 10.1021\/ic050251e<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(37) Organic and Organometallic Derivatives of Dihydrogen-Encapsulated [60]Fullerene<\/p>\r\n<p>Yutaka Matsuo, Hiroyuki Isobe, Takatsugu Tanaka, Yasujiro Murata, Michihisa Murata, Koichi Komatsu, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2005<\/strong>, <em>127<\/em>, 17148&ndash;17149.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja056077a\" target=\"_blank\">DOI: 10.1021\/ja056077a<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(38) Synthesis of 6,9,12,15,18-Pentamethyl-1,6,9,12,15,18-Hexahydro(C<sub>60<\/sub>-<em>I<\/em><sub>h<\/sub>)[5,6]Fullerene<\/p>\r\n<p>Yutaka Matsuo, Ayako Muramatsu, Kazukuni Tahara, Madoka Koide, and Eiichi Nakamura; Checked by Peter Wipf and David L. Waller<\/p>\r\n<p><em>Org. Synth.<\/em> <strong>2006<\/strong>, <em>83<\/em>, 80&ndash;87.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(39) Synthesis of Trialkyl[60]fullerene C<sub>60<\/sub>(CH<sub>2<\/sub>SiMe<sub>3<\/sub>)<sub>3<\/sub>H and Its Potassium and Rhodium(I) Complexes<\/p>\r\n<p>Yutaka Matsuo and Eiichi Nakamura<\/p>\r\n<p><em>Inorg. Chim. Acta<\/em> <strong>2006<\/strong>, <em>359<\/em>, 1979&ndash;1982.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.ica.2005.07.021\" target=\"_blank\">DOI: 10.1016\/j.ica.2005.07.021<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(40) Convergent Synthesis of Polyfunctionalized Fullerene by Regioselective Five-fold Addition of Functionalized Organocopper Reagent to C<sub>60<\/sub><\/p>\r\n<p>Yu-Wu Zhong, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2006<\/strong>, <em>8<\/em>, 1463&ndash;1466.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ol060282t\" target=\"_blank\">DOI: 10.1021\/ol060282t<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(41) Remote Chirality Transfer within Coordination Sphere by the Use of a Ligand Possessing a Concave Cavity<\/p>\r\n<p>Yutaka Matsuo, Yuichi Mitani, Yu-Wu Zhong, and Eiichi Nakamura<\/p>\r\n<p><em>Organometallics<\/em> <strong>2006<\/strong>, <em>25<\/em>, 2826&ndash;2832.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/om060234c\" target=\"_blank\">DOI: 10.1021\/om060234c<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(42) Preparation and Characterization of Iminopyrrolyl Hafnium Complexes as Catalyst Precursors for &alpha;-Olefin Polymerization<\/p>\r\n<p>Hayato Tsurugi, Yutaka Matsuo, and Kazushi Mashima<\/p>\r\n<p><em>J. Mol. Catal. A: Chem.<\/em> <strong>2006<\/strong>, <em>254<\/em>, 131&ndash;137.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.molcata.2006.01.070\" target=\"_blank\">DOI: 10.1016\/j.molcata.2006.01.070<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(43) Synthesis and Electrochemistry of Double-decker Buckyferrocenes<\/p>\r\n<p>Yutaka Matsuo, Kazukuni Tahara, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2006<\/strong>, <em>128<\/em>, 7154&ndash;7155.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja061175x\" target=\"_blank\">DOI: 10.1021\/ja061175x<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(44) Sharing Orbitals -Ultrafast Excited State Deactivations with Different Outcome in Bucky Ferrocenes and Ruthenocenes<\/p>\r\n<p>Dirk M. Guldi, G. M. Aminur Rahman, Renata Marczak, Yutaka Matsuo, Masahiro Yamanaka, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2006<\/strong>, <em>128<\/em>, 9420&ndash;9427.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja061120v\" target=\"_blank\">DOI: 10.1021\/ja061120v<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(45) Synthesis, Structural, Electrochemical and Stacking Properties of Conical Molecules Possessing Buckyferrocene on Apex<\/p>\r\n<p>Yutaka Matsuo, Ayako Muramatsu, Yuko Kamikawa, Takashi Kato, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2006<\/strong>, <em>128<\/em>, 9586&ndash;9587.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja062757h\" target=\"_blank\">DOI: 10.1021\/ja062757h<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(46) Coupling of Alkylarene and Pentamethyl[60]fullerene by Iridium-catalyzed Benzylic C-H Bond Activation<\/p>\r\n<p>Yutaka Matsuo, Akihiko Iwashita, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2006<\/strong>, <em>35<\/em>, 858&ndash;859.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1246\/cl.2006.858\" target=\"_blank\">DOI: 10.1246\/cl.2006.858<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(47) Chiral Ruthenium Allenylidene Complexes Bearing a Fullerene Cyclopentadienyl Ligand: Synthesis, Characterization, and Remote Chirality Transfer<\/p>\r\n<p>Yu-Wu Zhong, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2007<\/strong>, <em>2<\/em>, 358&ndash;366.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.200600341\" target=\"_blank\">DOI: 10.1002\/asia.200600341<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(48) Regioselective Octa- and Deca-additions of Pyridine-modified Organocopper Reagent to [60]Fullerene<\/p>\r\n<p>Yutaka Matsuo, Kazukuni Tahara, Kouhei Morita, Keiko Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2007<\/strong>, <em>46<\/em>, 2844&ndash;2847.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.200604839\" target=\"_blank\">DOI: 10.1002\/anie.200604839<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(49) Lamellar Assembly of Conical Molecules Possessing a Fullerene Apex in Crystals and Liquid Crystals<\/p>\r\n<p>Yu-Wu Zhong, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2007<\/strong>, <em>129<\/em>, 3052&ndash;3053.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ja068780k\" target=\"_blank\">DOI: 10.1021\/ja068780k<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(50) AlCl<sub>3<\/sub>-Mediated Mono-, Di- and Tri-Hydroarylation of [60]fullerene<\/p>\r\n<p>Akihiko Iwashita, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2007<\/strong>, <em>46<\/em>, 3513&ndash;3516.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.200700062\" target=\"_blank\">DOI: 10.1002\/anie.200700062<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(51) Synthesis and Catalytic Activity of &eta;<sup>1<\/sup>-Allyl and &eta;<sup>3<\/sup>-Allyl, Ethyl, and Hydride Complexes of the Ruthenium-penta(methyl)[60]fullerene<\/p>\r\n<p>Yutaka Matsuo, Takashi Uematsu, and Eiichi Nakamura<\/p>\r\n<p><em>Eur. J. Inorg. Chem.<\/em> <strong>2007<\/strong>, 2729&ndash;2733.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/ejic.200700013\" target=\"_blank\">DOI: 10.1002\/ejic.200700013<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(52) Hoop-shaped Condensed Aromatic System: Synthesis and Structure of Iron- and Ruthenium-Hepta(organo)[60]fullerene Complexes<\/p>\r\n<p>Yutaka Matsuo, Takeshi Fujita, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2007<\/strong>, <em>2<\/em>, 948&ndash;955.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.200700124\" target=\"_blank\">DOI: 10.1002\/asia.200700124<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(53) New Fluorinated Channel-type Host Compounds<\/p>\r\n<p>Katharina Reichenb&auml;cher, Antonia Neels, Helen Stoeckli-Evans, Poonkodi Balasubramaniyan, Klaus M&uuml;ller, Yutaka Matsuo, Eiichi Nakamura, Edwin Weber, and J&uuml;rg Hulliger<\/p>\r\n<p><em>Cryst. Growth Des.<\/em> <strong>2007<\/strong>, <em>7<\/em>, 1399&ndash;1405.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/cg060682n\" target=\"_blank\">DOI: 10.1021\/cg060682n<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(54) Organic Photovoltaics Based on Solution-Processed Benzoporphyrin<br \/>Yoshiharu Sato, Takaaki Niinomi, Masahiko Hashiguchi, Yutaka Matsuo, and Eiichi Nakamura<br \/><em>Proc. SPIE<\/em> <strong>2007<\/strong>, <em>6656<\/em>, 66560U.<br \/>[<a href=\"http:\/\/dx.doi.org\/10.1117\/12.733804\" target=\"_blank\">DOI: 10.1117\/12.733804<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(55) Synthesis of <em>C<\/em><sub>5<\/sub>-symmetric Functionalized [60]Fullerenes by Copper-mediated Five-fold Addition of Reformatsky Reagents<\/p>\r\n<p>Takahiro Nakae, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2008<\/strong>, <em>10<\/em>, 621&ndash;623.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ol702874w\" target=\"_blank\">DOI: 10.1021\/ol702874w<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(56) Addition of Tetrahydrofuran to [60]Fullerene through C-H Bond Activation Induced by Arylzinc Reagents<\/p>\r\n<p>Yutaka Matsuo, Ying Zhang, and Eiichi Nakamura<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2008<\/strong>, <em>10<\/em>, 1251&ndash;1254.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/ol800143b\" target=\"_blank\">DOI: 10.1021\/ol800143b<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(57) Ruthenium Connection in Fullerene-Ferrocene Arrays. Synthesis of Ru(C<sub>60<\/sub>Me<sub>5<\/sub>)R(CO)<sub>2<\/sub> (R = C<sub>6<\/sub>H<sub>4<\/sub>Fc and CCFc) and Their Charge Transfer Properties<\/p>\r\n<p>Yutaka Matsuo, Keiko Matsuo, Takeshi Nanao, Renata Marczak, S. Shankara Gayathri, Dirk M. Guldi, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2008<\/strong>, <em>3<\/em>, 841&ndash;848.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.200700379\" target=\"_blank\">DOI: 10.1002\/asia.200700379<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(58) Photocurrent-Generating Properties of Organometallic Fullerene Molecules on an Electrode<\/p>\r\n<p>Yutaka Matsuo, Katsuhiko Kanaizuka, Keiko Matsuo, Yu-Wu Zhong, Takahiro Nakae, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2008<\/strong>, <em>130<\/em>, 5016&ndash;5017.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja800481d\" target=\"_blank\">DOI: 10.1021\/ja800481d<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(59) Synthesis of Metal Fullerene Complexes by the Use of Fullerene Halides<\/p>\r\n<p>Yutaka Matsuo, Yoichiro Kuninobu, Ayako Muramatsu, Masaya Sawamura, and Eiichi Nakamura<\/p>\r\n<p><em>Organometallics<\/em> <strong>2008<\/strong>, <em>27<\/em>, 3403&ndash;3409.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1021\/om8001262\" target=\"_blank\">DOI: 10.1021\/om8001262<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(60) Group 6 Metal Complexes of the &eta;<sup>5<\/sup>-Pentamethyl[60]fullerene<\/p>\r\n<p>Yutaka Matsuo, Akihiko Iwashita, and Eiichi Nakamura<\/p>\r\n<p><em>Organometallics<\/em> <strong>2008<\/strong>, <em>27<\/em>, 4611&ndash;4617.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/om800308n\" target=\"_blank\">DOI: 10.1021\/om800308n<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(61) Penta(pyrenyl)[60]fullerenes. Pyrene-Pyrene and [60]Fullerene-Pyrene Interactions in Crystal and in Solution<\/p>\r\n<p>Yutaka Matsuo, Kouhei Morita, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2008<\/strong>, <em>8<\/em>, 1350&ndash;1357. (Noyori special issue)<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.200800122\" target=\"_blank\">DOI: 10.1002\/asia.200800122<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(62) Light Emission of [10]Cyclophenacene through Energy Transfer from Neighboring Carbazolylphenyl Dendrons<\/p>\r\n<p>Xiaoyong Zhang, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2008<\/strong>, <em>10<\/em>, 4145&ndash;4147.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol8017193\" target=\"_blank\">DOI: 10.1021\/ol8017193<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(63) Regioselective Synthesis of 1,4-Di(organo)[60]fullerenes through DMF-assisted Mono-addition of Silylmethyl Grignard Reagents and Subsequent Alkylation Reaction<\/p>\r\n<p>Yutaka Matsuo, Akihiko Iwashita, Yoko Abe, Chang-Zhi Li, Keiko Matsuo, Masahiko Hashiguchi, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2008<\/strong>, <em>130<\/em>, 15429&ndash;15436.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja8041299\" target=\"_blank\">DOI: 10.1021\/ja8041299<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(64) Uniquely Shaped Double-Decker Buckyferrocenes - Distinct Electron Donor-Acceptor Interactions<\/p>\r\n<p>Renata Marczak, Mateusz Wielopolski, S. Shankara Gayathri, Dirk M. Guldi, Yutaka Matsuo, Keiko Matsuo, Kazukuni Tahara, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2008<\/strong>, <em>130<\/em>, 16207&ndash;16215.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja8013902\" target=\"_blank\">DOI: 10.1021\/ja8013902<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(65) Organic photovoltaic cell based on benzoporphyrin with p-i-n junction<\/p>\r\n<p>Yoshiharu Sato, Takaaki Niinomi, Yoko Abe, Yutaka Matsuo, Eiichi Nakamura<\/p>\r\n<p><em>Proceedings of SPIE<\/em>, <strong>2008<\/strong>, 7052, 70520J.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(66) Iron and Ruthenium Nanoparticles in Carbon Prepared by Thermolysis of Buckymetallocenes<\/p>\r\n<p>Takahiro Nakae, Yutaka Matsuo, Masatoshi Takagi, Yuta Sato, Kazu Suenaga, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2009<\/strong>, <em>4<\/em>, 457&ndash;465.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.200800331\" target=\"_blank\">DOI: 10.1002\/asia.200800331<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(67) Synthesis, Electrochemical and Photophysical Properties, and Electroluminescent Performance of the Octa- and Deca-aryl [60]Fullerene Derivatives<\/p>\r\n<p>Yutaka Matsuo, Yoshiharu Sato, Masahiko Hashiguchi, Keiko Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Adv. Funct. Mater.<\/em> <strong>2009<\/strong>, <em>19<\/em>, 2224&ndash;2229.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1002\/adfm.200900021\" target=\"_blank\">DOI: 10.1002\/adfm.200900021<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(68) Ring-opening Reaction of Tetrahydrofuran on the Penta(organo)[60]fullerenes: Synthesis of Hydroxybutyl, Methacrylate, and Norbornene Derivatives<\/p>\r\n<p>Yutaka Matsuo, Akihiko Iwashita, Hiromi Oyama, and Eiichi Nakamura<\/p>\r\n<p><em>Tetrahedron Lett.<\/em> <strong>2009<\/strong>, <em>50<\/em>, 3411&ndash;3413. (50th Anniversary of TL)<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2009.02.155\" target=\"_blank\">DOI: 10.1016\/j.tetlet.2009.02.155<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(69) Random Telegraphic Conductance Fluctuation at Au-Pentacene-Au Nanojunctions<\/p>\r\n<p>Yuki Kihira, Toshihiro Shimada, Yutaka Matsuo, Eiichi Nakamura, and Tetsuya Hasegawa<\/p>\r\n<p><em>Nano Lett.<\/em> <strong>2009<\/strong>, <em>9<\/em>, 1442&ndash;1446.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/nl803284t\" target=\"_blank\">DOI: 10.1021\/nl803284t<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(70) Penta(organo)[60]fullerenes as Acceptors for Organic Photovoltaic Cells<\/p>\r\n<p>Takaaki Niinomi, Yutaka Matsuo, Masahiko Hashiguchi, Yoshiharu Sato, and Eiichi Nakamura<\/p>\r\n<p><em>J. Mater. Chem.<\/em> <strong>2009<\/strong>, <em>19<\/em>, 5804&ndash;5811.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2009\/JM\/b904485j\" target=\"_blank\">DOI: 10.1039\/b904485j<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(71) Efficient Bidirectional Photocurrent Generation by Self-assembled Monolayer of Penta(aryl)[60]fullerene Phosphonic Acid<\/p>\r\n<p>Aiko Sakamoto, Yutaka Matsuo, Keiko Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2009<\/strong>, <em>4<\/em>, 1208&ndash;1212.<\/p>\r\n<p>[<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.200900155\/abstract\" target=\"_blank\">DOI: 10.1002\/asia.200900155<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(72) Di- and Trinuclear [70]Fullerene Complexes: Syntheses and Metal-Metal Electronic Interactions<\/p>\r\n<p>Yutaka Matsuo, Kazukuni Tahara, Takeshi Fujita, and Eiichi Nakamura<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2009<\/strong>, <em>48<\/em>, 6239&ndash;6241.<\/p>\r\n<p>[<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200902185\/abstract\" target=\"_blank\">DOI: 10.1002\/anie.200902185<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(73) &pi;-Conjugated Multi-Donor\/Acceptor Arrays of Fullerene-Cobaltadithiolene-Tetrathiafulvalene: From Synthesis and Structure to Electronic Interactions<\/p>\r\n<p>Yutaka Matsuo, Masashi Maruyama, S. Shankara Gayathri, Tomoya Uchida, Dirk M. Guldi, Hideo Kishida, Arao Nakamura, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2009<\/strong>, <em>131<\/em>, 12643&ndash;12649.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/full\/10.1021\/ja902312q\" target=\"_blank\">DOI: 10.1021\/ja902312q<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(74) Synthesis of Imino[60]fullerenes Using Nitriles and Trimethylsilylmethyl Triflate<\/p>\r\n<p>Keiko Matsuo, Yutaka Matsuo, Akihiko Iwashita, and Eiichi Nakamura<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2009<\/strong>, <em>11<\/em>, 4192&ndash;4194.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/full\/10.1021\/ol901851g\" target=\"_blank\">DOI: 10.1021\/ol901851g<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(75) Columnar Structure in Bulk Heterojunction in Solution-processable Three-layered p-i-n Organic Photovoltaic Devices Using Tetrabenzoporphyrin Precursor and Silylmethyl[60]fullerene<\/p>\r\n<p>Yutaka Matsuo, Yoshiharu Sato, Takaaki Niinomi, Iwao Soga, Hideyuki Tanaka, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2009<\/strong>, <em>131<\/em>, 16048&ndash;16050.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja9048702\" target=\"_blank\">DOI: 10.1021\/ja9048702<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(76) Luminescent Bow-tie-shaped Decaaryl[60]fullerene Mesogens<\/p>\r\n<p>Chang-Zhi Li, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2009<\/strong>, <em>131<\/em>, 17058&ndash;17059.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja907908m\" target=\"_blank\">DOI: 10.1021\/ja907908m<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(77) Substituent-Dependent Ordering of Adlayer Structures of Fullerene Derivatives: A Scanning Tunneling Microscopy Study<\/p>\r\n<p>Ting Chen, Ge-Bo Pan, Hui-Juan Yan, Li-Jun Wan, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Phys. Chem. C<\/em> <strong>2010<\/strong>, <em>114<\/em>, 3170&ndash;3174.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jp9114173\" target=\"_blank\">DOI: 10.1021\/jp9114173<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(78) Highly Soluble Penta[(alkyl)dimethylsilylmethyl][60]fullerenes and Their Ruthenium and Palladium Complexes<\/p>\r\n<p>Yutaka Matsuo, Ayako Muramatsu, Jiang Lu, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2010<\/strong>, <em>39<\/em>, 342&ndash;343.<\/p>\r\n<p>[<a href=\"http:\/\/www.jstage.jst.go.jp\/article\/cl\/39\/4\/39_342\/_article\" target=\"_blank\">DOI: 10.1246\/cl.2010.342<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(79) Reductive Benzylation of Dimetallo Hexaaryl[70]fullerenes on the Equatorial Region<\/p>\r\n<p>Takeshi Fujita, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2010<\/strong>, <em>5<\/em>, 835&ndash;840.<\/p>\r\n<p>[<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.200900651\/abstract\" target=\"_blank\">DOI: 10.1002\/asia.200900651<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(80) C<sub>60<\/sub> Derivatives Having Self-Assembly Capability<\/p>\r\n<p>Yutaka Matsuo<\/p>\r\n<p><em>Fullerene, Nanotubes, and Carbon Nanostructures<\/em> <strong>2010<\/strong>, <em>18<\/em>, 338&ndash;352.<\/p>\r\n<p>[<a href=\"http:\/\/www.informaworld.com\/smpp\/content~db=all~content=a928677994\" target=\"_blank\">DOI: 10.1080\/1536383X.2010.487395<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(81) Synthesis of Ruthenium Pentamethyl[60]fullerene Complexes bearing Monodentate Diphosphino-methane, -ferrocene, and -butane Ligands<\/p>\r\n<p>Yutaka Matsuo, Bo Keun Park, Yuichi Mitani, Yu-Wu Zhong, Masashi Maruyama, and Eiichi Nakamura<\/p>\r\n<p><em>Bull. Korean Chem. Soc.<\/em> <strong>2010<\/strong>, <em>31<\/em>, 697&ndash;699.<\/p>\r\n<p>[<a href=\"http:\/\/newjournal.kcsnet.or.kr\/main\/j_search\/j_abstract_view.htm?code=B100337&amp;qpage=j_search&amp;spage=b_bkcs&amp;dpage=ar\" target=\"_blank\">DOI: 10.5012\/bkcs.2010.31.03.697<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(82) Loading Pentapod Deca(organo)[60]fullerenes with Electron Donors: From Photophysics to Photoelectrochemical Bilayers<\/p>\r\n<p>Yutaka Matsuo, Takahiko Ichiki, Shankara Gayathri Radhakrishnan, Dirk M. Guldi, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2010<\/strong>, <em>132<\/em>, 6342&ndash;6348.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja909970h\" target=\"_blank\">DOI: 10.1021\/ja909970h<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(83) Copper-catalyzed Formal [4+2] Annulation between Alkyne and Fullerene Bromide<\/p>\r\n<p>Zuo Xiao, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2010<\/strong>, <em>132<\/em>, 12234&ndash;12236.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja1056399\" target=\"_blank\">DOI: 10.1021\/ja1056399<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(84) Voltammetry of Half-Sandwich Manganese Group Complexes of &eta;<sup>6<\/sup>-PhC<sub>3<\/sub>B<sub>7<\/sub>H<sub>9<\/sub> and &eta;<sup>5<\/sup>-C<sub>60<\/sub>Bn<sub>2<\/sub>PhH<sub>2<\/sub>, Two Ligands That Are Cyclopentadienyl Mimicks<\/p>\r\n<p>Michael P. Stewart, Robert Butterick III, Larry G. Sneddon, Yutaka Matsuo, and William E. Geiger<\/p>\r\n<p><em>Inorg. Chim. Acta.<\/em> <strong>2010<\/strong>, <em>364<\/em>, 251&ndash;254.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.ica.2010.05.040\" target=\"_blank\">DOI: 10.1016\/j.ica.2010.05.040<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(85) Conical Pentaaryl[60]Fullerene Thiols: Self-Assembled Monolayers on Gold and Photocurrent Generating Property<\/p>\r\n<p>Yutaka Matsuo, Sebastian Lacher, Aiko Sakamoto, Keiko Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Phys. Chem. C<\/em> <strong>2010<\/strong>, <em>114<\/em>, 17741&ndash;17752.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jp1059402\" target=\"_blank\">DOI: 10.1021\/jp1059402<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(86) Face-to-face C<sub>6<\/sub>F<sub>5<\/sub>-[60]Fullerene Interaction for Ordering Fullerene Molecules and Application to Thin-film Organic Photovoltaics<\/p>\r\n<p>Chang-Zhi Li, Yutaka Matsuo, Takaaki Niinomi, Yoshiharu Sato, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2010<\/strong>, <em>46<\/em>, 8582&ndash;8584.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2010\/CC\/C0CC03028G\" target=\"_blank\">DOI: 10.1039\/C0CC03028G<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(87) Octupole-like Supramolecular Aggregates of Conical Iron Fullerene Complexes into a Three-Dimensional Liquid Crystalline Lattice<\/p>\r\n<p>Chang-Zhi Li, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2010<\/strong>, <em>132<\/em>, 15514&ndash;15515.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja1073933\" target=\"_blank\">DOI: 10.1021\/ja1073933<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(88) Simple Formation of C<sub>60<\/sub> and C<sub>60<\/sub>-Ferrocene Conjugated Monolayers Anchored onto Silicon Oxide with Five Carboxylic Acids and Their Transistor Applications<\/p>\r\n<p>Yoshimitsu Itoh, Bumjung Kim, Raluca I. Gearba, Noah J. Tremblay, Ron Pindak, Yutaka Matsuo, Eiichi Nakamura, and Colin Nuckolls<\/p>\r\n<p><em>Chem. Mater.<\/em> <strong>2011<\/strong>, <em>23<\/em>, 970&ndash;975.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm1025975\" target=\"_blank\">DOI: 10.1021\/cm1025975<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(89) Synthesis of 1,4-Diaryl[60]fullerenes by Bis-hydroarylation of C<sub>60<\/sub> and Their Use in Solution-processable, Thin-film Organic Photovoltaic Cells<\/p>\r\n<p>Yutaka Matsuo, Ying Zhang, Iwao Soga, Yoshiharu Sato, and Eiichi Nakamura<\/p>\r\n<p><em>Tetrahedron Lett.<\/em> <strong>2011<\/strong>, <em>52<\/em>, 2240&ndash;2242.<\/p>\r\n<p>[<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2011.01.031\" target=\"_blank\">DOI:10.1016\/j.tetlet.2011.01.031<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(90) Aryl-Perfluoroaryl Substituted Tetracene: Induction of Face-to-Face &pi;-&pi; Stacking and Enhancement of Charge Carrier Properties<\/p>\r\n<p>Toshihiro Okamoto, Katsumasa Nakahara, Akinori Saeki, Shu Seki,&nbsp;Joon Hak Oh, Hylke B. Akkerman, Zhenan Bao, and Yutaka Matsuo<\/p>\r\n<p><em>Chem. Mater.<\/em> <strong>2011<\/strong>, <em>23<\/em>, 1646&ndash;1649.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm200356y\" target=\"_blank\">DOI: 10.1021\/cm200356y<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(91) Isolation of Planar 4-Membered Aromatic Systems by Using Confined Spaces of Cobalt Pentaaryl[60]fullerene Complexes<\/p>\r\n<p>Masashi Maruyama, Jing-Dong Guo, Shigeru Nagase, Eiichi Nakamura, and Yutaka Matsuo<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2011<\/strong>, <em>133<\/em>, 6890&ndash;6893.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja111474v\" target=\"_blank\">DOI: 10.1021\/ja111474v<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(92) A Scalable Synthesis of Methano[60]fullerene and Congeners by the Oxidative Cyclopropanation Reaction of Silylmethylfullerene<\/p>\r\n<p>Ying Zhang, Yutaka Matsuo, Chang-Zhi Li, Hideyuki Tanaka, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2011<\/strong>, <em>133<\/em>, 8086&ndash;8089.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja201267t\" target=\"_blank\">DOI: 10.1021\/ja201267t<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(93) Molecular Photoelectric Switch Using a Mixed SAM of Organic [60]Fullerene and [70]Fullerene Doped with a Single Iron Atom<\/p>\r\n<p>Yutaka Matsuo, Takahiko Ichiki, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2011<\/strong>, <em>133<\/em>, 9932&ndash;9937.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja203224d\" target=\"_blank\">DOI: 10.1021\/ja203224d<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(94) Synthesis, Physical Properties, and Crystal Structure of Acetetracenylene-1,2-dione<\/p>\r\n<p>Toshihiro Okamoto, Tsuyoshi Suzuki, Shungo Kojima, and Yutaka Matsuo<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2011<\/strong>, <em>40<\/em>, 739&ndash;741.<\/p>\r\n<p>[<a href=\"http:\/\/www.jstage.jst.go.jp\/article\/cl\/40\/7\/40_739\/_article\" target=\"_blank\">DOI: 10.1246\/cl.2011.739<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(95) Facile Fullerene Modification: FeCl<sub>3<\/sub>-mediated Quantitative Conversion of C<sub>60<\/sub> to Polyarylated Fullerenes Containing Pentaaryl(chloro)[60]fullerenes<\/p>\r\n<p>Masahiko Hashiguchi, Kazuhiro Watanabe and Yutaka Matsuo<\/p>\r\n<p><em>Org. Biomol. Chem.<\/em> <strong>2011<\/strong>, <em>9<\/em>, 6417&ndash;6421.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2011\/OB\/C1OB05895A\" target=\"_blank\">DOI: 10.1039\/C1OB05895A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(96) Facile Synthesis of a 56&pi;-electron 1,2-Dihydromethano-[60]PCBM and Its Application for Thermally Stable Polymer Solar Cells<\/p>\r\n<p>Chang-Zhi Li, Shang-Chieh Chien, Hin-Lap Yip, Chu-Chen Chueh, Fang-Chung Chen, Yutaka Matsuo, Eiichi Nakamura and Alex K.-Y. Jen<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2011<\/strong>, <em>47<\/em>, 10082&ndash;10084.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2011\/CC\/c1cc14446d\" target=\"_blank\">DOI: 10.1039\/C1CC14446D<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(97) Regioselective Synthesis of Tetra(aryl)-Mono(silylmethyl)[60]fullerenes and Derivatization to Methanofullerene Compound<\/p>\r\n<p>Chang-Zhi Li, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Tetrahedron<\/em> <strong>2011<\/strong>, <em>67<\/em>, 9944&ndash;9949.<\/p>\r\n<p>[<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402011015079\" target=\"_blank\">DOI:10.1016\/j.tet.2011.09.125<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(98) Electron Microscopic Imaging of a Single Group 8 Metal Atom Catalyzing C-C Bond Reorganization of Fullerenes<\/p>\r\n<p>Eiichi Nakamura, Masanori Koshino, Takeshi Saito, Yoshiko Niimi, Kazu Suenaga, and Yutaka Matsuo<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2011<\/strong>, <em>133<\/em>, 14151&ndash;14153.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja203225n\" target=\"_blank\">DOI: 10.1021\/ja203225n<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(99) Molecular and Supramolecular Control of the Work Function of an Inorganic Electrode with Self-assembled Umbrella-shaped Fullerene Derivatives<\/p>\r\n<p>Sebastian Lacher, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2011<\/strong>, <em>133<\/em>, 16997&ndash;17004.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja2067675\" target=\"_blank\">DOI: 10.1021\/ja206767<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(100) Electric Field Dependent Photocurrent Generation in a Thin-film Organic Photovoltaic Device with a [70]Fullerene&ndash;benzodifuranone Dyad<\/p>\r\n<p>Pirmin A. Ulmann, Hideyuki Tanaka, Yutaka Matsuo, Zuo Xiao, Iwao Soga, and Eiichi Nakamura<\/p>\r\n<p><em>Phys. Chem. Chem. Phys.<\/em> <strong>2011<\/strong>, <em>13<\/em>, 21045&ndash;21049.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2011\/cp\/c1cp22886b\" target=\"_blank\">DOI: 10.1039\/C1CP22886B<\/a>]<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<p>(101) Regiocontrolled Synthesis of 1,2-Di(organo)fullerenes via Copper-Assisted 1,4-Aryl Migration from Silicon to Carbon<\/p>\r\n<p>Ying Zhang, Yutaka Matsuo, and Eiichi Nakamura<em><\/em><\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2011<\/strong>, <em>13<\/em>, 6058&ndash;6061.<\/p>\r\n<p>[<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol202511u\" target=\"_blank\">DOI: 10.1021\/ol202511u<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(102) Small-Molecule-Based Organic Photovoltaic Devices Covering Visible and Near-Infrared Absorption through Phase Transition of Titanylphthalocyanine Induced by Solvent Exposure<\/p>\r\n<p>Naoki Obata, Yoshiharu Sato, Eiichi Nakamura, and Yutaka Matsuo<\/p>\r\n<p><em>Jpn. J. Appl. Phys.<\/em> <strong>2011<\/strong>, <em>50<\/em>, 121603.<\/p>\r\n<p>[<a href=\"http:\/\/jjap.jsap.jp\/link?JJAP\/50\/121603\/\" target=\"_blank\">DOI: 10.1143\/JJAP.50.121603<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(103) Construction of Long-Wavelength-Light&nbsp;Photocurrent Generation System Based on Self-Assembled Monolayer of&nbsp;Cobaltadithiolene [60]Fullerene Complex<\/p>\r\n<p>Yutaka Matsuo and&nbsp;Masashi Maruyama<\/p>\r\n<p><em>J. Nanosci. Nanotech.<\/em><strong><\/strong> <strong>2012<\/strong>, <em>12<\/em>, 6869&ndash;6871. (ANM2010 special issue)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(104) Tetracene Dicarboxylic Imide and Its Disulfide: Synthesis of New Ambipolar Organic Semiconductors for Organic Photovoltaic Cells<\/p>\r\n<p>Toshihiro Okamoto, Tsuyoshi Suzuki, Hideyuki Tanaka, Daisuke Hashizume, and Yutaka Matsuo<em><\/em><\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2012<\/strong>, <em>7<\/em>, 105&ndash;111. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201100590\/abstract\" target=\"_blank\">DOI: 10.1002\/asia.201100590<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(105) Role of Subsurface Diffusion and Ostwald Ripening in Catalyst Formation for SWNT Forest Growth<\/p>\r\n<p>Shunsuke Sakurai, Hidekazu Nishino, Don N. Futaba, Satoshi Yasuda, Takeo Yamada, Alan Maigne, Yutaka Matsuo, Eiichi Nakamura, Motoo Yumura, and Kenji Hata<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2012<\/strong>, <em>134<\/em>, 2148&ndash;2153. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja208706c\" target=\"_blank\">DOI: 10.1021\/ja208706c<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(106) Fullerene Acceptor for Improving Open-Circuit Voltage in Inverted Organic Photovoltaic Devices without Accompanying Decrease in Short-Circuit Current Density<\/p>\r\n<p>Yutaka Matsuo, Junichi Hatano, Takayuki Kuwabara, and Kohshin Takahashi<\/p>\r\n<p><em>Appl. Phys. Lett.<\/em> <strong>2012<\/strong>, <em>100<\/em>, 063303. [<a href=\"http:\/\/dx.doi.org\/10.1063\/1.3683469\" target=\"_blank\">DOI: 10.1063\/1.3683469<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(107) Development of Fullerene Derivatives with High LUMO Level through Changes in &pi;-Conjugated System Shape<\/p>\r\n<p>Yutaka Matsuo<\/p>\r\n<p><em>Pure Appl. Chem.<\/em> <strong>2012<\/strong>, <em>84<\/em>, 945&ndash;952 (ISNA-14 special issue). [<a href=\"http:\/\/iupac.org\/publications\/pac\/84\/4\/0945\/\" target=\"_blank\">DOI: 10.1351\/PAC-CON-11-11-01<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(108) Development of New Fullerene-based Electron Acceptors for Efficient Organic Photovoltaic Cells<\/p>\r\n<p>Yutaka Matsuo<\/p>\r\n<p><em>Proc. MRS<\/em> <strong>2012<\/strong>, <em>1390<\/em>, mrsf11-1390-h13-79. [DOI: 10.1557\/opl.2012.652]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(109) Facile Synthesis of Biphenyl-Fused BODIPY and Its Property<\/p>\r\n<p>Yosuke Hayashi, Naoki Obata, Masatomo Tamaru, Shigeru Yamaguchi, Yutaka Matsuo, Akinori Saeki, Shu Seki, Yuka Kureishi, Shohei Saito, Shigehiro Yamaguchi, and Hiroshi Shinokubo<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2012<\/strong>, <em>14<\/em>, 866&ndash;869. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol2033916\" target=\"_blank\">DOI: 10.1021\/ol2033916<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(110) Deterioration of Bulk Heterojunction Organic Photovoltaic Devices by a Minute Amount of Oxidized Fullerene<\/p>\r\n<p>Yutaka Matsuo, Ayako Ozu, Naoki Obata, Naoya Fukuda, Hideyuki Tanaka, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2012<\/strong>, <em>48<\/em>, 3878&ndash;3880. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2012\/CC\/c2cc30262d\" target=\"_blank\">DOI: 10.1039\/C2CC30262D<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(111) Facile Purification of C<sub>60<\/sub>O-containing [60]Fullerene Using Trialkylphosphines at Room Temperature<\/p>\r\n<p>Masahiko Hashiguchi, Koichi Nagata, Katsutomo Tanaka, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Process Res. Dev.<\/em> <strong>2012<\/strong>, <em>16,<\/em> 643&ndash;646. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/op200376w\" target=\"_blank\">DOI: 10.1021\/op200376w<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(112) An Amorphous Mesophase Generated by Thermal Annealing for High-Performance Organic Photovoltaic Devices<\/p>\r\n<p>Hideyuki Tanaka, Yoko Abe, Yutaka Matsuo, Junya Kawai, Iwao Soga, Yoshiharu Sato, and Eiichi Nakamura<\/p>\r\n<p><em>Adv. Mater.<\/em> <strong>2012<\/strong>, <em>24<\/em>, 3521&ndash;3525. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adma.201200490\/abstract\" target=\"_blank\">DOI: 10.1002\/adma.201200490<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(113) FeCl<sub>3<\/sub>-mediated Synthesis of Fullerenyl Esters as Low-LUMO Acceptors for Organic Photovoltaic Devices<\/p>\r\n<p>Masahiko Hashiguchi, Naoki Obata, Masashi Maruyama, Kee Sheng Yeo, Takao Ueno, Tomohiko Ikebe, Isao Takahashi, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2012<\/strong>, <em>14<\/em>, 3276&ndash;3279. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol301186u\" target=\"_blank\">DOI:10.1021\/ol301186u<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(114) Structurally Defined High-LUMO-level 66&pi;-[70]Fullerene Derivatives: Synthesis and Application in Organic Photovoltaic Cells<\/p>\r\n<p>Zuo Xiao, Yutaka Matsuo, Iwao Soga, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Mater.<\/em> <strong>2012<\/strong>, <em>24<\/em>, 2572&ndash;2582. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm301238n\" target=\"_blank\">DOI: 10.1021\/cm301238n<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(115) Electropolymerized Conjugated Polyelectrolytes with Tunable Work Function and Hydrophobicity as an Anode Buffer in Organic Optoelectronics<\/p>\r\n<p>Sebastian Lacher, Naoki Obata, Shyh-Chyang Luo, Yutaka Matsuo, Bo Zhu, Hsiao-hua Yu, and Eiichi Nakamura<\/p>\r\n<p><em>ACS Appl. Mater. Interfaces<\/em> <strong>2012<\/strong>, <em>4<\/em>, 3396&ndash;3404. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/am300366d\" target=\"_blank\">DOI: 10.1021\/am300366d<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(116) Covalently Chemical Modification of Lithium Ion-Encapsulated Fullerene: Synthesis and Characterization of [Li<sup>+<\/sup>@PCBM]PF<sub>6<\/sub><sup>&ndash;<\/sup><\/p>\r\n<p>Yutaka Matsuo, Hiroshi Okada, Masashi Maruyama, Hiroyasu Sato, Hiromi Tobita, Yoshihiro Ono, Kenji Omote, Kazuhiko Kawachi, and Yasuhiko Kasama<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2012<\/strong>, <em>14<\/em>, 3784&ndash;3787. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol301671n\" target=\"_blank\">DOI: 10.1021\/ol301671n<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(117) Soluble Porphyrin Donors for Small Molecule Bulk Heterojunction Solar Cells<\/p>\r\n<p>Junichi Hatano, Naoki Obata, Shigeru Yamaguchi, Takeshi Yasuda, and Yutaka Matsuo<\/p>\r\n<p><em>J. Mater. Chem.<\/em> <strong>2012<\/strong>, <em>22<\/em>, 19258&ndash;19263. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2012\/JM\/c2jm33956k\">DOI: 10.1039\/C2JM33956K<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(118) Benzo[<em>c<\/em>]thiophene-C<sub>60<\/sub> Diadduct: An Electron Acceptor for p&ndash;n Junction Organic Solar Cells Harvesting Visible to Near-IR Light<\/p>\r\n<p>Yonggang Zhen, Naoki Obata, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2012<\/strong>, <em>7<\/em>, 2644&ndash;2649. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201200698\/abstract\" target=\"_blank\">DOI: 10.1002\/asia.201200698<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(119) Preparation of Li-encapsulated [60]Fullerene (Li@C<sub>60<\/sub>) and Its Derivatization to Hexafluorophosphate&ndash; Salt [Li<sup>+<\/sup>@C<sub>60<\/sub>]PF<sub>6<\/sub><sup>&ndash;<\/sup><\/p>\r\n<p>Hiroshi Okada, Takashi Komuro, Takeshi Sakai, Yutaka Matsuo, Yoshihiro Ono, Kenji Omote, Kuniyoshi Yokoo, Kazuhiko Kawachi, Yasuhiko Kasama, Shoichi Ono, Rikizo Hatakeyama, Toshiro Kaneko, and Hiromi Tobita<\/p>\r\n<p><em>RSC Advances<\/em> <strong>2012<\/strong>, <em>2<\/em>, 10624&ndash;10631. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/ra\/c2ra21244g\" target=\"_blank\">DOI: 10.1039\/C2RA21244G<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(120) Synthesis of Tetradeca- and Pentadeca(organo)[60]fullerenes Containing Unique Photo- and Electroluminescent &pi;-Conjugated Systems<\/p>\r\n<p>Takeshi Fujita, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>Chem. Mater.<\/em> <strong>2012<\/strong>, <em>24<\/em>, 3972&ndash;3980. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cm3024296\" target=\"_blank\">DOI: 10.1021\/cm3024296<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(121) Synthesis of Thieno-Bridged Porphyrins: Changing Antiaromatic Contribution by Direction of the Thiophene Ring<\/p>\r\n<p>Yusuke Mitsushige, Shigeru Yamaguchi, Byung Sun Lee, Young Mo Sung, Susanne Kuhri, Christoph Schierl, Dirk M. Guldi, Dongho Kim, and Yutaka Matsuo<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2012<\/strong>, <em>134<\/em>, 16540&ndash;16543. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja3082999\" target=\"_blank\">DOI: 10.1021\/ja3082999<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(122) 1-Aryl-4-Silylmethyl[60]fullerenes: Synthesis, Properties, and Photovoltaic Performance<br \/>Yutaka Matsuo, Hiromi Oyama, Iwao Soga, Toshihiro Okamoto, Hideyuki Tanaka, Akinori Saeki, Shu Seki, and Eiichi Nakamura<br \/><em>Chem. Asian J.<\/em> <strong>2013<\/strong>, <em>8<\/em>, 121&ndash;128. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201200726\/abstract\" target=\"_blank\">DOI: 10.1002\/asia.201200726<\/a>]<br \/>&nbsp;<br \/>(123) Benzopyrazine-Fused Tetracene Derivatives: Thin-film Formation at the Crystalline Mesophase for Solution-Processed Hole Transporting Devices<br \/>Shungo Kojima, Toshihiro Okamoto, Kazumoto Miwa, Hiroyasu Sato, Jun Takeya, and Yutaka Matsuo<br \/><em>Org. Electron.<\/em> <strong>2013<\/strong>, <em>14<\/em>, 437&ndash;444. [<a href=\"http:\/\/dx.doi.org\/10.1016\/j.orgel.2012.10.029\" target=\"_blank\">DOI: 10.1016\/j.orgel.2012.10.029<\/a>]<\/p>\r\n<p><br \/>(124) Photostability of a Dyad of Magnesium Porphyrin and Fullerene and Its Application to Photocurrent Conversion<br \/>Takahiko Ichiki, Yutaka Matsuo, and Eiichi Nakamura<br \/><em>Chem. Commun.<\/em> <strong>2013<\/strong>, <em>49<\/em>, 279&ndash;281. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/CC\/C2CC36988E\" target=\"_blank\">DOI: 10.1039\/C2CC36988E<\/a>]<br \/>&nbsp;<br \/>(125) Small Molecule Solution-Processed Bulk Heterojunction Solar Cells with Inverted Structure Using Porphyrin Donor<br \/>Takaki Yamamoto, Junichi Hatano, Takafumi Nakagawa, Shigeru Yamaguchi, and Yutaka Matsuo<br \/><em>Appl. Phys. Lett.<\/em> <strong>2013<\/strong>, <em>102<\/em>, 013305. [<a href=\"http:\/\/dx.doi.org\/10.1063\/1.4773910\" target=\"_blank\">DOI: 10.1063\/1.4773910<\/a>]<br \/>&nbsp;<br \/>(126) Reactivity of a Metastable Cobalt(III) Trisulfide Complex: Multiple C&ndash;H Functionalization of <em>p<\/em>-Xylene and Disulfides to Afford Photofunctional Cobalt Complexes<br \/>Masashi Maruyama, Matthias K&ouml;nig, Dirk M. Guldi, Eiichi Nakamura, and Yutaka Matsuo<br \/><em>Angew. Chem. Int. Ed.<\/em> <strong>2013<\/strong>, <em>53<\/em>, 3015&ndash;3018. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201209046\/abstract\" target=\"_blank\">DOI: 10.1002\/anie.201209046<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(127) Formation of Photoconductive Nanowires of Tetracene Derivative in Composite Thin Film<br \/>Tsuyoshi Suzuki, Toshihiro Okamoto, Akinori Saeki, Shu Seki, Hiroyasu Sato, and Yutaka Matsuo<br \/><em>ACS Appl. Mater. Interfaces<\/em> <strong>2013<\/strong>, <em>5<\/em>, 1937&ndash;1942. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/am302914w\" target=\"_blank\">DOI: 10.1021\/am302914w<\/a>]<br \/>&nbsp;<br \/>(128) Magnetic Properties of Decamethyl Fullerenes: Radical Spin Interactions in Chemically Functionalized Fullerenes<br \/>Haruna Nitta, Yutaka Matsuo, Eiichi Nakamura, and Susumu Okada<br \/><em>Appl. Phys. Express<\/em> <strong>2013<\/strong>, <em>6<\/em>, 045102. [<a href=\"http:\/\/apex.jsap.jp\/link?APEX\/6\/045102\/\" target=\"_blank\">DOI: 10.7567\/APEX.6.045102<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(129) Application of Sputter-deposited Amorphous and Anatase TiO<sub>2<\/sub> as Electron-collecting Layers in Inverted Organic Photovoltaics<\/p>\r\n<p>Kee Sheng Yeo, Shoichiro Nakao, Yasushi Hirose, Tetsuya Hasegawa, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Electron.<\/em> <strong>2013<\/strong>, <em>14<\/em>, 1715&ndash;1719. [<a href=\"http:\/\/dx.doi.org\/10.1016\/j.orgel.2013.04.007\" target=\"_blank\">DOI: 10.1016\/j.orgel.2013.04.007<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(130) Regioselective [2 + 2] Cycloaddition of Fullerene Dimer with Alkyne Triggered by Thermolysis of Inter-fullerene C&ndash;C Bond<br \/>Zuo Xiao, Yutaka Matsuo, Masashi Maruyama, and Eiichi Nakamura<br \/><em>Org. Lett.<\/em> <strong>2013<\/strong>, <em>15<\/em>, 2176&ndash;2178. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol400713t\" target=\"_blank\">DOI: 10.1021\/ol400713t<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(131) Solution-Phase Synthesis of Dumbbell-Shaped C<sub>120<\/sub> by FeCl<sub>3<\/sub>-Mediated Dimerization of C<sub>60<\/sub><br \/>Masahiko Hashiguchi, Hiroshi Inada, and Yutaka Matsuo<br \/><em>Carbon<\/em> <strong>2013<\/strong>, <em>61<\/em>, 418&ndash;422. [<a href=\"http:\/\/dx.doi.org\/10.1016\/j.carbon.2013.04.101\" target=\"_blank\">DOI: 10.1016\/j.carbon.2013.04.101<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(132) First-principles Investigation on Structural and Optical Properties of M<sup>+<\/sup>@C<sub>60<\/sub> (where M = H, Li, Na, and K)<\/p>\r\n<p>Yoshifumi Noguchi, Osamu Sugino, Hiroshi Okada, and Yutaka Matsuo<\/p>\r\n<p><em>J. Phys. Chem. C<\/em> <strong>2013<\/strong>, <em>117<\/em>, 15362&ndash;15368. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jp4041259\" target=\"_blank\">DOI: 10.1021\/jp4041259<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(133) Addition of Dihydromethano Group to Fullerenes for Improving the Performance of Bulk Heterojunction Organic Solar Cells<br \/>Yutaka Matsuo, Junya Kawai, Hiroshi Inada, Takafumi Nakagawa, Hitoshi Ota, Saika Otsubo, and Eiichi Nakamura<br \/><em>Adv. Mater.<\/em> <strong>2013<\/strong>, <em>25<\/em>, 6266&ndash;6269. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adma.201302607\/abstract\" target=\"_blank\">DOI: 10.1002\/adma.201302607<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(134) Selective Synthesis of Co<sub>8<\/sub>S<sub>15<\/sub> Cluster in Bowl-shaped Template of the Pentaaryl[60]fullerene Ligand<\/p>\r\n<p>Masashi Maruyama, Kenta Imoto, Matthias K&ouml;nig, Dirk M. Guldi, Shin-ichi Ohkoshi, Eiichi Nakamura, and Yutaka Matsuo<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2013<\/strong>, <em>135<\/em>, 10914&ndash;10917. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja405045t\" target=\"_blank\">DOI: 10.1021\/ja405045t<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(135) Mixture of [60] and [70]PCBM Giving Morphological Stability in Organic Solar Cells<\/p>\r\n<p>Yoshihide Santo, Il Jeon, Kee Sheng Yeo, Takafumi Nakagawa, and Yutaka Matsuo<\/p>\r\n<p><em>Appl. Phys. Lett.<\/em> <strong>2013<\/strong>, <em>103<\/em>, 073306.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(136) Efficient Diels&ndash;Alder Addition of Cyclopentadiene to Lithium Ion Encapsulated [60]Fullerene<br \/>Hiroki Kawakami, Hiroshi Okada, and Yutaka Matsuo<br \/><em>Org. Lett.<\/em> <strong>2013<\/strong>, <em>15<\/em>, 4466&ndash;4469. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol4020046\" target=\"_blank\">DOI: 10.1021\/ol4020046<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(137) Synthesis, Photophysical Properties, and Excited State Dynamics of Platinum Complex of Tetracene Imide Disulfide<\/p>\r\n<p>Takafumi Nakagawa, Tsuyoshi Suzuki, Matthias K&ouml;nig, Dirk M. Guldi, and Yutaka Matsuo<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2013<\/strong>, <em>49<\/em>, 10394&ndash;10396. [<a href=\"http:\/\/dx.doi.org\/10.1039\/C3CC46068A\" target=\"_blank\">DOI: 10.1039\/C3CC46068A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(138) 56&pi;-Electron Hydrofullerene Derivatives as Electron Acceptors for Organic Solar Cells<\/p>\r\n<p>Yoko Abe, Rieko Hata, and Yutaka Matsuo<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2013<\/strong>, <em>42<\/em>, 1525&ndash;1527. [<a href=\"http:\/\/dx.doi.org\/10.1246\/cl.130753\" target=\"_blank\">DOI: 10.1246\/cl.130753<\/a>]&nbsp;<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(139) Low-LUMO 56&pi;-Electron Fullerene Acceptors Bearing Electron-withdrawing Cyano Groups for Small-Molecule Organic Solar Cells<\/p>\r\n<p>Yoko Abe, Takamichi Yokoyama, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Electron.<\/em> <strong>2013<\/strong>, <em>14<\/em>, 3306&ndash;3311. [DOI: <a href=\"http:\/\/dx.doi.org\/10.1016\/j.orgel.2013.09.012\" target=\"_blank\">10.1016\/j.orgel.2013.09.012<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(140) Friedel&ndash;Crafts Functionalization of the Cyclopentadienyl Ligand in Buckymetallocenes<br \/>Yutaka Matsuo, Yoichiro Kuninobu, Shingo Ito, Masaya Sawamura, and Eiichi Nakamura<br \/><em>Dalton Trans.<\/em> <strong>2014<\/strong>, <em>43<\/em>, 7407&ndash;7412. [<a href=\"http:\/\/dx.doi.org\/10.1039\/C3DT52002A\" target=\"_blank\">DOI: 10.1039\/C3DT52002A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(141) Solvent-dependent Morphology of Thermally Converted Copper Phthalocyanine for Solution-processed Small Molecule Organic Photovoltaic Devices<\/p>\r\n<p>Huihui Wang, Takamitsu Fukuda, Naoto Ishikawa, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Electron.<\/em> <strong>2014<\/strong>, <em>15<\/em>, 139&ndash;143. [<a href=\"http:\/\/dx.doi.org\/10.1016\/j.orgel.2013.10.023\" target=\"_blank\">DOI: 10.1016\/j.orgel.2013.10.023<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(142) <em>cis<\/em>-Substituted Tetraethynylporphyrin Derivatives for Small Molecule Organic Solar Cells<br \/>Yutaka Matsuo, Junichi Hatano, and Takafumi Nakagawa<br \/><em>J. Phys. Org. Chem.<\/em> <strong>2014<\/strong>, <em>27<\/em>, 87&ndash;93. [<a href=\"http:\/\/dx.doi.org\/10.1002\/poc.3241\" target=\"_blank\">DOI: 10.1002\/poc.3241<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(143) Acceleration of Tri-addition to [70]Fullerene by \"Nanom Black\" Fullerene Soot<br \/>Yutaka Matsuo, Shigeo Yasuda, Koji Suemura, and Eiichi Nakamura<br \/><em>Fullerenes, Nanotubes and Carbon Nanostructures<\/em> <strong>2014<\/strong>, <em>22<\/em>, 196&ndash;201.<br \/>[<a href=\"http:\/\/www.tandfonline.com\/doi\/full\/10.1080\/1536383X.2013.798727\" target=\"_blank\">DOI:10.1080\/1536383X.2013.798727<\/a>] (Prof. Akasaka special issue).<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(144) Anion Exchange of Li<sup>+<\/sup>@C<sub>60<\/sub> Salt for Improved Solubility<br \/>Hiroshi Okada and Yutaka Matsuo<br \/><em>Fullerenes, Nanotubes and Carbon Nanostructures<\/em> <strong>2014<\/strong>, <em>22<\/em>, 262&ndash;268.<br \/>[<a href=\"http:\/\/www.tandfonline.com\/doi\/full\/10.1080\/1536383X.2013.812639\" target=\"_blank\">DOI:10.1080\/1536383X.2013.812639<\/a>] (Prof. Akasaka special issue).<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(145) FeCl<sub>3<\/sub>-Mediated Retro-Reactions of Fullerene Derivatives to C<sub>60<\/sub><br \/>Masahiko Hashiguchi, Takao Ueno, and Yutaka Matsuo<br \/><em>Fullerenes, Nanotubes and Carbon Nanostructures<\/em>, <strong>2014<\/strong>, <em>22<\/em>, 845&ndash;852.<br \/>[DOI:10.1080\/1536383X.2012.742429]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(146) 1,8-Diazabicycloundecene-mediated Separation of Singly bonded Fullerene Dimer and Application to Facile Preparation of C<sub>61<\/sub>H<sub>2<\/sub><br \/>Yoko Abe and Yutaka Matsuo<br \/><em>Fullerenes, Nanotubes and Carbon Nanostructures<\/em>, <strong>2014<\/strong>, <em>23<\/em>, 259&ndash;262.<\/p>\r\n<p>[DOI:10.1080\/1536383X.2014.894026]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(147) Divergent Synthesis and Tuning of the Electronic Structures of Cobalt&ndash;Dithiolene&ndash;Fullerene Complexes for Organic Solar Cells<br \/>Yutaka Matsuo, Keisuke Ogumi, Masashi Maruyama, and Takafumi Nakagawa<br \/><em>Organometallics<\/em> <strong>2014<\/strong>, <em>33<\/em>, 659&ndash;664. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/om400796p\" target=\"_blank\">DOI: 10.1021\/om400796p<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(148) Direct Probing of the Structure and Electron Transfer of Fullerene\/ Ferrocene Hybrid on Au(111) Electrodes by in Situ Electrochemical STM<br \/>Ting Chen, Dong Wang, Li-Hua Gan, Yutaka Matsuo, Jing-Ying Gu, Hui-Juan Yan, Eiichi Nakamura, and Li-Jun Wan<br \/><em>J. Am. Chem. Soc.<\/em> <strong>2014<\/strong>, <em>136<\/em>, 3184&ndash;3191. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja411813r\" target=\"_blank\">DOI: 10.1021\/ja411813r<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(149) Mobility of Long-Lived Fullerene Radical in Solid State and Nonlinear Temperature Dependence<br \/>Yoko Abe, Hideyuki Tanaka, Yunlong Guo, Yutaka Matsuo, and Eiichi Nakamura<br \/><em>J. Am. Chem. Soc.<\/em> <strong>2014<\/strong>, <em>136<\/em>, 3366&ndash;3369. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja500340f\" target=\"_blank\">DOI: 10.1021\/ja500340f<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(150)&nbsp; Exciton Diffusion Length and Charge Mobility in Donor and Acceptor Materials in Organic Photovoltaics: Tetrabenzoporphyrin and Silylmethyl[60]fullerene<br \/>Hiroyuki Tamura and Yutaka Matsuo<br \/><em>Chem. Phys. Lett.<\/em> <strong>2014<\/strong>, <em>598<\/em>, 81&ndash;85. [<a href=\"http:\/\/dx.doi.org\/10.1016\/j.cplett.2014.03.013\" target=\"_blank\">DOI: 10.1016\/j.cplett.2014.03.013<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(151) Kinetic Study of the Diels&ndash;Alder Reaction of Li<sup>+<\/sup>@C<sub>60<\/sub> with Cyclohexadiene: Greatly Increased Reaction Rate by Encapsulated Li<sup>+<\/sup><\/p>\r\n<p>Hiroshi Ueno, Hiroki Kawakami, Koji Nakagawa, Hiroshi Okada, Naohiko Ikuma, Shinobu Aoyagi, Ken Kokubo, Yutaka Matsuo, and Takumi Oshima<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2014<\/strong>, <em>136<\/em>, 11162&ndash;11167. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja505952y\" target=\"_blank\">DOI: 10.1021\/ja505952y<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(152) Supramolecular Formation of Lithium-Ion-Encapsulated PCBM Fullerene with Sulfonated meso-Tetraphenylporphyrins and Long-Lived Charge Separation<\/p>\r\n<p>Yuki Kawashima, Kei Ohkubo, Hiroshi Okada, Yutaka Matsuo, and Shunichi Fukuzumi<\/p>\r\n<p><em>ChemPhysChem<\/em>, <strong>2014<\/strong>, <em>15<\/em>, 3782&ndash;3790. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/cphc.201402512\/abstract\" target=\"_blank\">DOI: 10.1002\/cphc.201402512<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(153) Influence of Additives in Bulk Heterojunction Solar Cells Using Magnesium Tetraethynylporphyrin with Triisopropylsilyl and Anthryl Substituents<\/p>\r\n<p>Takafumi Nakagawa, Junichi Hatano, and Yutaka Matsuo<\/p>\r\n<p><em>J. Porphyrins Phthalocyanines<\/em> <strong>2014<\/strong>, <em>18<\/em>, 735&ndash;740. (Prof. Nagao Kobayashi special issue [<a href=\"http:\/\/www.worldscientific.com\/doi\/abs\/10.1142\/S1088424614500655\" target=\"_blank\">DOI: 10.1142\/S1088424614500655<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(154) Electronic Infrared Light Absorption of Tri-palladium Complex Containing Two &pi;-Expanded Tetracene Ligands<\/p>\r\n<p>Tsuyoshi Suzuki, Takafumi Nakagawa, Kei Ohkubo, Shunichi Fukuzumi, and Yutaka Matsuo<\/p>\r\n<p><em>Chem. Sci.<\/em> <strong>2014<\/strong>, <em>5<\/em>, 4888&ndash;4894. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/sc\/c4sc02018a\" target=\"_blank\">DOI: 10.1039\/C4SC02018A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(155) Air-Processed Inverted Organic Solar Cells Utilizing a 2-Aminoethanol-Stabilized ZnO Nanoparticle Electron Transport Layer That Requires No Thermal Annealing<\/p>\r\n<p>Il Jeon, James W. Ryan, Tafu Nakazaki, Kee Sheng Yeo, Yuichi Negishi, and Yutaka Matsuo<\/p>\r\n<p><em>J. Mater. Chem. A<\/em> <strong>2014<\/strong>, <em>2<\/em>, 18754&ndash;18760. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2014\/TA\/c4ta04595e\" target=\"_blank\">DOI: 10.1039\/C4TA04595E<\/a>] (<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2014\/ta\/c4ta04595e\" target=\"_blank\">Inside Cover Picture<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(156) Ferromagnetic Ordering in Superatomic Solids<\/p>\r\n<p>Chul-Ho Lee, Lian Liu, Christopher Bejger, Ari Turkiewicz, Tatsuo Goko, Carlos J. Arguello, Benjamin A. Frandsen, Sky C. Cheung, Teresa Medina, Timothy J. S. Munsie, Robert D&rsquo;Ortenzio, Graeme M. Luke, Tiglet Besara, Roger A. Lalancette, Theo Siegrist, Peter W. Stephens, Andrew C. Crowther, Louis E. Brus, Yutaka Matsuo, Eiichi Nakamura, Yasutomo J. Uemura, Philip Kim, Colin Nuckolls, Michael L. Steigerwald, and Xavier Roy<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2014<\/strong>, <em>136,<\/em> 16926&ndash;16931. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja5098622\" target=\"_blank\">DOI: 10.1021\/ja5098622<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(157) Approach to High Open-circuit Voltage in Organic Solar Cells Utilizing Structural Change of Oxazolino-C<sub>70<\/sub> Derivative<\/p>\r\n<p>Shu-Hui Li, Zong-Jun Li, Takafumi Nakagawa, James W. Ryan, Yutaka Matsuo, and Xiang Gao<\/p>\r\n<p><em>Chem. Eur.<\/em> <em>J.<\/em> <strong>2015<\/strong>, <em>21<\/em>, 1894&ndash;1899. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201405890\/abstract\" target=\"_blank\">DOI: 10.1002\/chem.201405890<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(158) Multilayered MoS<sub>2<\/sub> Nanoflakes Bound to Carbon Nanotubes as Electron Acceptors in Bulk Heterojunction Inverted Organic Solar Cells<\/p>\r\n<p>Il Jeon, Dai Kutsuzawa, Yu Hashimoto, Takashi Yanase, Taro Nagahama, Toshihiro Shimada, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Electron.<\/em> <strong>2015<\/strong>, <em>17<\/em>, 275&ndash;280. [<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S1566119914005734\" target=\"_blank\">DOI: 10.1016\/j.orgel.2014.12.025<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(159) Diporphyrin Magnesium Complex with Long-Wavelength Light Absorption for Organic Solar Cells<\/p>\r\n<p>Takenari Sato, Takafumi Nakagawa, Hiroshi Okada, and Yutaka Matsuo<\/p>\r\n<p><em>J. Porphyrins Phthalocyanines<\/em> <strong>2015<\/strong>, <em>19<\/em>, 451. (Prof. Shunichi Fukuzumi special issue) [<a href=\"http:\/\/www.worldscientific.com\/doi\/abs\/10.1142\/S1088424615500303?src=recsys&amp;journalCode=jpp\" target=\"_blank\">DOI: 10.1142\/S1088424615500303<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(160) Increased Efficiency in Small Molecule Organic Solar Cells Through the Use of a 56-&pi; Electron Acceptor - Methano Indene Fullerene<\/p>\r\n<p>James W. Ryan and Yutaka Matsuo<\/p>\r\n<p><em>Sci. Rep.<\/em> <strong>2015<\/strong>, <em>5<\/em>, 8319. [<a href=\"http:\/\/www.nature.com\/srep\/2015\/150209\/srep08319\/full\/srep08319.html\" target=\"_blank\">DOI: 10.1038\/srep08319<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(161) Organic Solid Solution Composed of Two Structurally Similar Porphyrins for Organic Solar Cells<\/p>\r\n<p>Yonggang Zhen, Hideyuki Tanaka, Koji Harano, Satoshi Okada, Yutaka Matsuo, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2015<\/strong>, <em>137<\/em>, 2247&ndash;2252. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja513045a\" target=\"_blank\">DOI: 10.1021\/ja513045a<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(162) Vertical Phase Separation and Light-soaking Effect Improvements by Photoactive Layer Spin Coating Initiation Time Control in Air-processed Inverted Organic Solar Cells<\/p>\r\n<p>Il Jeon and Yutaka Matsuo<\/p>\r\n<p><em>Sol. Energy Mater. Sol. Cells<\/em> <strong>2015<\/strong>, <em>140<\/em>, 335&ndash;343. [<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0927024815001725\" target=\"_blank\">10.1016\/j.solmat.2015.04.017<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(163) A V-Shaped Polyaromatic Amphiphile: Solubilization of Various Nanocarbons in Water and Enhanced Photostability<\/p>\r\n<p>Kei Kondo, Munetaka Akita, Takafumi Nakagawa, Yutaka Matsuo, and Michito Yoshizawa<\/p>\r\n<p><em>Chem. Eur. J.<\/em> <strong>2015<\/strong>, <em>21<\/em>, 12741&ndash;12746. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201501414\/abstract\" target=\"_blank\">DOI: 10.1002\/chem.201501414<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(164) Direct and Dry Deposited Single-Walled Carbon Nanotube Films Doped with MoOx as Electron-Blocking Transparent Electrodes for Flexible Organic Solar Cells<\/p>\r\n<p>Il Jeon, Kehang Cui, Takaaki Chiba, Anton Anisimov, Albert Nasibulin, Esko Kauppinen, Shigeo Maruyama, and Yutaka Matsuo<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em> <strong>2015<\/strong>, <em>137<\/em>, 7982&ndash;7985. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.5b03739\" target=\"_blank\">DOI: 10.1021\/jacs.5b03739<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(165) Single-Walled Carbon Nanotube Film as Electrode in Indium-Free Planar Heterojunction Perovskite Solar Cells: Investigation of Electron-Blocking Layers and Dopants<\/p>\r\n<p>Il Jeon, Takaaki Chiba, Clement Delacou, Yunlong Guo, Antti Kaskela, Olivier Reynaud, Esko I. Kauppinen, Shigeo Maruyama, and Yutaka Matsuo<\/p>\r\n<p><em>Nano Lett.<\/em> <strong>2015<\/strong>, <em>15<\/em>, 6665&ndash;6671. [<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.nanolett.5b02490\" target=\"_blank\">DOI: 10.1021\/acs.nanolett.5b02490<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(166) An Enantiopure Hydrogen-Bonded Octameric Tube: Self-Sorting and Guest-Induced Rearrangement<\/p>\r\n<p>Dovil&#279; Ra&#269;kauskait&#279;, Rokas Gegevi&#269;ius, Yutaka Matsuo, Kenneth W&auml;rnmark, and Edvinas Orentas<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2015<\/strong>, <em>55<\/em>, 208&ndash;212. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201508362\/abstract\" target=\"_blank\">DOI: 10.1002\/anie.201508362<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(167) Chemical Pathways Connecting Lead(II) Iodide and Perovskite via Polymeric Plumbate(II) Fiber<\/p>\r\n<p>Yunlong Guo, Kazutaka Shoyama, Wataru Sato, Yutaka Matsuo, Kento Inoue, Koji Harano, Chao Liu, Hideyuki Tanaka, and Eiichi Nakamura<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em><strong><em><\/em><\/strong><em><\/em> <strong>2015<\/strong>, <em>137<\/em>, 15907&ndash;15914. [<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5b10599\" target=\"_blank\">DOI: 10.1021\/jacs.5b10599<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(168) Indium-free Inverted Organic Solar Cells Using Niobium-doped Titanium Oxide with Integrated Dual Function of Transparent Electrode and Electron Transport Layer<\/p>\r\n<p>Il Jeon, Shoichiro Nakao, Yasushi Hirose, Tetsuya Hasegawa, and Yutaka Matsuo<\/p>\r\n<p><em>Adv. Electron. Mater.<\/em> <strong>2016<\/strong>, <em>2<\/em>, 1500341. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/aelm.201500341\/full\" target=\"_blank\">DOI: 10.1002\/aelm.201500341<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(169) Enhancement of Open-Circuit Voltage by Using the 58-&pi; Silylmethyl Fullerenes in Small-Molecule Organic Solar Cells<\/p>\r\n<p>Il Jeon, Cl&eacute;ment Delacou, Takafumi Nakagawa, and Yutaka Matsuo<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2016<\/strong>, <em>11<\/em>, 1268&ndash;1272. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201501400\/abstract\" target=\"_blank\">DOI: 10.1002\/asia.201501400<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(170) Stability of Diketopyrrolopyrrole Small-Molecule Inverted Organic Solar Cells<\/p>\r\n<p>Il Jeon, Ryohei Sakai, Takafumi Nakagawa, Hiroki Setoguchi, and Yutaka Matsuo<\/p>\r\n<p><em>Org. Electron.<\/em> <strong>2016<\/strong>, <em>35<\/em>, 193&ndash;198. [<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S156611991630218X\" target=\"_blank\">DOI: 10.1016\/j.orgel.2016.05.022<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(171)&nbsp; Multifunctionalization of C<sub>70<\/sub> at the Two Polar Regions with a High Regioselectivity via Oxazolination and Benzylation Reactions<\/p>\r\n<p>Shu-Hui Li, Zong-Jun Li, Takafumi Nakagawa, Il Jeon, Zheng Ju, Yutaka Matsuo, and Xiang Gao<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2016<\/strong>, <em>52<\/em>, 5710&ndash;5713. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2016\/CC\/C6CC00997B\" target=\"_blank\">DOI: 10.1039\/C6CC00997B<\/a>].<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(172) Electrochemical Reduction of Cationic Li<sup>+<\/sup>@C<sub>60<\/sub> to Neutral Li<sup>+<\/sup>@C<sub>60<\/sub><sup>&bull;&ndash;<\/sup>: Isolation and Characterisation of Endohedral [60]Fulleride<\/p>\r\n<p>Hiroshi Ueno, Shinobu Aoyagi, Yu Yamazaki, Kei Ohkubo, Naohiko Ikuma, Hiroshi Okada, Tatsuhisa Kato, Yutaka Matsuo, Shunichi Fukuzumi, and Ken Kokubo<\/p>\r\n<p><em>Chem. Sci.<\/em> <strong>2016<\/strong>, <em>7<\/em>, 5770-5774. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/sc\/c6sc01209d\" target=\"_blank\">DOI: 10.1039\/C6SC01209D<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(173) Enhancement of Fill Factor in Air-processed Inverted Organic Solar Cells using Self-Assembled Monolayer of Fullerene Catechol<\/p>\r\n<p>Il Jeon, Keisuke Ogumi, Takafumi Nakagawa, and Yutaka Matsuo<\/p>\r\n<p><em>Jpn J. Appl. Phys.<\/em> <strong>2016<\/strong>, <em>55<\/em>, 082301. [<a href=\"http:\/\/iopscience.iop.org\/article\/10.7567\/JJAP.55.082301\/pdf\" target=\"_blank\">DOI: 10.7567\/JJAP.55.082301<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(174) Enhancement of Low-field Magnetoresistance in Self-Assembled Epitaxial La<sub>0.67<\/sub>Ca<sub>0.33<\/sub>MnO<sub>3<\/sub>:NiO and La<sub>0.67<\/sub>Ca<sub>0.33<\/sub>MnO<sub>3<\/sub>:Co<sub>3<\/sub>O<sub>4<\/sub> Composite Films via Polymer-Assisted Deposition<\/p>\r\n<p>Meng Zhou, Yuling Li, Il Jeon, Qinghua Yi, Xuebin Zhu, Xianwu Tang, Haiyan Wang, Ling Fei, Yuping Sun, Shuguang Deng, Yutaka Matsuo, Hongmei Luo, and Guifu Zou<\/p>\r\n<p><em>Sci. Rep.<\/em> <strong>2016<\/strong>, <em>6<\/em>, 26390. [<a href=\"http:\/\/www.nature.com\/articles\/srep26390\" target=\"_blank\">DOI:10.1038\/srep26390<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(175) Metal-electrode-free Window-like Organic Solar Cells with p-Doped Carbon Nanotube Thin-film Electrodes<\/p>\r\n<p>Il Jeon, Clement Delacou, Antti Kaskela, Esko I. Kauppinen, Shigeo Maruyama, and Yutaka Matsuo<\/p>\r\n<p><em>Sci. Rep.<\/em> <strong>2016<\/strong>, <em>6<\/em>, 31348. [<a href=\"http:\/\/www.nature.com\/articles\/srep31348\" target=\"_blank\">DOI: 10.1038\/srep31348<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(176) Interface Engineering of Metal Oxides using Ammonium Anthracene in Inverted Organic Solar Cells<\/p>\r\n<p>Il Jeon, Sasa Zeljkovic, Kei Kondo, Michito Yoshizawa, and Yutaka Matsuo<\/p>\r\n<p><em>ACS Appl. Mater. Interfaces<\/em>&nbsp;<strong>2016<\/strong>, <em>8<\/em>, 29866&ndash;29871. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acsami.6b09684\" target=\"_blank\">DOI: 10.1021\/acsami.6b09684<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(177) Regio- and Stereo-selective Intermolecular [2+2] Cycloaddition of Allenol Esters with C<sub>60<\/sub> leading to Alkylidenecyclobutane-annulated Fullerenes<br \/>Mitsuhiro Ueda, Tsukasa Sakaguchi, Miho Hayama, Takafumi Nakagawa, Yutaka Matsuo, Aiko Munechika, Shunsuke Yoshida, Hiroshi Yasuda, and Ilhyong Ryu<br \/><em>Chem. Commun.<\/em> <strong>2016<\/strong>, <em>52<\/em>, 13175-13178. [<a href=\"http:\/\/pubs.rsc.org\/is\/content\/articlelanding\/2016\/cc\/c6cc07320d\" target=\"_blank\">DOI: 10.1039\/c6cc07320d<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(178) Room Temperature-processed Inverted Organic Solar Cells using High Working-pressure-sputtered ZnO Film<br \/>Il Jeon, Yang Qian, Shoichiro Nakao, Daisuke Ogawa, Rong Xiang, Taiki Inoue, Shohei Chiashi, Tetsuya Hasegawa, Shigeo Maruyama, and Yutaka Matsuo<br \/><em>J. Mater. Chem. A<\/em> <strong>2016<\/strong>, <em>4<\/em>, 18763&ndash;18768. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/ta\/c6ta08068e\" target=\"_blank\">DOI: 10.1039\/C6TA08068E<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(179) Dual Interfacial Modifications Enable High Performance Semitransparent Perovskite Solar Cells with Large Open Circuit Voltage and Fill Factor<br \/>Qifan Xue, Yang Bai, Meiyue Liu, Ruoxi Xia, Ziming Chen, Zhicheng Hu, Xiao-Fang Jiang, Fei Huang, Shihe Yang*, Yutaka Matsuo*, Hin-Lap Yip*, and Yong Cao<br \/><em>Adv. Energy Mater.<\/em> <strong>2017<\/strong>, <em>7<\/em>, 1602333. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/aenm.201602333\/full\" target=\"_blank\">DOI: 10.1002\/aenm.201602333<\/a>] [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/aenm.201770047\/full\" target=\"_blank\">cover picture<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(180) Structures and Properties of Saturn-Like Complexes Composed of Oligothiophene Macrocycle with Methano[60]fullerene and [70]Fullerene<br \/>Masahiko Iyoda*, Hideyuki Shimizu, Shinobu Aoyagi*, Hiroshi Okada, Biao Zhou, and Yutaka Matsuo*<br \/><em>Can. J. Chem.<\/em> <strong>2017<\/strong>, <em>95<\/em>, 315&ndash;319. [<a href=\"http:\/\/www.nrcresearchpress.com\/doi\/abs\/10.1139\/cjc-2016-0461\" target=\"_blank\">DOI: 10.1139\/cjc-2016-0461<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(181) An Efficient Organic Solvent-free Solution-processing Strategy for High-mobility Metal Chalcogenide Film Growth<\/p>\r\n<p>Jie Zhao, Il Jeon, Qinghua Yi, Menka Jain, Mark H. Rummeli, Pingyuan Song, Yutaka Matsuo*, and Guifu Zou*<\/p>\r\n<p><em>Green Chem.<\/em> <strong>2017<\/strong>, <em>19<\/em>, 946&ndash;951. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/gc\/c6gc02489k\" target=\"_blank\">DOI: 10.1039\/C6GC02489K<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(182) Fullerene Cations-mediated Demethylation\/Cyclization to 5- and 7-Membered Cyclo[60]fullerene Derivatives<\/p>\r\n<p>Yutaka Matsuo*, Keisuke Ogumi, Ying Zhang, Hiroshi Okada, Takafumi Nakagawa, Hiroshi Ueno, Akiko Gocho, and Eiichi Nakamura<br \/><em>J. Mater. Chem. A<\/em> <strong>2017<\/strong>, <em>5<\/em>, 2774&ndash;2783 . [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/ta\/c6ta10319g\" target=\"_blank\">DOI: 10.1039\/C6TA10319G<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(183) Regioselective Acylation and Carboxylation of [60]Fulleroindoline via Electrochemical Synthesis<\/p>\r\n<p>Hao-Sheng Lin, Yutaka Matsuo, Jun-Jie Wang, and Guan-Wu Wang*<\/p>\r\n<p><em>Org. Chem. Front.<\/em> <strong>2017<\/strong>, <em>4<\/em>, 603&ndash;607. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2017\/QO\/C6QO00654J#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C6QO00654J<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(184) Scalable and Solid-state Redox Functionalization of Transparent Single-walled Carbon Nanotube Films for Highly Efficient and Stable Solar Cells<\/p>\r\n<p>Kehang Cui*, Yang Qian, Il Jeon, Anton Anisimov, Yutaka Matsuo, Esko I. Kauppinen, and Shigeo Maruyama*<\/p>\r\n<p><em>Adv. Energy Mater.<\/em> <strong>2017<\/strong>, <em>7<\/em>, 1700449. [<a href=\"http:\/\/dx.doi.org\/10.1002\/aenm.201700449\" target=\"_blank\">DOI: 10.1002\/aenm.201700449<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(185) Indium Tin Oxide-free Small Molecule Organic Solar Cells using Single-Walled Carbon Nanotube Electrodes<\/p>\r\n<p>Cl&eacute;ment Delacou, Il Jeon, Seungju Seo, Takafumi Nakagawa, Esko I. Kauppinen, Shigeo Maruyama, and Yutaka Matsuo*<\/p>\r\n<p><em>ECS J. Solid State Sci. Technol.<\/em> <strong>2017<\/strong>, 6, M3181&ndash;M3184. (Sir Harry Kroto memorial issue) [<a href=\"http:\/\/jss.ecsdl.org\/cgi\/content\/abstract\/6\/6\/M3181\" target=\"_blank\">DOI: 10.1149\/2.0311706jss<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(186) Crystallographic Structure Determination of Both [5,6]- and [6,6]-Isomers of Lithium-ion-containing Diphenylmethano[60]fullerene<\/p>\r\n<p>Hiroshi Okada, Hiroki Kawakami, Shinobu Aoyagi, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Org. Chem.<\/em> <strong>2017<\/strong>, <em>82<\/em>, 5868&ndash;5872. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.7b00730\" target=\"_blank\">DOI: 10.1021\/acs.joc.7b00730<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(187) Regiocontrolled Electrosynthesis of [60]Fullerene Bisadducts: Photovoltaic Performance and Crystal Structures of C<sub>60<\/sub> <em>o<\/em>\u2010Quinodimethane Bisadducts<\/p>\r\n<p>Zong-Jun Li, Sisi Wang, Shu-Hui Li, Tao Sun, Wei-Wei Yang, Kazutaka Shoyama, Takafumi Nakagawa, Il Jeon, Xiaoniu Yang, Yutaka Matsuo*, and Xiang Gao*<\/p>\r\n<p><em>J. Org. Chem.<\/em> <strong>2017<\/strong>, <em>82<\/em>, 8676&ndash;8685. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.7b01732\" target=\"_blank\">DOI: 10.1021\/acs.joc.7b01732<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(188) Highly Conductive and Transparent Large-Area Bilayer Graphene Realized by MoCl<sub>5<\/sub> Intercalation<\/p>\r\n<p>Hiroki Kinoshita, Il Jeon, Mina Maruyama, Kenji Kawahara, Yuri Terao, Dong Ding, Rika Matsumoto, Yutaka Matsuo, Susumu Okada, and Hiroki Ago*<\/p>\r\n<p><em>Adv. Mater.<\/em> <strong>2017<\/strong>, 1702141. [<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adma.201702141\/abstract\" target=\"_blank\">DOI: 10.1002\/adma.201702141<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(189) Comparative Density Functional Theory &ndash; Density Functional Tight Binding Study of Fullerene Derivatives: Effects Due to Fullerene Size, Addends, and Crystallinity on Bandstructure, Charge Transport and Optical Properties<\/p>\r\n<p>Amrita Pal, Lai Kai Wen, Chia Yao Jun, Il Jeon, Yutaka Matsuo, and Sergei Manzhos*<\/p>\r\n<p><em>Phys. Chem. Chem. Phys.<\/em> <strong>2017<\/strong>, <em>9<\/em>, 28330&ndash;28343. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/cp\/c7cp05290a#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C7CP05290A<\/a>].<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(190) Substituents Effect in Magnesium Tetraethynylporphyrin with Two Diketopyrrolopyrrole Units for Bulk Heterojunction Organic Solar Cells<\/p>\r\n<p>Keisuke Ogumi, Takafumi Nakagawa, Hiroshi Okada, Ryohei Sakai, Huan Wang, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Mater. Chem.<\/em> <em>A<\/em> <strong>2017<\/strong>, <em>5<\/em>, 23067&ndash;23077. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/ta\/c7ta07576f#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C7TA07576F<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(191) Carbon Nanotubes Versus Graphene as Flexible Transparent Electrodes in Inverted Perovskite Solar Cells<\/p>\r\n<p>Il Jeon, Jungjin Yoon, Namyoung Ahn, Mohamed Atwa, Clement Delacou, Anton Anisimov, Esko Kauppinen, Mansoo Choi*, Shigeo Maruyama*, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Phys. Chem. Lett.<\/em> <strong>2017<\/strong>, <em>8<\/em>, 5395&ndash;5401. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.jpclett.7b02229\" target=\"_blank\">DOI: 10.1021\/acs.jpclett.7b02229<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(192) Synthesis and Crystal Structure of Li<sup>+<\/sup>@Fluoreno[60]fullerene: Effect of Encapsulated Lithium Ion on Electrochemistry of Spiroannelated Fullerene<\/p>\r\n<p>Hiroshi Ueno, Hiroshi Okada, Shinobu Aoyagi, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Org. Chem.<\/em> <strong>2017<\/strong>, <em>82<\/em>, 11631&ndash;11635. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.joc.7b01893\" target=\"_blank\">DOI: 10.1021\/acs.joc.7b01893<\/a>].<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(193) Perovskite Solar Cells Using Carbon Nanotubes Both as Cathode and as Anode<\/p>\r\n<p>Il Jeon, Seungju Seo, Yuta Sato, Clement Delacou, Anton Anisimov, Kazutomo Suenaga, Esko Kauppinen*, Shigeo Maruyama*, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Phys. Chem. C<\/em> <strong>2017<\/strong>, <em>121<\/em>, 25743&ndash;25749. [<a href=\"http:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.jpcc.7b10334\" target=\"_blank\">DOI: 10.1021\/acs.jpcc.7b10334<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(194) A Fluorenylidene-Acridane That Becomes Dark in Color upon Grinding &ndash; Ground State Mechanochromism by Conformational Change<\/p>\r\n<p>Tsuyoshi Suzuki, Hiroshi Okada, Takafumi Nakagawa, Kazuki Komatsu, Chikako Fujimoto, Hiroyuki Kagi, and Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Sci.<\/em> <strong>2018<\/strong>, <em>9<\/em>, 475&ndash;482. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2018\/SC\/C7SC03567E#!divAbstract\" target=\"_blank\">DOI: 10.1039\/c7sc03567e<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(195) Carbon-Sandwiched Perovskite Solar Cell<\/p>\r\n<p>Namyoung Ahn, Il Jeon, Jungjin Yoon, Esko I. Kauppinen, Yutaka Matsuo*, Shigeo Maruyama*, and Mansoo Choi*<\/p>\r\n<p><em>J. Mater. Chem. A<\/em> <strong>2018<\/strong>, <em>6<\/em>, 1382&ndash;1389. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2018\/TA\/C7TA09174E#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C7TA09174E<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(196) A Helically-Twisted Ladder Based on 9,90-Bifluorenylidene: Synthesis, Characterization, and Charge Transport Properties<\/p>\r\n<p>Jinjia Xu, Atsuro Takai*, Alisa Bannaron, Takafumi Nakagawa, Yutaka Matsuo, Manabu Sugimoto, Yoshitaka Matsushita and Masayuki Takeuchi*<\/p>\r\n<p><em>Mater. Chem. Front.<\/em> <strong>2018<\/strong>, <em>2<\/em>, 780&ndash;784. [<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2018\/QM\/C7QM00583K#!divAbstract\" target=\"_blank\">DOI: 10.1039\/c7qm00583k<\/a>]&nbsp;<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(197) Lithium-Ion Endohedral Fullerene (Li<sup>+<\/sup>@C<sub>60<\/sub>) Dopant in Stable Perovskite Solar Cells Inducing Anti-Oxidation<\/p>\r\n<p>Il Jeon, Hiroshi Ueno, Seungju Seo, Kerttu Aitola, Ryosuke Nishikubo, Akinori Saeki, Hiroshi Okada, Gerrit Boschloo, Shigeo Maruyama, and Yutaka Matsuo*<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2018<\/strong>, <em>57<\/em>, 4607&ndash;4611. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201800816\" target=\"_blank\">DOI: 10.1002\/anie.201800816<\/a>]&nbsp;<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(198) Engineering High-performance and Air-stable PBTZT-stat-BDTT-8:PC<sub>61<\/sub>BM\/PC<sub>71<\/sub>BM Organic Solar Cells<\/p>\r\n<p>Il Jeon, Ryohei Sakai, Seungju Seo, Graham E. Morse, Hiroshi Ueno, Takafumi Nakagawa, Yang Qian, Shigeo Maruyama, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Mater. Chem. A<\/em> <strong>2018<\/strong>, <em>6<\/em>, 5746&ndash;5751. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/ta\/c7ta11095b#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C7TA11095B<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(199)&nbsp;Anthracene-based Organic Small-molecule Electron-injecting Material for Inverted Organic Light-emitting Diodes<\/p>\r\n<p>Yutaka Matsuo*, Hiroshi Okada, Yasuhiro Kondo, Il Jeon, Huan Wang, Yun Yu, Takeshi Matsushita, Motoki Yanai, and Toshiaki Ikuta<\/p>\r\n<p><em>ACS Appl. Mater. Interfaces<\/em> <strong>2018<\/strong>, <em>10<\/em>, 11810&ndash;11817. [<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acsami.8b00603\" target=\"_blank\">DOI: 10.1021\/acsami.8b00603<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(200) Fullerene-Cation-Mediated Noble-Metal-Free Direct Introduction of Functionalized Aryl Groups onto [60]Fullerene<\/p>\r\n<p>Xiao-Yu Yang, Hao-Sheng Lin, Il Jeon, and Yutaka Matsuo*<\/p>\r\n<p><em>Org. Lett.<\/em> <strong>2018<\/strong>, <em>20<\/em>, 3372&ndash;3376. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.8b01295\" target=\"_blank\">DOI: 10.1021\/acs.orglett.8b01295<\/a>]<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<p>(201) Electronic Structure and Cohesive Energy of Silyl-methyl-fullerene and Methano-indene-fullerene Solids<\/p>\r\n<p>Sho Furutani, Yutaka Matsuo, Susumu Okada*<\/p>\r\n<p><em>Jpn. J. Appl. Phys.<\/em> <strong>2018<\/strong>, 57, 085102. [<a href=\"http:\/\/iopscience.iop.org\/article\/10.7567\/JJAP.57.085102\" target=\"_blank\">DOI: 10.7567\/JJAP.57.085102<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(202) Structure of [60]Fullerene with Mobile Lithium Cation Inside<\/p>\r\n<p>Shinobu Aoyagi*, Kazuhira Miwa, Hiroshi Ueno, Hiroshi Okada, Yutaka Matsuo, Ken Kokubo<\/p>\r\n<p><em>Royal Soc. Open Sci.<\/em> <strong>2018<\/strong>, <em>5<\/em>, 180337. [<a href=\"http:\/\/dx.doi.org\/10.1098\/rsos.180337\" target=\"_blank\">DOI: 10.1098\/rsos.180337<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(203) Polymeric Acid-doped Transparent Carbon Nanotube Electrodes in Organic Solar Cells with the Longest Doping Durability<\/p>\r\n<p>Il Jeon, Clement Delacou, Hiroshi Okada, Graham E. Morse, Tae-Hee Han, Yuta Sato, Anton Anisimov, Kazu Suenaga, Esko I. Kauppinen, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>J. Mater. Chem. A<\/em> <strong>2018<\/strong>, <em>6<\/em>, 14553&ndash;14559. [<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/ta\/c8ta03383h#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C8TA03383H<\/a>]<\/p>\r\n<p>(Selected as <a href=\"http:\/\/pubs.rsc.org\/en\/journals\/articlecollectionlhttp:\/\/pubs.rsc.org\/en\/journals\/articlecollectionlanding?sercode=ta&amp;themeid=f7d0c2cb-4131-4611-8a14-f0c78308057d\" target=\"_blank\">2018 <em>Journal of Materials Chemistry A<\/em> HOT Papers<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(204) Non-doped and Unsorted Single-walled Carbon Nanotubes as Carrier-selective, Transparent, and Conductive Electrode for Perovskite Solar Cells<\/p>\r\n<p>Takahiro Sakaguchi, Il Jeon, Takaaki Chiba, Ahmed Shawky, Rong Xiang, Shohei Chiashi, Esko I. Kauppinen, Nam-Gyu Park*, Yutaka Matsuo*, Shigeo Maruyama*<\/p>\r\n<p><em>MRS Commun.<\/em> <strong>2018<\/strong>, <em>8<\/em>, 1058&ndash;1063. [<a href=\"https:\/\/doi.org\/10.1557\/mrc.2018.142\" target=\"_blank\">DOI: 10.1557\/mrc.2018.142<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(205) Enhanced Electrical Conduction in Anatase TaON via Soft Chemical Lithium Insertion towards Electronics Application<\/p>\r\n<p>Atsushi Suzuki, Yasushi Hirose*, Takafumi Nakagawa, Satoshi Fujiwara, Shoichiro Nakao, Yutaka Matsuo, Isao Harayama, Daiichiro Sekiba, Tetsuya Hasegawa*<\/p>\r\n<p><em>ACS Appl. Nano Mater.<\/em> <strong>2018<\/strong>, <em>1<\/em>, 3981&ndash;3985. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsanm.8b00750\" target=\"_blank\">DOI: 10.1021\/acsanm.8b00750<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(206) Magnesium Tetra(phenylethynyl)porphyrin: Stepwise Synthetic Route, Crystal Structures, and Longer Singlet Excited State Lifetime than Zinc Congener<\/p>\r\n<p>Takafumi Nakagawa, Huan Wang, Anna Zieleniewska, Hiroshi Okada, Shinobu Aoyagi, Dirk M. Guldi, Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Asian J.<\/em> <strong>2018<\/strong>, <em>13<\/em>, 3032&ndash;3039. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/asia.201800994\" target=\"_blank\">DOI: 10.1002\/asia.201800994<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(207) Octaalkoxyfullerenes: Widely LUMO-Tunable <em>C<\/em><sub>2<em>v<\/em><\/sub>-Symmetric Fullerene Derivatives<\/p>\r\n<p>Hiroshi Ueno*, Kouya Uchiyama, Yue Ma, Keita Watanabe, Kenji Yoza, Yutaka Matsuo*, Hiroshi Moriyama*<\/p>\r\n<p><em>J. Org. Chem.<\/em> <strong>2018<\/strong>, <em>83<\/em>, 10655&ndash;10659. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.8b01485\" target=\"_blank\">DOI: 10.1021\/acs.joc.8b01485<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(208) Achieving High Efficiency in Solution-Processed Perovskite Solar Cells using C<sub>60<\/sub>\/C<sub>70<\/sub> Mixed Fullerenes<\/p>\r\n<p>Hao-Sheng Lin, Il Jeon*, Rong Xiang, Seungju Seo, Jin-Wook Lee, Chao Li, Amrita Pal, Sergei Manzhos, Mark Goorsky, Yang Yang, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>ACS Appl. Mater. Interfaces<\/em> <strong>2018<\/strong>, <em>10<\/em>, 39590&ndash;39598. [<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acsami.8b11049\" target=\"_blank\">DOI: 10.1021\/acsami.8b11049<\/a>] (<a href=\"https:\/\/pubs.acs.org\/toc\/aamick\/10\/46\" target=\"_blank\">Selected as a Cover Picture<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(209) Vapor-Assisted <em>Ex-Situ<\/em> Doping of Carbon Nanotube towards Efficient and Stable Perovskite Solar Cells<\/p>\r\n<p>Jin-Wook Lee, Il Jeon, Hao-Sheng Lin, Seungju Seo, Tae-Hee Han, Anton Anisimov, Esko I. Kauppinen, Yutaka Matsuo*, Shigeo Maruyama*, Yang Yang*<\/p>\r\n<p><em>Nano Lett.<\/em> <strong>2019<\/strong>, <em>19<\/em>, 2223&ndash;2230. [<a href=\"https:\/\/pubs.acs.org.ccindex.cn\/doi\/10.1021\/acs.nanolett.8b04190\" target=\"_blank\">DOI: 10.1021\/acs.nanolett.8b04190<\/a>] (<a href=\"https:\/\/pubs.acs.org\/toc\/nalefd\/19\/4\" target=\"_blank\">Selected as a Cover Art<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(210) Polarity Engineering of Porous Aromatic Frameworks for Specific Water Contaminants Capture<br \/>Xiaoshan Shen, Muhammad Faheem, Yutaka Matsuo, Saba Aziz, Xu Zhang, Yuhan Li, Jian Song , Yuyang Tian*, Guangshan Zhu<br \/><em>J. Mater. Chem. A<\/em> <strong>2019<\/strong>, <em>7<\/em>, 2507&ndash;2512. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/ta\/c8ta11343b\" target=\"_blank\">DOI: 10.1039\/C8TA11343B<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(211) Fluorescein-based Fluorescent Porous Aromatic Framework for Fe<sup>3+<\/sup> Detection with High Sensitivity<br \/>Tingting Ma, Xue Zhao, Yutaka Matsuo, Jian Song, Rui Zhao, Muhammad Faheem, Mo Chen, Yunfeng Zhang, Yuyang Tian*, Guangshan Zhu<br \/><em>J. Mater. Chem. C<\/em> <strong>2019<\/strong>, <em>7<\/em>, 2327&ndash;2332. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/tc\/c8tc06288a\" target=\"_blank\">DOI: 10.1039\/C8TC06288A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(212) Formation of Environmentally Stable Hole-doped Graphene Films: Instantaneous and High-density Carrier Doping by a Boron-Based Oxidant<\/p>\r\n<p>Kaito Kanahashi, Naoki Tanaka, Yoshiaki Shoji, Mina Maruyama, Il Jeon, Kenji Kawahara, Masatou Ishihara, Masataka Hasegawa, Hiromichi Ohta, Hiroki Ago, Yutaka Matsuo, Susumu Okada, Takanori Fukushima, Taishi Takenobu*<\/p>\r\n<p><em>npj 2D Materials and Applications<\/em>&nbsp;<strong>2019<\/strong>, <em>3<\/em>, 7. [<a href=\"https:\/\/www.nature.com\/articles\/s41699-019-0090-x\" target=\"_blank\">DOI: 10.1038\/s41699-019-0090-x<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(213) Reduced Knoevenagel Reaction of Acetetracenylene-1,2-dione with Acceptor Units for Luminescent Tetracene Derivatives<\/p>\r\n<p>Yutaka Matsuo*, Chu-Guo Yu, Takafumi Nakagawa, Hiroshi Okada, Hiroshi Ueno, Tian-Ge Sun, Yu-Wu Zhong<\/p>\r\n<p><em>J. Org. Chem.<\/em> <strong>2019<\/strong>, <em>84<\/em>, 2339&ndash;2345. [<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.joc.8b03083\" target=\"_blank\">DOI: 10.1021\/acs.joc.8b03083<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(214) Star-shaped Magnesium Tetraethynylporphyrin Bearing Four Peripheral Electron-accepting Diketopyrrolopyrrole Functionalities for Organic Solar Cells<\/p>\r\n<p>Huan Wang, Qihui Yue, Takafumi Nakagawa, Anna Zieleniewska, Hiroshi Okada, Keisuke Ogumi, Hiroshi Ueno, Dirk M. Guldi*, Xiaozhang Zhu*, Yutaka Matsuo*<\/p>\r\n<p><em>J. Mater. Chem. A<\/em> <strong>2019<\/strong>, <em>7<\/em>, 4072&ndash;4083. [<a href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2019\/TA\/C8TA10710F\" target=\"_blank\">DOI: 10.1039\/c8ta10710f<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(215) Highly Soluble <em>C<\/em><sub>2<em>v<\/em><\/sub> -symmetrical Fullerene Derivatives: Efficient Synthesis, Characterization, and Electrochemical Study<\/p>\r\n<p>Yue Ma, Kouya Uchiyama, Hiroshi Ueno*, Hiroshi Okada, Hiroshi Moriyama*, Yutaka Matsuo*<\/p>\r\n<p><em>Org. Chem. Front.<\/em> <strong>2019<\/strong>, <em>6<\/em>, 1372&ndash;1377. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/qo\/c9qo00056a\" target=\"_blank\">DOI: 10.1039\/c9qo00056a<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(216) Effects of Optical Interference and Optimized Crystallinity in Organic Photovoltaic Cells with a Low-bandgap Small Molecule Fabricated by Dry Process<\/p>\r\n<p>Kohei Yamamoto*, Tetsuhiko Miyadera, Yutaka Matsuo, Takayuki Kuwabara, Kohshin Takahashi, Tetsuya Taima, Masayuki Chikamatsu<\/p>\r\n<p><em>Jpn. J. Appl. Phys.<\/em> <strong>2019<\/strong>, <em>58<\/em>, SBBG12. [<a href=\"https:\/\/doi.org\/10.7567\/1347-4065\/aafe6b\" target=\"_blank\">DOI: 10.7567\/1347-4065\/aafe6b<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(217) High-Working-Pressure Sputtering of ZnO for Stable and Efficient Perovskite Solar Cells<\/p>\r\n<p>Abhishek Thote, Il Jeon*, Hao-Sheng Lin, Sergei Manzhos, Takafumi Nakagawa, Donguk Suh, Junho Hwang, Makoto Kashiwagi, Junichiro Shiomi, Shigeo Maruyama*, Hirofumi Daiguji*, Yutaka Matsuo*<\/p>\r\n<p><em>ACS Appl. Electron. Mater.<\/em> <strong>2019<\/strong>, <em>1<\/em>, 389&ndash;396. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsaelm.8b00105\" target=\"_blank\">DOI: 10.1021\/acsaelm.8b00105<\/a>] (<a href=\"https:\/\/pubs.acs.org\/toc\/aaembp\/1\/3\" target=\"_blank\">Selected as a Cover Art<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(218) Stable and Reproducible 2D\/3D Formamidinium&ndash;Lead&ndash;Iodide Perovskite Solar Cells<\/p>\r\n<p>Abhishek Thote, Il Jeon*, Jin-Wook Lee, Seungju Seo, Hao-Sheng Lin, Yang Yang, Hirofumi Daiguji*, Shigeo Maruyama*, Yutaka Matsuo*<\/p>\r\n<p><em>ACS Appl. Energy Mater.<\/em> <strong>2019<\/strong>, <em>2<\/em>, 2486&ndash;2493. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsaem.8b01964\" target=\"_blank\">DOI : 10.1021\/acsaem.8b01964<\/a>] (<a href=\"https:\/\/pubs.acs.org\/toc\/aaemcq\/2\/4\" target=\"_blank\">Selected as a Cover Art<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(219) Mechanochromism, Twisted\/Folded Structure Determination, and Derivatization of (<em>N<\/em>\u2010Phenylfluorenylidene)acridane<\/p>\r\n<p>Yutaka Matsuo*, Ya Wang, Hiroshi Ueno, Takafumi Nakagawa, Hiroshi Okada<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2019<\/strong>,&nbsp;<em>58<\/em>, 8762&ndash;8767. [<a href=\"https:\/\/doi.org\/10.1002\/anie.201902636\" target=\"_blank\">DOI: 10.1002\/anie.201902636<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(220) Synthesis of Benzothieno[60]fullerenes Through Fullerenyl Cation Intermediates<\/p>\r\n<p>Yutaka Matsuo*, Yun Yu, Xiao-Yu Yang, Hiroshi Ueno, Hiroshi Okada, Hiromasa Shibuya, Yeong Suk Choi, Yong Wan Jin<\/p>\r\n<p><em>J. Org. Chem.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>84<\/em>, 6270&ndash;6277. [<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.9b00549\" target=\"_blank\">DOI: 10.1021\/acs.joc.9b00549<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(221) Improved Solubility of Asymmetric Tetraethynylporphyrin Derivatives for Solution-processed Organic Solar Cells<\/p>\r\n<p>Keisuke Ogumi, Takafumi Nakagawa, Hiroshi Okada, Yutaka Matsuo*<\/p>\r\n<p><em>Org. Electron.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>71<\/em>, 50&ndash;57. [<a href=\"https:\/\/doi.org\/10.1016\/j.orgel.2019.04.036\" target=\"_blank\">DOI: 10.1016\/j.orgel.2019.04.036<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(222) Semiconducting Carbon Nanotubes as Crystal Growth Templates and Grain Bridges in Perovskite Solar Cells<\/p>\r\n<p>Seungju Seo, Il Jeon*, Rong Xiang, Changsoo Lee, Hao Zhang, Takeshi Tanaka, Jin-Wook Lee, Donguk Suh, Tatsuro Ogamoto, Ryosuke Nishikubo, Akinori Saeki, Shohei Chiashi, Junichiro Shiomi, Hiromichi Kataura, Hyuck Mo Lee, Yang Yang, Yutaka Matsuo*, Shigeo Maruyama*<\/p>\r\n<p><em>J. Mater. Chem. A<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>7<\/em>, 12987&ndash;12992. [<a href=\"https:\/\/doi.org\/10.1039\/C9TA02629K%20\" target=\"_blank\">DOI: 10.1039\/C9TA02629K<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(223) High-Performance Solution-Processed Double-Walled Carbon Nanotube Transparent Electrode for Perovskite Solar Cells<\/p>\r\n<p>Il Jeon, Jungjin Yoon, Unsoo Kim, Changsoo Lee, Rong Xiang, Ahmed Shawky, Jun Xi, Junseop Byeon, Hyuck Mo Lee, Mansoo Choi*, Shigeo Maruyama*, Yutaka Matsuo*<\/p>\r\n<p><em>Adv. Energy Mater.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>9<\/em>, 1901204. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/aenm.201901204\" target=\"_blank\">DOI: 10.1002\/aenm.201901204<\/a>] (<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/aenm.201970105\" target=\"_blank\">Selected as a Cover Art<\/a>)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(224) Chemical Reduction of Li<sup>+<\/sup>@C<sub>60<\/sub>&nbsp;by Decamethylferrocene to Produce Neutral Li<sup>+<\/sup>@C<sub>60<\/sub><sup>&bull;&ndash;<\/sup><\/p>\r\n<p>Hiroshi Okada, Hiroshi Ueno, Yasuhiro Takabayashi, Takeshi Nakagawa, Martina Vranki&#263;, John Arvanitidis, Tetsuro Kusamoto, Kosmas Prassides*, Yutaka Matsuo*<\/p>\r\n<p><em>Carbon<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>153<\/em>, 467&ndash;471. [<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0008622319307158\" target=\"_blank\">DOI: 10.1016\/j.carbon.2019.07.028<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(225) Dialkoxymethano[60]fullerenes as Electron Acceptors in Thin-film Organic Solar Cell&nbsp;<\/p>\r\n<p>Mohammed Y. Suleiman, Yue Ma, Takafumi Nakagawa, Hiroshi Ueno, Yutaka Matsuo*<\/p>\r\n<p><em>Tetrahedron<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>75<\/em>, 130514. [<a href=\"https:\/\/doi.org\/10.1016\/j.tet.2019.130514\" target=\"_blank\">DOI:&nbsp;10.1016\/j.tet.2019.130514<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(226) Synergic Catalysts of Polyoxometalate@Cationic Porous Aromatic Framework: Reciprocal Modulation of Both Capture and Conversion Materials<\/p>\r\n<p>Jian Song, Yue Li, Ping Cao, Xiaofei Jing, Muhammad Faheem, Yutaka Matsuo, Youliang Zhu, Yuyang Tian*, Xiaohong Wang, Guangshan Zhu*<\/p>\r\n<p><em>Adv. Mater.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>31<\/em>, 1902444. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/adma.201902444\" target=\"_blank\">DOI: 10.1002\/adma.201902444<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(227) Li@C<sub>60<\/sub>&nbsp;Endohedral Fullerene as Supraatomic Dopant for C<sub>60<\/sub>&nbsp;Electron-transporting Layer Promoting Efficiency of Perovskite Solar Cells<\/p>\r\n<p>Hiroshi Ueno, Il Jeon, Hao-sheng Lin, Abhishek Thote, Takafumi Nakagawa, Hiroshi Okada, Seiichiro Izawa, Masahiro Hiramoto, Hirofumi Daiguji, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Commun.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>55<\/em>, 11837&ndash;11839. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/CC\/C9CC06120G\" target=\"_blank\">DOI: 10.1039\/c9cc06120g<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(228) Investigation of Charge Interaction between Fullerene Derivatives and Single-Walled Carbon Nanotubes<\/p>\r\n<p>Cl&eacute;ment Delacou, Il Jeon*, Keigo Otsuka, Taiki Inoue, Anton Anisimov, Takenori Fujii, Esko I. Kauppinen, Shigeo Maruyama*, Yutaka Matsuo*<\/p>\r\n<p><em>InfoMat<\/em>&nbsp;<strong>2019<\/strong>, <em>1<\/em>, 559&ndash;570. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/inf2.12045\" target=\"_blank\">DOI: 10.1002\/inf2.12045<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(229) Highly Selective and Scalable Fullerene-Cation-Mediated Synthesis accessing Cyclo[60]fullerenes with 5-Membered-Carbon-Ring and their Application to Perovskite Solar Cells<\/p>\r\n<p>Hao-Sheng Lin, Il Jeon*, Yingqian Chen, Xiao-Yu Yang, Takafumi Nakagawa, Shigeo Maruyama, Sergei Manzhos, Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Mater.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>31<\/em>, 8432&ndash;8439. [<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.chemmater.9b02468\" target=\"_blank\">DOI: 10.1021\/acs.chemmater.9b02468<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(230) Controlled Redox of Lithium-ion Endohedral Fullerene for Efficient and Stable Metal Electrode-Free Perovskite Solar Cells<\/p>\r\n<p>Il Jeon*, Ahmed Shawky, Hao-Sheng Lin, Seungju Seo, Hiroshi Okada, Jin-Wook Lee, Amrita Pal, Shaun Tan, Anton Anisimov, Esko I. Kauppinen, Yang Yang, Sergei Manzhos, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>141<\/em>, 16553&ndash;16558. [<a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/jacs.9b06418\" target=\"_blank\">DOI: 10.1021\/jacs.9b06418<\/a>]<\/p>\r\n<p>&nbsp;&nbsp;<\/p>\r\n<p>(231) High-yielding Pd<sub>2<\/sub>(dba)<sub>3<\/sub>&middot;C<sub>6<\/sub>H<sub>6<\/sub>-based Four-fold Sonogashira Coupling with Selenophene-conjugated Magnesium Tetraethynylporphyrin for Organic Solar Cells<\/p>\r\n<p>Huan Wang, Takafumi Nakagawa, Meng-Meng Zhang, Keisuke Ogumi, Shangfeng Yang*, Yutaka Matsuo*<\/p>\r\n<p><em>RSC Adv.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>9<\/em>, 32562&ndash;32572. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/ra\/c9ra07393k\" target=\"_blank\">DOI: 10.1039\/C9RA07393K<\/a>]<\/p>\r\n<p>&nbsp;&nbsp;<\/p>\r\n<p>(232) Prediction of Magnesium Tetraethynylporphyrin&rsquo;s Solubility by Theoretical Calculation<\/p>\r\n<p>Keisuke Ogumi, Yutaka Matsuo*<\/p>\r\n<p><em>J. Porphyrins Phthalocyanines<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>23<\/em>, 1144&ndash;1148. [<a href=\"https:\/\/doi.org\/10.1142\/S1088424619501475\" target=\"_blank\">DOI: 10.1142\/S1088424619501475<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(233) Highly Selective Synthesis of Tetrahydronaphthaleno[60]fullerenes via Fullerene-Cation-Mediated Intramolecular Cyclization<\/p>\r\n<p>Xiao-Yu Yang, Hao-Sheng Lin, Yutaka Matsuo*<\/p>\r\n<p><em>J. Org. Chem.<\/em>&nbsp;<strong>2019<\/strong>, <em>84<\/em>, 16314&ndash;16322. [<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.9b02618\" target=\"_blank\">DOI: 10.1021\/acs.joc.9b02618<\/a>]<\/p>\r\n<p>&nbsp;&nbsp;<\/p>\r\n<p>(234) Multifunctional Effect of p-Doping, Anti-Reflection, and Encapsulation by Polymeric Acid for High Efficiency and Stable Carbon Nanotube-based Silicon Solar Cells<\/p>\r\n<p>Yang Qian, Il Jeon*, Ya-Lun Ho, Changhyun Lee, Sujeong Jeong, Clement Delacou, Anton Anisimov, Esko I. Kaupinnen, Yutaka Matsuo, Yoonmook Kang, Hae-Seok Lee, Donghwan Kim, Jean-Jacques Delaunay, Shigeo Maruyama*<\/p>\r\n<p><em>Adv. Energy Mater.&nbsp;<\/em><strong>2020<\/strong>, <em>10<\/em>, 1902389. [<a href=\"https:\/\/doi.org\/10.1002\/aenm.201902389\" target=\"_blank\">DOI: 10.1002\/aenm.201902389<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(235) Nickel-Catalyzed Deaminative Acylation of Activated Aliphatic Amines with Aromatic Amides via C&ndash;N Bond Activation<\/p>\r\n<p>Chu-guo Yu, Yutaka Matsuo*<\/p>\r\n<p><em>Org. Lett.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>22<\/em>, 950&ndash;955. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b04497\" target=\"_blank\">DOI: 10.1021\/acs.orglett.9b04497<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(236) Polyaromatic Nanotweezers on Semiconducting Carbon Nanotubes for the Growth and Interfacing of Lead Halide Perovskite Crystal Grains in Solar Cells<\/p>\r\n<p>Hao-Sheng Lin, Shunhei Okawa, Yue Ma, Satoshi Yotsumoto, Changsoo Lee, Shaun Tan, Sergei Manzhos, Michito Yoshizawa, Shohei Chiashi, Hyuck Mo Lee, Takeshi Tanaka, Hiromichi Kataura, Il Jeon*, Yutaka Matsuo*, Shigeo Maruyama*<\/p>\r\n<p><em>Chem. Mater.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>32<\/em>, 5125&ndash;5133. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.chemmater.0c01011\" target=\"_blank\">DOI: 10.1021\/acs.chemmater.0c01011<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(237) Carbon Nanotubes to Outperform Metal Electrodes in Perovskite Solar Cells via Dopant Engineering and Hole-Selectivity Enhancement<\/p>\r\n<p>Il Jeon*, Ahmed Shawky, Seungju Seo, Yang Qian, Anton Anisimov, Esko I. Kauppinen, Yutaka Matsuo*, Shigeo Maruyama*<\/p>\r\n<p><em>J. Mater. Chem. A<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>8<\/em>, 11141&ndash;11147. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/ta\/d0ta03692g\" target=\"_blank\">DOI: 10.1039\/D0TA03692G<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(238) MoS<sub>2<\/sub>-Carbon Nanotube Heterostructure as Efficient Hole Transporters and Conductors in Perovskite Solar Cells<\/p>\r\n<p>Yang Qian, Seungju Seo, Il Jeon*, Haosheng Lin, Shuhei Okawa, Yongjia Zheng, Ahmed Shawky, Anton Anisimov, Esko I. Kauppinen, Jing Kong, Rong Xiang, Yutaka Matsuo, Shigeo Maruyama*<\/p>\r\n<p><em>Appl. Phys. Express<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>13<\/em>, 075009. [<a href=\"https:\/\/iopscience.iop.org\/article\/10.35848\/1882-0786\/ab9efa\" target=\"_blank\">DOI: 10.35848\/1882-0786\/ab9efa<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(239) Denatured M13 Bacteriophage-Templated Perovskite Solar Cells Exhibiting High Efficiency<\/p>\r\n<p>Hao\u2010Sheng Lin, Jong\u2010Min Lee, Jiye Han, Changsoo Lee, Seungju Seo, Shaun Tan, Hyuck Mo Lee, Eun Jung Choi, Michael S. Strano, Yang Yang, Shigeo Maruyama, Il Jeon, Yutaka Matsuo, Jin\u2010Woo Oh<\/p>\r\n<p><em>Adv. Sci.<\/em>&nbsp;<strong>2020<\/strong>, <em>7<\/em>, 2000782. [<a href=\"https:\/\/doi.org\/10.1002\/advs.202000782\" target=\"_blank\">DOI: 10.1002\/advs.202000782<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(240) Equilibrium and Thermodynamic Studies of Chromic Overcrowded Fluorenylidene-Acridanes with Modified Fluorene Moieties<\/p>\r\n<p>Ya Wang, Yue Ma, Keisuke Ogumi, Bing Wang, Takafumi Nakagawa, Yao Fu, Yutaka Matsuo*<\/p>\r\n<p><em>Comm. Chem.<\/em>&nbsp;<strong>2020<\/strong>, <em>3<\/em>, 93. [<a href=\"https:\/\/doi.org\/10.1038\/s42004-020-00345-6\" target=\"_blank\">DOI: 10.1038\/s42004-020-00345-6<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(241) Solvation-Free Li<sup>+<\/sup>&nbsp;Lewis Acid Enhancing Reaction: Kinetic Study of [5,6]-Li<sup>+<\/sup>@PCBM to [6,6]-Li<sup>+<\/sup>@PCBM<\/p>\r\n<p>Yue Ma, Hiroshi Ueno, Hiroshi Okada, Sergei Manzhos*, Yutaka Matsuo*<\/p>\r\n<p><em>Org. Lett.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>22<\/em>, 18, 7239&ndash;7243. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c02570\" target=\"_blank\">DOI: 10.1021\/acs.orglett.0c02570<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(242) Magnesium Diethynylporphyrin Derivatives with Strong Near-Infrared Absorption for Solution-process Bulk Heterojunction Organic Solar Cells<\/p>\r\n<p>Keisuke Ogumi, Takafumi Nakagawa, Masahiro Nakano, and Yutaka Matsuo*<\/p>\r\n<p><em>J. Porphyrins Phthalocyanines<\/em>&nbsp;<strong>2021<\/strong>, 25, 128&ndash;134. [<a href=\"https:\/\/doi.org\/10.1142\/S1088424621500036\">DOI: 10.1142\/S1088424621500036<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(243) Controlled Removal of Surfactants from Double\u2010Walled Carbon Nanotubes for Stronger p\u2010Doping Effect and Its Demonstration in Perovskite Solar Cells<\/p>\r\n<p>Ahmed Shawky, Jeong\u2010Seok Nam, Kyusun Kim, Jiye Han, Jungjin Yoon, Seungju Seo, Chang Soo Lee, Rong Xiang, Yutaka Matsuo, Hyuck Mo Lee, Shigeo Maruyama*, Il Jeon*<\/p>\r\n<p><em>Small Method<\/em> <strong>2021<\/strong>, <em>5<\/em>, 210080. [<a href=\"https:\/\/doi.org\/10.1002\/smtd.202100080\" target=\"_blank\">DOI: 10.1002\/smtd.202100080<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(244) Synthesis of 5,15-meso-Bis(2-chlorothiophen-3-yl)porphyrin as a Building Block for Further Functional Materials Safi Ullah, Safi Ullah, Keisuke Ogumi, Xuelin Zheng, Huan Wang, Yutaka Matsuo*<\/p>\r\n<p><em>J. Porphyrins Phthalocyanines<\/em> <strong>2021<\/strong>, <em>25<\/em>, 944&ndash;950. [<a href=\"https:\/\/www.worldscientific.com\/doi\/abs\/10.1142\/S1088424621500590\" target=\"_blank\">DOI: 10.1142\/S1088424621500590<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(245) Cationic Nitrogen-doped Graphene as p-Type Modifier for High-performance PEDOT:PSS Hole-transporters in Organic Solar Cells<\/p>\r\n<p>Hao-Sheng Lin, Takuhei Kaneko, Soma Ishikawa, Il Jeon, Sangwoo Chae, Takumi Yana, Nagahiro Saito, Yutaka Matsuo*<\/p>\r\n<p><em>Jpn. J. Appl. Phys.<\/em> <strong>2021<\/strong>, <em>60<\/em>, 070902. [<a href=\"https:\/\/doi.org\/10.35848\/1347-4065\/ac00fc\" target=\"_blank\">DOI: 10.35848\/1347-4065\/ac00fc<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(246) One-step Direct Oxidation of Alkoxy to Ketone for Evaporable Fullerene-fused Ketone as Efficient Electron-transport Materials<\/p>\r\n<p>Hao-Sheng Lin, Yue Ma, Rong Xiang, Sergei Manzhos, Il Jeon, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>Communications Chemistry<\/em> <strong>2021<\/strong>, <em>4<\/em>, 74. [<a href=\"https:\/\/doi.org\/10.1038\/s42004-021-00511-4\" target=\"_blank\">DOI: 10.1038\/s42004-021-00511-4<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(247) Multi-Walled Carbon Nanotube-Assisted Encapsulation Approach for Stable Perovskite Solar Cells<\/p>\r\n<p>Jin-Myung Choi, Hiroki Suko, Kyusun Kim, Jiye Han, Sangsu Lee, Yutaka Matsuo, Shigeo Maruyama, Il Jeon*, Hirofumi Daiguji*<\/p>\r\n<p><em>Molecules<\/em>&nbsp;<strong>2021<\/strong>, 26, 5060. [<a href=\"https:\/\/www.mdpi.com\/1420-3049\/26\/16\/5060\" target=\"_blank\">DOI: 10.3390\/molecules26165060<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(248) An Adamantane Capsule and Efficient Uptake of Spherical Guests upto 3 nm in Water<\/p>\r\n<p>Yuri Katagiri, Yamato Tsuchida, Yutaka Matsuo, Michito Yoshizawa*<\/p>\r\n<p><em>J. Am. Chem. Soc. <\/em><strong>2021<\/strong>,&nbsp;<em>143<\/em>, 21492&ndash;21496.&nbsp;[<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.1c11021\" target=\"_blank\">DOI: 10.1021\/jacs.1c11021<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(249) Synthesis of Conjugated Donor-Acceptor Antiaromatic Porphyrin and Their Application to Perovskite Solar Cells<\/p>\r\n<p>Xue-Lin Zheng, Hao-Sheng Lin, Bo-Wen Zhang, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>J. Org. Chem.<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>87<\/em>, 5457&ndash;5463. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.1c01947\" target=\"_blank\">DOI: 10.1021\/acs.joc.1c01947<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(250) Facile Multiple Alkylations of C60 Fullerene<\/p>\r\n<p>Kazuhira Miwa, Shinobu Aoyagi*, Takahiro Sasamori*, Shogo Morisako, Hiroshi Ueno, Yutaka Matsuo, Hideki Yorimitsu<\/p>\r\n<p><em>Molecules<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>27<\/em>, 450. [<a href=\"https:\/\/www.mdpi.com\/1420-3049\/27\/2\/450\" target=\"_blank\">DOI: 10.3390\/molecules27020450<\/a>]&nbsp;<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(251) Scalable eDIPS-based Single-walled Carbon Nanotube Films for Conductive Transparent Electrodes in Organic Solar Cells<\/p>\r\n<p>Hao-Sheng Lin, Riku Hatomoto, Daisuke Miyata, Miftakhul Huda, Il Jeon, Satoru Hashimoto, Takeshi Hashimoto, Yutaka Matsuo*<\/p>\r\n<p><em>Applied Physics Express<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>15<\/em>, 046505. [DOI\uff1a<a href=\"https:\/\/iopscience.iop.org\/article\/10.35848\/1882-0786\/ac5c02\">10.35848\/1882-0786\/ac5c02<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(252) Multi-Functional MoO3 Doping of Carbon-Nanotube Top Electrodes for Highly Transparent and Efficient Semi-Transparent Perovskite Solar Cells<\/p>\r\n<p>Seungju Seo, Kosuke Akino, Jeong-Seok Nam, Ahmed Shawky, Hao-Sheng Lin, Hiroki Nagaya, Esko I. Kauppinen, Rong Xiang, Yutaka Matsuo, Il Jeon*, Shigeo Maruyama*<\/p>\r\n<p><em>Advanced Materials Interfaces<\/em>&nbsp;<strong>2022<\/strong>, 9, 2101595. [DOI :&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/admi.202101595\">10.1002\/admi.202101595<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(253) Triarylamine\/Bithiophene Copolymer with Enhanced Quinoidal Character as Hole-Transporting Material for Perovskite Solar Cells<\/p>\r\n<p>Hao-Sheng Lin, Takahiro Doba, Wataru Sato, Yutaka Matsuo*, Rui Shang*, Eiichi Nakamura*<\/p>\r\n<p><em>Angew. Chem. Int. Ed.<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>61<\/em>, e202203949. [<a href=\"https:\/\/doi.org\/10.1002\/anie.202203949\" target=\"_blank\">DOI: 10.1002\/anie.202203949<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(254) Quantitative and High-resolution Mechanical Pressure Sensing Functions of Mechanochromic Fluorenylidene-acridane<\/p>\r\n<p>Keisuke Ogumi, Kohki Nagata, Yuki Takimoto, Kentaro Mishiba, Yutaka Matsuo*<\/p>\r\n<p><em>J. Mater. Chem. C<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>10<\/em>, 11181&ndash;11186. [<a href=\"https:\/\/doi.org\/10.1039\/D2TC01988D\" target=\"_blank\">DOI: 10.1039\/D2TC01988D<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(255) Synthesis of n-Type [60]Fullerene Derivatives with Sterically Bulky&nbsp;<em>tert<\/em>-Butyl Groups for Vacuum Deposition Processes<\/p>\r\n<p>Hiromasa Shibuya, Yeong Suk Choi*, Taejin Choi, Sungyoung Yun, Juhee Moon, Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Asian J.<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>17<\/em>, e202200609. [<a href=\"https:\/\/doi.org\/10.1002\/asia.202200609\" target=\"_blank\">DOI: 10.1002\/asia.202200609<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(256) Synthesis of Neutral Li-endohedral PCBM: An n-Dopant for Fullerene Derivatives<\/p>\r\n<p>Hiroshi Ueno*, Daiki Kitabatake, Hao-Sheng Lin, Yue Ma, Il Jeon, Seiichiro Izawa, Masahiro Hiramoto, Fuminori Misaizu, Shigeo Maruyama, Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Commun.<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>58<\/em>, 10190&ndash;10193. [<a href=\"https:\/\/doi.org\/10.1039\/D2CC03678A\" target=\"_blank\">DOI: 10.1039\/D2CC03678A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(257) Inkjet Printing of Mechanochromic Fluorenylidene-Acridane<\/p>\r\n<p>Keisuke Ogumi, Kohki Nagata, Yuki Takimoto, Kentaro Mishiba, Yutaka Matsuo<\/p>\r\n<p><em>Sci. Rep.<\/em>&nbsp;<strong>2022<\/strong>, in press.<\/p>\r\n<p>&nbsp;<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>Accounts and Reviews<\/h4>\r\n<p>(1) Creation of Cyclic &pi;-Electron Conjugated Systems through the Functionalization of Fullerenes and Synthesis of Their Multinuclear Metal Complexes<\/p>\r\n<p>Yutaka Matsuo*<\/p>\r\n<p><em>Bull. Chem. Soc. Jpn.<\/em> <strong>2008<\/strong>, <em>81<\/em>, 320&ndash;330. (Award Accounts). [<a href=\"http:\/\/www.jstage.jst.go.jp\/article\/bcsj\/81\/3\/81_320\/\" target=\"_blank\">DOI: 10.1246\/bcsj.81.320<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) Selective Multi-addition of Organocopper Reagents to Fullerenes<\/p>\r\n<p>Yutaka Matsuo and Eiichi Nakamura*<\/p>\r\n<p><em>Chem. Rev.<\/em> <strong>2008<\/strong>, <em>108<\/em>, 3016&ndash;3028. [<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/cr0684218\" target=\"_blank\">DOI: 10.1021\/cr0684218<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) Design Concept for High-LUMO-Level Fullerene Electron-acceptors for Organic Solar Cells<\/p>\r\n<p>Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Lett.<\/em> <strong>2012<\/strong>, <em>41<\/em>, 754&ndash;759. (Highlight Review) [<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/cl\/41\/8\/41_CL-120682\/_article\" target=\"_blank\">DOI: 10.1246\/cl.2012.754<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) The Chemistry of Four-Membered Aromatics<\/p>\r\n<p>Yutaka Matsuo* and Masashi Maruyama<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2012<\/strong>, <em>48<\/em>, 9334&ndash;9342. (Feature Article) [<a href=\"http:\/\/xlink.rsc.org\/?doi=C2CC34244H\" target=\"_blank\">DOI: 10.1039\/C2CC34244H<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(5) Polymer-Fullerene Solar Cells<\/p>\r\n<p>Il Jeon and Yutaka Matsuo*<\/p>\r\n<p><em>Encyclopedia of Polymer Science and Technology<\/em> <strong>2017<\/strong>, 1&ndash;17.<\/p>\r\n<p>[<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/0471440264.pst650\/abstract\" target=\"_blank\">DOI: 10.1002\/0471440264.pst650<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(6) Single-walled Carbon Nanotubes in Solar Cells<\/p>\r\n<p>Il Jeon, Yutaka Matsuo, and Shigeo Maruyama*<\/p>\r\n<p><em>Top. Curr. Chem.<\/em> <strong>2018<\/strong>, <em>376<\/em>, 4. [<a href=\"https:\/\/link.springer.com\/article\/10.1007%2Fs41061-017-0181-0\" target=\"_blank\">DOI: 10.1007\/s41061-017-0181-0<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(7) Functionalization of [60]Fullerene through Fullerene Cation Intermediates<\/p>\r\n<p>Hao-Sheng Lin and Yutaka Matsuo*<\/p>\r\n<p><em>Chem. Commun.<\/em> <strong>2018<\/strong>, <em>54<\/em>, 11244&ndash;11259. (Feature Article) [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/cc\/c8cc05965a#!divAbstract\" target=\"_blank\">DOI: 10.1039\/C8CC05965A<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(8) Single-Walled Carbon Nanotubes in Emerging Solar Cells: Synthesis and Electrode Applications<\/p>\r\n<p>Il Jeon, Rong Xiang, Ahmed Shawky, Yutaka Matsuo, Shigeo Maruyama*<\/p>\r\n<p><em>Adv. Energy Mater.<\/em> <strong>2019<\/strong>, <em>9<\/em>, 1801312. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/aenm.201801312\" target=\"_blank\">DOI: 10.1002\/aenm.201801312<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(9) Recent Progress in Porphyrin- and Phthalocyanine-containing Perovskite Solar Cells<\/p>\r\n<p>Yutaka Matsuo*, Keisuke Ogumi, Il Jeon, Huan Wang, and Takafumi Nakagawa<\/p>\r\n<p><em>RSC Adv<\/em>. <strong>2020<\/strong>, <em>10<\/em>, 32678&ndash;32689. [<a href=\"https:\/\/doi.org\/10.1039\/d0ra03234d\">DOI: 10.1039\/d0ra03234d<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(10) Creation of Highly Efficient and Durable Organic and Perovskite Solar Cells Using Nanocarbon Materials<\/p>\r\n<p>Yutaka Matsuo*<\/p>\r\n<p><em>Bull. Chem. Soc. Jpn.<\/em> <strong>2021<\/strong>, <em>94<\/em>, 1080&ndash;1089. [<a href=\"https:\/\/doi.org\/10.1246\/bcsj.20200404\" target=\"_blank\">DOI: 10.1246\/bcsj.20200404<\/a>] (Prof. Eiichi Nakamura special issue)<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>Books<\/h4>\r\n<p>(1) Endohedral Lithium-containing Fullerenes: Preparation, Derivatization, and Application<\/p>\r\n<p>Yutaka Matsuo*, Hiroshi Okada, Hiroshi Ueno<\/p>\r\n<p>Springer, <strong><\/strong>Singapore, 2017. [DOI 10.1007\/978-981-10-5004-6] [ISBN: 978-981-10-5003-9] [<a href=\"https:\/\/link.springer.com\/book\/10.1007\/978-981-10-5004-6\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>Chapters in Books<\/h4>\r\n<p>(1) Polymerization of Methyl Methacrylate Initiated by Half-Metallocene Complexes of Tantalum: Ligand Architecture Leading to Living Polymerization, Kazushi Mashima, Yutaka Matsuo, and Kazuhide Tani<\/p>\r\n<p>in \"Future Technology for Polyolefin and Olefin Polymerization Catalysis\" Edited by M. Terano and T. Shiono,<\/p>\r\n<p>Technology and Education Publishers, Tokyo, 2002, p98-103.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) Unique Complexation and Catalytic Performance of Zirconium and Hafnium Complexes Bearing N-Aryliminomethylpyrrolyl Ligand, Yutaka Matsuo, Hayato Tsurugi, Takahiro Yasumoto, and Kazushi Mashima<\/p>\r\n<p>in \"Current Achievements on Heterogeneous Olefin Polymerization Catalysts\" Edited by M. Terano,<\/p>\r\n<p>Sankeisya Co. Ltd., Nagoya, 2004, p151-157.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) Cyclophenacene Cut Out of Fullerene, Yutaka Matsuo and Eiichi Nakamura<\/p>\r\n<p>in \"Functional Organic Materials: Syntheses, Strategies and Applications\" Edited by Thomas J. J. M&uuml;ller and Uwe H. F. Bunz<\/p>\r\n<p>Wiley-VCH, Weinheim, 2007, p59-80 (Chapter 2). [<a href=\"http:\/\/as.wiley.com\/WileyCDA\/WileyTitle\/productCd-3527313028.html\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) Application of Fullerenes to Nanodevices, Yutaka Matsuo and Eiichi Nakamura<\/p>\r\n<p>in \"Chemistry of Nanocarbons\" Edited by F. Wudl, S. Nagase and T. Akasaka<\/p>\r\n<p>Wiley-Blackwell, 2010, p173-187 (Chapter 6). [<a href=\"http:\/\/as.wiley.com\/WileyCDA\/WileyTitle\/productCd-0470721952.html\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(5) Solution-processable Small Molecule Organic Photovoltaic Devices, Yutaka Matsuo<br \/>in \"Trends in Advanced Sensitized and Organic Solar Cells\" (ISBN: 978-4-7813-0620-9) Edited by T. Miyasaka<br \/>CMC Publishing Co., Ltd., 2012, p222&ndash;231. [<a href=\"http:\/\/www.cmcbooks.co.jp\/products\/detail.php?product_id=4315\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(6) Molecular Assembly and Organization of Fullerenes for Photoelectric Conversion, Yutaka Matsuo<\/p>\r\n<p>\"Metal&ndash;Molecular Assembly for Functional Materials\" (ISBN 978-4-431-54369-5) Edited by Y. Matsuo et al.<\/p>\r\n<p>Springer, Berlin, Germany, 2013 (Chapter 1). [<a href=\"http:\/\/www.springer.com\/chemistry\/inorganic+chemistry\/book\/978-4-431-54369-5\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(7) Fullerene Derivatives as Electron Acceptors in Polymer Solar Cells, Yutaka Matsuo<\/p>\r\n<p>\"Polymer Photovoltaics: Materials, Physics, and Device Engineering\" Edited by F. Huang, H.-L. Yip, and Y. Cao<\/p>\r\n<p>RSC Publishing, Cambridge, UK, 2015 (Chapter 4). [<a href=\"http:\/\/www.rsc.org\/images\/Polymer_Photovoltaics_tcm18-244492.pdf\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(8) Fullerene Derivatives for Organic Solar Cells, Yutaka Matsuo<\/p>\r\n<p>\"Chemical Science of &pi;-Electron Systems\" Edited by T. Akasaka, A. Osuka, S. Fukuzumi, H. Kandori, Y. Aso<\/p>\r\n<p>Springer, Berlin, Germany, 2015 (Chapter 36). [<a href=\"http:\/\/www.springer.com\/us\/book\/9784431553564\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(9) Fullerenes in Photovoltaics, in \"Handbook of Fullerene Science and Technology\" Hao-Sheng Lin, Yutaka Matsuo [<a href=\"https:\/\/doi.org\/10.1007\/978-981-13-3242-5_37-1\" target=\"_blank\">DOI: 10.1007\/978-981-13-3242-5_37-1<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(10) Lithium Endohedral Fullerenes, in \"Handbook of Fullerene Science and Technology\" Yue Ma, Yutaka Matsuo [<a href=\"https:\/\/doi.org\/10.1007\/978-981-13-3242-5_31-1\" target=\"_blank\">DOI: 10.1007\/978-981-13-3242-5_31-1<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(11) Recent Progress in Porphyrin Derivatives Used in Organic Thin-film Solar Cells, in \"Applications of Porphyrinoids as Functional Materials\" Yutaka Matsuo, Keisuke Ogumi [<a href=\"https:\/\/doi.org\/10.1039\/9781839164149-00204\" target=\"_blank\">DOI: 10.1039\/9781839164149-00204<\/a>]<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>\u66f8\u7c4d\uff08\u8457\u66f8\uff0c\u76e3\u4fee\uff09<\/h4>\r\n<p>(1) \u300c\u91d1\u5c5e\u3068\u5206\u5b50\u96c6\u5408\u30fc\u6700\u65b0\u6280\u8853\u3068\u5fdc\u7528\u30fc\u300d\uff08\u76e3\u4fee\uff09\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248<\/p>\r\n<p>2010\u5e7411\u6708\uff08ISBN: 978-4781302928\uff09[<a href=\"http:\/\/www.cmcbooks.co.jp\/books\/r0501.php\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) \u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u79d1\u5b66\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u5316\u5b66\u540c\u4eba<\/p>\r\n<p>2011\u5e744\u6708\uff08ISBN 978-4-7598-1298-5\uff09[<a href=\"http:\/\/www.kagakudojin.co.jp\/book\/b86726.html\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) \u300c\u6709\u6a5f\u534a\u5c0e\u4f53\u306b\u304a\u3051\u308b\u5404\u7a2e\u7269\u6027\u306e\u6e2c\u5b9a\u4e8b\u4f8b\u3068\u8a55\u4fa1\u65b9\u6cd5\u300d\uff08\u96fb\u5b50\u66f8\u7c4d\uff09\uff0c\u60c5\u5831\u6a5f\u69cb<\/p>\r\n<p>2011\u5e7412\u6708\uff08ISBN 978-4-905545-22-4\uff09<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) \u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u6700\u524d\u7dda\u300d\uff08\u76e3\u4fee\uff09\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248<\/p>\r\n<p>2012\u5e747\u6708\uff08ISBN 978-4-7813-0600-1\uff09[<a href=\"http:\/\/www.cmcbooks.co.jp\/products\/detail.php?product_id=4137\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(5) \u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\u300d\uff08\u76e3\u4fee\uff09\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248<\/p>\r\n<p>2014\u5e744\u6708\uff08ISBN 978-4-7813-0937-8\uff09[<a href=\"http:\/\/www.cmcbooks.co.jp\/products\/detail.php?product_id=4636\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>\u66f8\u7c4d\uff08\u30c1\u30e3\u30d7\u30bf\u30fc\u57f7\u7b46\uff09<\/h4>\r\n<p>(1) \u6709\u6a5f\u91d1\u5c5e\u53cd\u5fdc\u5264\u30cf\u30f3\u30c9\u30d6\u30c3\u30af\uff08\u7389\u5c3e\u6667\u5e73\u7de8\uff09\uff0c\u5316\u5b66\u540c\u4eba\uff0c2003\u5e74<\/p>\r\n<p>\u300c\u30ea\u30c1\u30a6\u30e0\u300d\uff0c\u4e2d\u6751\u6804\u4e00\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 24&ndash;29.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) \u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u7528\u30ab\u30fc\u30dc\u30f3\u6280\u8853\u5927\u5168\u96c6\uff0c\u6280\u8853\u60c5\u5831\u5354\u4f1a\uff0c2004\u5e74<\/p>\r\n<p>&nbsp;\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u8868\u9762\u4fee\u98fe\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4e2d\u6751\u6804\u4e00\uff0cpp. 151&ndash;162.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) \u30ca\u30ce\u30ab\u30fc\u30dc\u30f3\u30cf\u30f3\u30c9\u30d6\u30c3\u30af\uff0c\u30a8\u30cc\u30fb\u30c6\u30a3\u30fc\u30fb\u30a8\u30b9\uff0c2007\u5e74<\/p>\r\n<p>\u300c\u7fbd\u6839\u4ed8\u304d\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u5408\u6210\u3068\u6a5f\u80fd\u304a\u3088\u3073\u30d5\u30e9\u30fc\u30ec\u30f3\uff0f\u30d5\u30a7\u30ed\u30bb\u30f3\u30cf\u30a4\u30d6\u30ea\u30c3\u30c9\u306e\u5408\u6210\u3068\u96fb\u5b50\u30fb\u5149\u96fb\u5b50\u6a5f\u80fd\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4e2d\u6751\u6804\u4e00\uff0cpp. 627&ndash;632.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) \u8d85\u5206\u5b50\u30b5\u30a4\u30a8\u30f3\u30b9\uff06\u30c6\u30af\u30ce\u30ed\u30b8\u30fc\uff0c\u30a8\u30cc\u30fb\u30c6\u30a3\u30fc\u30fb\u30a8\u30b9\uff0c2009\u5e74<\/p>\r\n<p>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u30cf\u30a4\u30d6\u30ea\u30c3\u30c9\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 477&ndash;485.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(5) \u6709\u6a5f\u30c7\u30d0\u30a4\u30b9\u306e\u305f\u3081\u306e\u5857\u5e03\u6280\u8853\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2012\u5e74<\/p>\r\n<p>\u300c\u4f4e\u5206\u5b50\u5857\u5e03\u578b\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 220&ndash;229.<br \/><br \/>(6) \u30ca\u30ce\u30ab\u30fc\u30dc\u30f3 \u70ad\u7d20\u6750\u6599\u306e\u57fa\u790e\u3068\u5fdc\u7528\uff0c\u8fd1\u4ee3\u79d1\u5b66\u793e\uff0c2012\u5e74<br \/>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u300d\uff08\u7b2c\uff12\u7ae0\uff09\uff0c\u5927\u6fa4\u6620\u4e8c\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 19&ndash;61.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(7) \u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2012\u5e74<\/p>\r\n<p>\u300c\u9ad8LUMO\u30d5\u30e9\u30fc\u30ec\u30f3\u8a2d\u8a08\u306e\u30b3\u30f3\u30bb\u30d7\u30c8\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 66&ndash;77.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(8) \u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2012\u5e74<\/p>\r\n<p>\u300c\u9577\u6ce2\u9577\u9818\u57df\u306e\u5149\u5438\u53ce\u3092\u793a\u3059\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u6750\u6599\u300d\uff0c\u9234\u6728\u3000\u6bc5\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 42&ndash;52.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(9) \u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2012\u5e74<\/p>\r\n<p>\u300c\u975e\u30d5\u30e9\u30fc\u30ec\u30f3\u30a2\u30af\u30bb\u30d7\u30bf\u30fc\u6750\u6599\u300d\uff0c\u6ce2\u591a\u91ce\u6df3\u4e00\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 100&ndash;112.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(10) \u9ad8\u6b21&pi;\u7a7a\u9593\u306e\u5275\u767a\u3068\u6a5f\u80fd\u958b\u767a\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2013\u5e74<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306b\u7528\u3044\u308b\u9ad8\u6a5f\u80fd\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u8a2d\u8a08\u3068\u5408\u6210\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 178&ndash;182.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(11) CSJ\u30ab\u30ec\u30f3\u30c8\u30ec\u30d3\u30e5\u30fc \u672a\u6765\u6750\u6599\u3092\u5275\u51fa\u3059\u308b&pi;\u96fb\u5b50\u7cfb\u306e\u79d1\u5b66\uff0c\u5316\u5b66\u540c\u4eba\uff0c2013\u5e74<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e&pi;\u96fb\u5b50\u79d1\u5b66\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 138&ndash;145.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(12) \u96fb\u6c17\u5316\u5b66\/\u30a4\u30f3\u30d4\u30fc\u30c0\u30f3\u30b9\u6e2c\u5b9a\u306e\u30ce\u30a6\u30cf\u30a6\u3068\u6b63\u3057\u3044\u30c7\u30fc\u30bf\u89e3\u91c8\uff0c\u6280\u8853\u60c5\u5831\u5354\u4f1a\uff0c2013\u5e74<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u30ad\u30e3\u30ea\u30a2\u79fb\u52d5\u5ea6\u6e2c\u5b9a\u300d\uff0c\u4e2d\u5ddd\u8cb4\u6587\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 455&ndash;458.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(13) \u4eba\u5de5\u5149\u5408\u6210\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2013\u5e74<\/p>\r\n<p>\u300c\u9769\u65b0\u7684\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 221&ndash;228.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(14) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74<\/p>\r\n<p>\u300c\u4ee3\u8868\u7684\u306a\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 19&ndash;30.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(15) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74<\/p>\r\n<p>\u300c\u5869\u5316\u7b2c\u4e8c\u9244\u3092\u7528\u3044\u308b\u30d5\u30e9\u30fc\u30ec\u30f3\u4fee\u98fe\u53cd\u5fdc\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp.31&ndash;39<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(16) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74<\/p>\r\n<p>\u300c\u30ea\u30c1\u30a6\u30e0\u30a4\u30aa\u30f3\u5185\u5305\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u5408\u6210\u3068\u7cbe\u88fd\u300d\uff0c\u5ca1\u7530\u6d0b\u53f2\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u6cb3\u5730\u548c\u5f66\uff0c\u7b20\u9593\u6cf0\u5f66\uff0cpp. 103&ndash;109<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(17) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74<\/p>\r\n<p>\u300c\u30ea\u30c1\u30a6\u30e0\u30a4\u30aa\u30f3\u5185\u5305\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u6709\u6a5f\u5316\u5b66\u4fee\u98fe\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u5ca1\u7530\u6d0b\u53f2\uff0cpp. 110&ndash;116.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(18) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306b\u7528\u3044\u308b\u30e1\u30bf\u30ce\u30a4\u30f3\u30c7\u30f3\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u69cb\u9020\u3068\u5149\u96fb\u5909\u63db\u7279\u6027\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 163&ndash;169.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(19) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30fb\u5185\u5305\u6280\u8853\u306e\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74<\/p>\r\n<p>\u300c\u4f4e\u3044LUMO\u6e96\u4f4d\u3092\u3082\u3064\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u300d\uff0c\u5b89\u90e8\u967d\u5b50\uff0c\u677e\u5c3e\u3000\u8c4a\uff0cpp. 170&ndash;177.<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(20) \u30ca\u30ce\u7c92\u5b50\u306e\u8868\u9762\u4fee\u98fe\u3068\u5206\u6790\u8a55\u4fa1\u6280\u8853\uff0c\u60c5\u5831\u6a5f\u69cb\uff0c2016\u5e74<\/p>\r\n<p>\u300c\u70ad\u7d20\u6750\u6599\u30fb\u30ca\u30ce\u30ab\u30fc\u30dc\u30f3\u306e\u8868\u9762\u4fee\u98fe\u3068\u305d\u306e\u8a55\u4fa1\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(21) \u30ab\u30fc\u30dc\u30f3\u30ca\u30ce\u30c1\u30e5\u30fc\u30d6\u30fb\u30b0\u30e9\u30d5\u30a7\u30f3\u306e\u5fdc\u7528\u7814\u7a76\u6700\u524d\u7dda\uff0cNTS\uff0c2016\u5e74<\/p>\r\n<p>\u300cCNT\u8584\u819c\u3092\u900f\u660e\u96fb\u6975\u3068\u3057\u3066\u7528\u3044\u305f\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u958b\u767a\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(22) \u30da\u30ed\u30d6\u30b9\u30ab\u30a4\u30c8\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u958b\u767a\u6700\u524d\u7dda\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2019\u5e74<\/p>\r\n<p>\u300c\u30ab\u30fc\u30dc\u30f3\u30ca\u30ce\u30c1\u30e5\u30fc\u30d6\u819c\u3092\u7528\u3044\u305f\u9769\u65b0\u7684\u30da\u30ed\u30d6\u30b9\u30ab\u30a4\u30c8\u578b\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4e38\u5c71\u8302\u592b<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>\u7dcf\u8aac\uff08\u65e5\u672c\u8a9e\uff09<\/h4>\r\n<p>(1) \u65e5\u672c\u7d50\u6676\u5b66\u4f1a\u8a8c\u30002006\u5e74, vol.48, pp. 277&ndash;282.<\/p>\r\n<p>\u300c\u74b0\u72b6&pi;\u96fb\u5b50\u5171\u5f79\u7cfb\u30fb\u30b7\u30af\u30ed\u30d5\u30a7\u30ca\u30bb\u30f3\u306e\u5408\u6210\u3068\u69cb\u9020\u7814\u7a76\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4e2d\u6751\u6804\u4e00<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c\u30002007\u5e74, vol.65, pp. 44&ndash;53.<\/p>\r\n<p>\u300c\u5b98\u80fd\u57fa\u5316\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u5408\u6210\u3068\u69cb\u9020\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4e2d\u6751\u6804\u4e00<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) \u932f\u4f53\u5316\u5b66\u4f1a\u8a8c\u30002010\u5e74, vol.55, pp. 39&ndash;51 (Award Accounts).<\/p>\r\n<p>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u91d1\u5c5e\u932f\u4f53\u306e\u5408\u6210\u3068\u6a5f\u80fd\u306e\u7814\u7a76\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c\uff0c2012\u5e74, vol.70, pp. 541&ndash;548.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306b\u7528\u3044\u3089\u308c\u308b\u9ad8\u3044LUMO\u6e96\u4f4d\u3092\u3082\u3064\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>\u89e3\u8aac\u8a18\u4e8b<\/h4>\r\n<p>(1) \u672a\u6765\u6750\u6599\uff0cNTS\uff0c2003\u5e74, 4\u6708\u53f7, p6-12.<\/p>\r\n<p>\u300c\u6709\u6a5f\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u5f62\u4f5c\u308b\u8d85\u5206\u5b50\u69cb\u9020\u3000-\u819c\u3068\u6db2\u6676-\u300d\uff0c\u4e2d\u6751\u6804\u4e00\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u78ef\u90e8\u5bdb\u4e4b\uff0c\u6fa4\u6751\u6b63\u4e5f<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(2) Organometallic News\uff0c\u8fd1\u757f\u5316\u5b66\u5354\u4f1a\uff0c2003, 121, 151.<\/p>\r\n<p>\u300c\u65b0\u3057\u3044\u7a2e\u985e\u306e\u30ab\u30fc\u30dc\u30f3\u30ea\u30c3\u30c1\u6709\u6a5f\u91d1\u5c5e\u5316\u5408\u7269\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(3) \u30d5\u30a1\u30eb\u30de\u30b7\u30a2\uff0c\u65e5\u672c\u85ac\u5b66\u4f1a\uff0c2004\u5e74, vol. 40, No. 11, p1007-1011.<\/p>\r\n<p>\u300c\u6a5f\u80fd\u6027\u6709\u6a5f\u30d5\u30e9\u30fc\u30ec\u30f3\u3092\u7528\u3044\u305f\u751f\u547d\u79d1\u5b66\u304a\u3088\u3073\u6750\u6599\u79d1\u5b66\u3078\u306e\u5c55\u958b\u300d\uff0c\u4e2d\u6751\u6804\u4e00\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u78ef\u90e8\u5bdb\u4e4b<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(4) New Diamond\u3000\u7b2c80\u53f7\uff0c\u30cb\u30e5\u30fc\u30c0\u30a4\u30e4\u30e2\u30f3\u30c9\u30d5\u30a9\u30fc\u30e9\u30e0\uff0c2006\u5e74, vol.22, p21.<\/p>\r\n<p>\u300c\u5316\u5b66\u4fee\u98fe\u30d5\u30e9\u30fc\u30ec\u30f3\u306b\u79d8\u3081\u3089\u308c\u305f\u7121\u9650\u306e\u53ef\u80fd\u6027\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(5) \u5316\u5b66\uff0c\u5316\u5b66\u540c\u4eba\uff0c2006\u5e74, vol. 61, No. 12, p58-59.<\/p>\r\n<p>\u300c\u5149\u96fb\u5909\u63db\u30c7\u30d0\u30a4\u30b9\u4e2d\u306b\u304a\u3051\u308b\u5206\u5b50\u96c6\u5408\u4f53\u69cb\u9020\u306e\u5f71\u97ff\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(6) \u932f\u4f53\u5316\u5b66\u4f1a\u8a8c\uff0c\u932f\u4f53\u5316\u5b66\u4f1a\uff0c2007\u5e74, vol. 50, p86-87.<\/p>\r\n<p>\u300cGordon Research Conference 2007 (Organometallic Chemistry) \u5831\u544a\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(7) Organometallic News\uff0c\u8fd1\u757f\u5316\u5b66\u5354\u4f1a\uff0c2008\u5e74, No. 1, p38.<\/p>\r\n<p>\u300c\u7570\u7a2e\u4e8c\u6838\u91d1\u5c5e\u932f\u4f53\u30dd\u30ea\u30de\u30fc\u3092\u7528\u3044\u305f\u5408\u91d1\u30ca\u30ce\u7c92\u5b50\u306e\u5408\u6210\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(8) \u5316\u5b66\uff0c\u5316\u5b66\u540c\u4eba\uff0c2008\u5e74, vol. 63, No. 11, p30-35.<\/p>\r\n<p>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u9077\u79fb\u91d1\u5c5e\u932f\u4f53\u306e\u5149\u96fb\u5b50\u6a5f\u80fd\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(9) \u30d5\u30a1\u30eb\u30de\u30b7\u30a2\uff0c\u65e5\u672c\u85ac\u5b66\u4f1a\uff0c2009\u5e74, vol. 45, No. 3, p222-226.<\/p>\r\n<p>\u300c\u6709\u6a5f\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u5408\u6210\u3068\u6a5f\u80fd\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\u3001\u4e2d\u6751\u6804\u4e00<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(10) \u6771\u4eac\u5927\u5b66 \u74b0\u5883\u5831\u544a\u66f8\u30002009\u5e74, p37.<\/p>\r\n<p>\u300c\u65b0\u3057\u3044\u30a8\u30cd\u30eb\u30ae\u30fc\u6e90\u3068\u3057\u3066\u306e\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(11) \u74b0\u5883\u5b89\u5168\uff08\u6771\u4eac\u5927\u5b66\u74b0\u5883\u5b89\u5168\u7814\u7a76\u30bb\u30f3\u30bf\u30fc\uff09\u30002010\u5e74, 3\u6708\u53f7, No. 124, p3-6.<\/p>\r\n<p>\u300c\u6709\u6a5f\u7269\u304b\u3089\u306a\u308b\u6b21\u4e16\u4ee3\u592a\u967d\u96fb\u6c60\u3078\u306e\u6311\u6226\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(12) \u6a5f\u80fd\u6750\u6599\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2010\u5e74, vol. 30, No. 2, p52-60.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306b\u7528\u3044\u308b\u65b0\u898f\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53SIMEF\u306e\u958b\u767a\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(13) OHM\uff0c\u30aa\u30fc\u30e0\u793e\uff0c2010\u5e74, vol. 97, p2-3.<\/p>\r\n<p>\u300c\u4f4e\u5206\u5b50\u306e\u5857\u5e03\u3067\u4f5c\u308b\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4f50\u85e4\u4f73\u6674\uff0c\u4e2d\u6751\u6804\u4e00<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(14) Organometallic News\uff0c\u8fd1\u757f\u5316\u5b66\u5354\u4f1a\uff0c2010\u5e74, p30-35.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u958b\u767a\u306b\u304a\u3051\u308b\u5316\u5b66\u7684\u30a2\u30d7\u30ed\u30fc\u30c1\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(15) New Diamond\u3000\u7b2c99\u3000\uff0c\u30cb\u30e5\u30fc\u30c0\u30a4\u30e4\u30e2\u30f3\u30c9\u30d5\u30a9\u30fc\u30e9\u30e0\uff0c2010\u5e74, vol.26, p28-32.<\/p>\r\n<p>\u300c\u65b0\u898f\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u8a2d\u8a08\u3092\u9375\u3068\u3059\u308b\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u7814\u7a76\u958b\u767a\u30fc\u6b74\u53f2\u3068\u6700\u65b0\u306e\u7814\u7a76\u4e8b\u4f8b\u30fc\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(16) \u672a\u6765\u6750\u6599\uff0cNTS\uff0c2011\u5e74, \uff11\u6708\u53f7, vol.11, p55-57.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u5411\u3051\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u958b\u767a\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(17) \u30b7\u30b0\u30de\u30a2\u30eb\u30c9\u30ea\u30c3\u30c1\u30b8\u30e3\u30d1\u30f3\uff0c\u30cb\u30e5\u30fc\u30b9\u30ec\u30bf\u30fc\uff0c\u6750\u6599\u79d1\u5b66\u306e\u57fa\u790e\uff14<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u57fa\u790e\u300d\uff0c\u677e\u5c3e\u3000\u8c4a&nbsp; [<a href=\"http:\/\/www.sigmaaldrich.com\/japan\/materialscience\/catalog.html#MMB\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(18) \u5316\u5b66\u3068\u6559\u80b2\uff0c\u65e5\u672c\u5316\u5b66\u4f1a\uff0c2011\u5e74, vol.59, p242-245.<\/p>\r\n<p>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u3068\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(19) \u5316\u5b66\uff0c\u5316\u5b66\u540c\u4eba\uff0c2011\u5e74, vol.66, No.7, p56-58.<\/p>\r\n<p>\u300c\u52a3\u5316\u3057\u306a\u3044\u9ad8\u6027\u80fd\u6709\u6a5f\u592a\u967d\u96fb\u6c60\u306f\u306f\u305f\u3057\u3066\u5b9f\u73fe\u53ef\u80fd\u304b\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(20) \u5316\u5b66\uff0c\u5316\u5b66\u540c\u4eba\uff0c2011\u5e74, vol.66, No.10, p17-21.<\/p>\r\n<p>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u3068\u9077\u79fb\u91d1\u5c5e\u306e\u7279\u6027\u3092\u6d3b\u304b\u3057\u305f\u5206\u5b50\u30d5\u30a9\u30c8\u30c0\u30a4\u30aa\u30fc\u30c9 -\u5149\u30b3\u30f3\u30d4\u30e5\u30fc\u30bf\u5b9f\u73fe\u3078\u306e\u65b0\u63d0\u6848-\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(21) \u6709\u6a5f\u5206\u5b50\u30fb\u30d0\u30a4\u30aa\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u5206\u79d1\u4f1a\u8a8c\uff0c\u5fdc\u7528\u7269\u7406\u5b66\u4f1a\uff0c2012\u5e74, vol. 23, No.1, pp17-22<\/p>\r\n<p>\u300c\u5857\u5e03\u578b\u4f4e\u5206\u5b50\u8584\u819c\u3092\u7528\u3044\u305f\u6709\u6a5f\u30c7\u30d0\u30a4\u30b9\u306b\u304a\u3051\u308b\u6eb6\u5a92\u548c\u52b9\u679c\u300d\u7530\u4e2d\u79c0\u5e78\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u4e2d\u6751\u6804\u4e00<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(22) Materials Stage\uff0c\u6280\u8853\u60c5\u5831\u5354\u4f1a\uff0c2012\u5e749\u6708\u53f7, p69-71.<\/p>\r\n<p>\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u9178\u5316\u304b&#12441;\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u52a3\u5316\u306b\u53ca\u307b&#12441;\u3059\u5f71\u97ff\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(23) \u5316\u5b66\u5de5\u696d\uff0c\u5316\u5b66\u5de5\u696d\u793e\uff0c2012\u5e74, vol. 63, p40-46.<\/p>\r\n<p>\u300c\u65b0\u898f\u30dd\u30eb\u30d5\u30a3\u30ea\u30f3\u8a98\u5c0e\u4f53\u3092\u7528\u3044\u305f\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u6ce2\u591a\u91ce\u6df3\u4e00\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(24) \u30d5\u30a1\u30a4\u30f3\u30b1\u30df\u30ab\u30eb\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2013\u5e74, vol. 42, No. 1, p35-41.<\/p>\r\n<p>&nbsp;\u300c\u5869\u5316\u7b2c\u4e8c\u9244\u3092\u5229\u7528\u3057\u305f\u7c21\u4fbf\u306a\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210\u65b9\u6cd5\u300d\uff0c\u6a4b\u53e3\u660c\u5f66\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(25) \u5316\u5b66\u3068\u6559\u80b2\uff0c\u65e5\u672c\u5316\u5b66\u4f1a\uff0c2013\u5e74, vol. 61, No. 2, p64&ndash;65.<\/p>\r\n<p>\u300c\u9ad8\u52b9\u7387\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u3092\u6c42\u3081\u3066\u300d\uff0c\u5ca1\u7530\u6d0b\u53f2\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(26) \u6a5f\u80fd\u6750\u6599\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2013\u5e74, vol. 33. No. 3, p20&ndash;25.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306b\u7528\u3044\u3089\u308c\u308b\u96fb\u5b50\u30a2\u30af\u30bb\u30d5&#12442;\u30bf\u30fc\u6750\u6599\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(27) \u6708\u520a\u30c7\u30a3\u30b9\u30d7\u30ec\u30a4\uff0c\u30c6\u30af\u30ce\u30bf\u30a4\u30e0\u30ba\u793e\uff0c2013\u5e74, vol. 19, No. 8, p68&ndash;73.<\/p>\r\n<p>\u300c\u9178\u5316\u3055\u308c\u305f\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u304c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u7279\u6027\u306b\u53ca\u307c\u3059\u5f71\u97ff\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(28) \u5316\u5b66\u5de5\u696d\uff0c\u5316\u5b66\u5de5\u696d\u793e\uff0c2013\u5e74, vol. 64, No. 8, p57&ndash;64.<\/p>\r\n<p>\u300c\u5206\u53d6 HPLC \u306b\u3088\u308b\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u5206\u96e2\u3068\u7cbe\u88fd\u300d\uff0c\u7a32\u7530\u3000\u5bdb\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(29) \u6a5f\u80fd\u6750\u6599\uff0c\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248\uff0c2014\u5e74, vol. 34, No. 1, p46&ndash;51.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306b\u7528\u3044\u308b\u65b0\u898f\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u30e1\u30bf\u30ce\u30a4\u30f3\u30c7\u30f3\u30d5\u30e9\u30fc\u30ec\u30f3\u306e\u958b\u767a\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(30) \u548c\u5149\u7d14\u85ac\u6709\u6a5f\u5316\u5b66\u60c5\u5831\u8a8cOrganic Square\uff0c2014\u5e74, No. 47, p8&ndash;9.<\/p>\r\n<p>\u300c\u30ea\u30c1\u30a6\u30e0\u30a4\u30aa\u30f3\u5185\u5305\u30d5\u30e9\u30fc\u30ec\u30f3Li<sup>+<\/sup>@C<sub>60<\/sub>\u306e\u57fa\u790e\u3068\u5fdc\u7528\u3000\u305d\u306e\uff11\u300d\u9752\u67f3\u3000\u5fcd\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(31) \u96fb\u6c17\u8a08\u7b97\uff0c\u96fb\u6c17\u66f8\u9662\uff0c2014\u5e74\uff0c7\u6708\u53f7\uff0cp38&ndash;44.<\/p>\r\n<p>\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u958b\u767a\u52d5\u5411\u3068\u5c55\u671b\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(32) \u8868\u9762\u79d1\u5b66\uff0c\u65e5\u672c\u8868\u9762\u79d1\u5b66\u4f1a\uff0c2014\u5e74, vol. 35, No. 11, p603&ndash;608.<\/p>\r\n<p>\u300c\u65b0\u898f\u30d5\u30e9\u30fc\u30ec\u30f3\u7cfb\u6750\u6599\u306b\u3088\u308b\u30d0\u30eb\u30af\u30d8\u30c6\u30ed\u30b8\u30e3\u30f3\u30af\u30b7\u30e7\u30f3\u6709\u6a5f\u592a\u967d\u96fb\u6c60\u306e\u52b9\u7387\u5411\u4e0a\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(33) \u30b7\u30b0\u30de\u30a2\u30eb\u30c9\u30ea\u30c3\u30c1\u30b8\u30e3\u30d1\u30f3\uff0c\u6750\u6599\u79d1\u5b66\u306e\u57fa\u790e\uff0c\u82f1\u8a9e\u7248\uff08Materials Matters Basics\uff09Vol.4 [<a href=\"http:\/\/www.sigmaaldrich.com\/content\/dam\/sigma-aldrich\/docs\/SAJ\/Brochure\/1\/j_material-matters-basics-vol4.pdf\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>\u300cFundamentals of Organic Thin Film Solar Cells\u300dYutaka Matsuo<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(34) \u7406\u79d1\u901a\u4fe1\u30b5\u30a4\u30a8\u30f3\u30b9\u30cd\u30c3\u30c8\u7b2c53\u53f7\uff0c\u6570\u7814\u51fa\u7248\uff0c\u8868\u7d19<\/p>\r\n<p>\u300c\u30ab\u30fc\u30dc\u30f3\u30ca\u30ce\u30c1\u30e5\u30fc\u30d6\u3092\u96fb\u6975\u3068\u3059\u308b\u30d5\u30ec\u30ad\u30b7\u30d6\u30eb\u6709\u6a5f\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(35) \u5316\u5b66\u306e\u8981\u70b9\u30b7\u30ea\u30fc\u30ba\u300c\u30d5\u30e9\u30fc\u30ec\u30f3\uff1a\u30b5\u30c3\u30ab\u30fc\u30dc\u30fc\u30eb\u578b\u5206\u5b50\u300d\uff0c\u65e5\u672c\u5316\u5b66\u4f1a\u7de8<\/p>\r\n<p>\u3000\u30b3\u30e9\u30e0\u300c\u592a\u967d\u96fb\u6c60\u3078\u306e\u5fdc\u7528\u6700\u524d\u7dda\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(36) \u7406\u5b66\u90e8\u30cb\u30e5\u30fc\u30b9\uff0c2015\u5e74\uff0cvol. 47\uff0cNo. 3\uff0cp6\uff0e\u300c\u5b66\u90e8\u751f\u306b\u4f1d\u3048\u308b\u7814\u7a76\u6700\u524d\u7dda\u300d\u6b04<\/p>\r\n<p>\u300c\u30ab\u30fc\u30dc\u30f3\u30ca\u30ce\u30c1\u30e5\u30fc\u30d6\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a\uff0c\u7530\u3000\u65e5\u3000[<a href=\"http:\/\/www.s.u-tokyo.ac.jp\/ja\/wp-content\/uploads\/sites\/2\/2015\/09\/20150920_47_3.pdf\" target=\"_blank\">LINK<\/a>]<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(37) \u5316\u5b66\u5de5\u696d\uff0c2016\u5e74\uff0cvol. 67\uff0cNo. 1\uff0cp53&ndash;59.<\/p>\r\n<p>\u300c\u30ea\u30c1\u30a6\u30e0\u30a4\u30aa\u30f3\u5185\u5305\u30d5\u30e9\u30fc\u30ec\u30f3\u3068\u305d\u306e\u5316\u5b66\u300d\uff0c\u5ca1\u7530\u6d0b\u53f2\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(38) OHM\uff0c\u30aa\u30fc\u30e0\u793e\uff0c2016\u5e74, 6\u6708\u53f7\uff0cp65&ndash;67.<\/p>\r\n<p>\u300c\u900f\u660e\u9178\u5316\u30c1\u30bf\u30f3\u96fb\u6975\u3092\u7528\u3044\u305f\u30a4\u30f3\u30b8\u30a6\u30e0\u3092\u542b\u307e\u306a\u3044\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(39) \u5730\u57df\u751f\u6d3b\u5b66\u7814\u7a76\uff0c2016\u5e74\uff0cvol. 7\uff0cp117-126.<\/p>\r\n<p>\u300c\u666f\u89b3\u306b\u9069\u5408\u3059\u308b\u6709\u6a5f\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(40) \u30b1\u30df\u30ab\u30eb\u30a8\u30f3\u30b8\u30cb\u30e4\u30ea\u30f3\u30b0\uff0c2018\u5e74\uff0c9\u6708\u53f7\uff0cp13-18.<\/p>\r\n<p>\u300c\u30ab\u30fc\u30dc\u30f3\u30ca\u30ce\u30c1\u30e5\u30fc\u30d6\u900f\u660e\u96fb\u6975\u3092\u7528\u3044\u305f\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u300d\uff0c\u7530\u3000\u65e5\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(41) \u5206\u6790\u5316\u5b66\uff0c\u65e5\u672c\u5206\u6790\u5316\u5b66\u4f1a\uff0c2018\u5e74\uff0c11\u6708\u53f7<\/p>\r\n<p>\u300c\u5927\u6c17\u4e2d\u5149\u96fb\u5b50\u5206\u5149\u53ce\u91cf\u5206\u5149\u5206\u6790\u306b\u3088\u308b\u6709\u6a5f\u8584\u819c\u534a\u5c0e\u4f53\u306e\u30a8\u30cd\u30eb\u30ae\u30fc\u6e96\u4f4d\u306e\u6e2c\u5b9a\u300d\uff0c\u5c0f\u6c72\u4f73\u7950\uff0c\u85e4\u5dfb\u5eb7\u4eba\uff0c\u4e2d\u5ddd\u8cb4\u6587\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(42) \u592a\u967d\u30a8\u30cd\u30eb\u30ae\u30fc (Journal of Japan Solar Energy Society)\uff0c\u65e5\u672c\u592a\u967d\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\uff0c2019\u5e74\uff0cVol. 45\uff0cNo. 1\uff0cp47-54.<\/p>\r\n<p>\u300c\u30ca\u30ce\u30ab\u30fc\u30dc\u30f3\u6750\u6599\u3092\u6d3b\u7528\u3057\u305f\u30d5\u30ec\u30ad\u30b7\u30d6\u30eb\u3067\u5b89\u5b9a\u306a\u30da\u30ed\u30d6\u30b9\u30ab\u30a4\u30c8\u592a\u967d\u96fb\u6c60\u300d\uff0c\u677e\u5c3e\u3000\u8c4a<\/p>\r\n<p>&nbsp;<\/p>\r\n<div>(43) Merck \u6750\u6599\u79d1\u5b66\u306e\u57fa\u790e\u7b2c 4 \u53f7\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u57fa\u790e\u300d\u4ed8\u9332<\/div>\r\n<p>\u300c\u79d1\u5b66\u6559\u80b2\u3078\u306e\u5fdc\u7528\u300d\uff0c\u677e\u5c3e \u8c4a\uff0c\u4e2d\u5ddd\u8cb4\u6587\uff0c\u68b6\u4e95\u5b8f\u6a39<\/p>\r\n<p><a href=\"https:\/\/www.sigmaaldrich.com\/japan\/materialscience\/catalog\/zknk\/opv.html#appendix\">javascript:mctmp(0);<\/a><\/p>\r\n<p>&nbsp;<\/p>\r\n<p>(44)&nbsp; \u5316\u5b66\uff0c\u5316\u5b66\u540c\u4eba\uff0c2020 \u5e74\uff0c2 \u6708\u53f7 \u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u7814\u7a76\u306e\u30ea\u30d0\u30a4\u30d0\u30eb&ndash;\u7740\u5b9f\u306a\u6539\u826f\u306e\u84c4\u7a4d\u304c\u98db\u8e8d\u3092\u3082\u305f\u3089\u3057\u305f!\u300d\uff0c\u677e\u5c3e \u8c4a<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>\u7279\u8a31\uff08\u56fd\u5185\uff09<\/h4>\r\n<p>(1) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582002-016143\uff0c\u7279\u958b2003-212880\uff0c\u7279\u8a31\u7b2c4109457\u53f7<\/p>\r\n<p>(2) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u91d1\u5c5e\u932f\u4f53<\/p>\r\n<p>\u3000\u7279\u98582002-016144\uff0c\u7279\u958b2003-212881\uff0c\u7279\u8a31\u7b2c4109458\u53f7<\/p>\r\n<p>(3) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582004-157248\uff0c\u7279\u958b2005-015470\uff0c\u7279\u8a31\u7b2c4211682\u53f7<\/p>\r\n<p>(4) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u30d5\u30e9\u30fc\u30ec\u30f3\u91d1\u5c5e\u932f\u4f53\u3001\u4e26\u3073\u306b\u305d\u308c\u3089\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582005-014594\uff0c\u7279\u958b2005-232165\uff0c\u7279\u8a31\u7b2c4636889\u53f7<\/p>\r\n<p>(5) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u30d5\u30e9\u30fc\u30ec\u30f3\u91d1\u5c5e\u932f\u4f53\u3001\u4e26\u3073\u306b\u305d\u308c\u3089\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582005-021961\uff0c\u7279\u958b2006-206522\uff0c\u7279\u8a31\u7b2c4627440\u53f7<\/p>\r\n<p>(6) \u70ad\u7d20-\u70ad\u7d20\u7d50\u5408\u751f\u6210\u53cd\u5fdc\u7528\u89e6\u5a92<\/p>\r\n<p>\u3000\u7279\u98582005-067241\uff0c\u7279\u958b2006-247521<\/p>\r\n<p>(7) \u91d1\u5c5e\u542b\u6709\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\uff0c\u305d\u308c\u3092\u6709\u3059\u308b\u7d44\u6210\u7269\uff0c\u305d\u308c\u3092\u7d44\u7e54\u5316\u3057\u305f\u69cb\u9020\u4f53\uff0c\u4e26\u3073\u306b\uff0c\u305d\u308c\u3092\u7528\u3044\u305f\u6db2\u6676\u30c7\u30a3\u30b9\u30d7\u30ec\u30a4\u6750\u6599\uff0c\u91cf\u5b50\u30c7\u30d0\u30a4\u30b9\u6750\u6599\u53ca\u3073\u5206\u5b50\u30b9\u30a4\u30c3\u30c1\u6750\u6599<\/p>\r\n<p>\u3000\u7279\u98582005-319750\uff0c\u7279\u958b2007-126389<\/p>\r\n<p>(8) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u304a\u3088\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582006-040203\uff0c\u7279\u958b2007-217350\uff0c\u7279\u8a31\u7b2c4699233\u53f7<\/p>\r\n<p>(9) \u5149\u96fb\u5909\u63db\u7d20\u5b50\u304a\u3088\u3073\u305d\u306e\u7d20\u5b50\u3092\u7528\u3044\u305f\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582006-315474\uff0c\u7279\u958b2008-130889\uff0c\u7279\u8a31\u7b2c4875469\u53f7<\/p>\r\n<p>(10) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582007-039836\uff0c\u7279\u958b2008-201721\uff0c\u7279\u8a31\u7b2c4877800\u53f7<\/p>\r\n<p>(11) \u30aa\u30ec\u30d5\u30a3\u30f3\u7528\u91cd\u5408\u89e6\u5a92<\/p>\r\n<p>\u3000\u7279\u98582007-041438\uff0c\u7279\u958b2008-201962\uff0c\u7279\u8a31\u7b2c4953124\u53f7<\/p>\r\n<p>(12) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u304a\u3088\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582007-059740\uff0c\u7279\u958b2008-222583\uff0c\u7279\u8a31\u7b2c4849410\u53f7<\/p>\r\n<p>(13) \u5358\u5206\u5b50\u30c8\u30e9\u30f3\u30b8\u30b9\u30bf\u304a\u3088\u3073\u5358\u96fb\u5b50\u30c8\u30e9\u30f3\u30b8\u30b9\u30bf\u306b\u7528\u3044\u308b\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53<\/p>\r\n<p>\u3000\u7279\u98582007-132739\uff0c\u7279\u958b2008-288421\uff0c\u7279\u8a31\u7b2c5004656\u53f7<\/p>\r\n<p>(14) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582008-123165\uff0c\u7279\u958b2008-231114\uff0c\u7279\u8a31\u7b2c5091760\u53f7<\/p>\r\n<p>(15) \u5149\u96fb\u5909\u63db\u7d20\u5b50\u304a\u3088\u3073\u305d\u306e\u7d20\u5b50\u3092\u7528\u3044\u305f\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582008-174166\uff0c\u7279\u958b2009-206470\uff0c\u7279\u8a31\u7b2c5548933\u53f7<\/p>\r\n<p>(16) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53<\/p>\r\n<p>\u3000\u7279\u98582008-503749\uff0cWO2007102255\uff0c\u7279\u8a31\u7b2c4988702\u53f7<\/p>\r\n<p>(17) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u304a\u3088\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582008-507459\uff0cWO2007-111226\uff0c\u7279\u8a31\u7b2c4942220\u53f7<\/p>\r\n<p>(18) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u3092\u542b\u3080\u5149\u96fb\u5909\u63db\u6750\u6599<\/p>\r\n<p>\u3000\u7279\u98582008-514530\uff0cWO2007129767\uff0c\u7279\u8a31\u7b2c5062765\u53f7<\/p>\r\n<p>(19) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u3092\u542b\u3080\u5149\u96fb\u5909\u63db\u6750\u6599<\/p>\r\n<p>\u3000\u7279\u98582008-514531\uff0cWO2007129768\uff0c\u7279\u8a31\u7b2c5062766\u53f7<\/p>\r\n<p>(20) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582008-544124\uff0cWO2008-059771\uff0c\u7279\u8a31\u7b2c5246699\u53f7<\/p>\r\n<p>(21) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582009-051894\uff0c\u7279\u958b2010-202611\uff0c\u7279\u8a31\u7b2c5142221\u53f7<\/p>\r\n<p>(22) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u304a\u3088\u3073\u5f53\u8a72\u8a98\u5c0e\u4f53\u3092\u542b\u3080\u5149\u96fb\u5909\u63db\u6750\u6599<\/p>\r\n<p>\u3000\u7279\u98582009-121429\uff0c\u7279\u958b2010-270018\uff0c\u7279\u8a31\u7b2c5072044\u53f7<\/p>\r\n<p>(23) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\uff0c\u534a\u5c0e\u4f53\u6750\u6599\uff0c\u5149\u96fb\u5909\u63db\u7d20\u5b50\u53ca\u3073\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582009-254456\uff0c\u7279\u958b2011-098906\uff0c\u7279\u8a31\u7b2c5531241\u53f7<\/p>\r\n<p>(24) \u534a\u5c0e\u4f53\u30c7\u30d0\u30a4\u30b9\u306e\u88fd\u9020\u65b9\u6cd5\u53ca\u3073\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582010-012546\uff0c\u7279\u958b2010-192891\uff0c\u7279\u8a31\u7b2c5531243\u53f7<\/p>\r\n<p>(25) \u30d5\u30e9\u30fc\u30ec\u30f3\u4e8c\u91cf\u4f53\u304a\u3088\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582010-049276\uff0c\u7279\u958b2011-184326\uff0c\u7279\u8a31\u7b2c5633873\u53f7<\/p>\r\n<p>(26) \u96fb\u8377\u8f38\u9001\u6750\u6599\uff0c\u305d\u308c\u3092\u7528\u3044\u305f\u8584\u819c\u53ca\u3073\u6709\u6a5f\u96fb\u5b50\u30c7\u30d0\u30a4\u30b9\uff0c\u4e26\u3073\u306b\u30d1\u30a4\u96fb\u5b50\u7cfb\u5316\u5408\u7269<\/p>\r\n<p>\u3000\u7279\u98582010-054572\uff0c\u7279\u958b2011-187893\uff0c\u7279\u8a31\u7b2c5574410\u53f7<\/p>\r\n<p>(27) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u30d5\u30e9\u30fc\u30ec\u30f3\u91d1\u5c5e\u932f\u4f53\u3001\u4e26\u3073\u306b\u305d\u308c\u3089\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582010-224661\uff0c\u7279\u958b2011-026339\uff0c\u7279\u8a31\u7b2c5265640\u53f7<\/p>\r\n<p>(28) \u5149\u96fb\u5909\u63db\u7d20\u5b50\u304a\u3088\u3073\u305d\u306e\u7d20\u5b50\u3092\u7528\u3044\u305f\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582011-183531\uff0c\u7279\u958b2011-258980\uff0c\u7279\u8a31\u7b2c5435508\u53f7<\/p>\r\n<p>(29) \u5149\u96fb\u5909\u63db\u7d20\u5b50\uff0c\u30d5\u30e9\u30fc\u30ec\u30f3\u5316\u5408\u7269\u306e\u88fd\u9020\u65b9\u6cd5\uff0c\u53ca\u3073\u30d5\u30e9\u30fc\u30ec\u30f3\u5316\u5408\u7269<\/p>\r\n<p>\u3000\u7279\u98582011-192064\uff0c\u7279\u958b2012-094829\uff0c\u7279\u8a31\u7b2c5822117\u53f7<\/p>\r\n<p>(30) \u30d5\u30e9\u30fc\u30ec\u30f3C60\u8a98\u5c0e\u4f53\uff0c\u4e26\u3073\u306b\u6975\u7d2b\u5916\u7dda\u5149\u53c8\u306f\u96fb\u5b50\u30d3\u30fc\u30e0\u9732\u5149\u7528\u30ec\u30b8\u30b9\u30c8\u7d44\u6210\u7269<\/p>\r\n<p>\u3000\u7279\u98582012-250116\uff0c\u7279\u958b2014-097965\uff0c\u7279\u8a31\u7b2c6044283\u53f7<\/p>\r\n<p>(31) \u30ab\u30fc\u30dc\u30f3\u30ca\u30ce\u30c1\u30e5\u30fc\u30d6\u6709\u6a5f\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582014-178204\uff0cWO2016-035832<\/p>\r\n<p>(32) \u30a2\u30af\u30ea\u30b8\u30f3\u7cfb\u5316\u5408\u7269\u304a\u3088\u3073\u3053\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u8584\u819c\u30c7\u30d0\u30a4\u30b9<\/p>\r\n<p>\u3000\u7279\u98582015-008622\uff0c\u7279\u958b2016-132642\uff0c\u7279\u8a31\u7b2c6471998\u53f7<\/p>\r\n<p>(33) \u30cb\u30aa\u30d6\u30c9\u30fc\u30d7\u9178\u5316\u30c1\u30bf\u30f3\u3092\u7528\u3044\u305f\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60<\/p>\r\n<p>\u3000\u7279\u98582015-034346\uff0c\u7279\u958b2016-157810<\/p>\r\n<p>(34) \u82b3\u9999\u65cf\u70ad\u5316\u6c34\u7d20\u307e\u305f\u306f\u82b3\u9999\u65cf\u8907\u7d20\u74b0\u306e\u9aa8\u683c\u3092\u6709\u3059\u308b\u30a2\u30df\u30ce\u57fa\u307e\u305f\u306f\u30a2\u30eb\u30ad\u30eb\u30a2\u30df\u30ce\u57fa\u542b\u6709\u5316\u5408\u7269\u304a\u3088\u3073\u3053\u308c\u3092\u7528\u3044\u305f\u6709\u6a5f\u8584\u819c\u30c7\u30d0\u30a4\u30b9<\/p>\r\n<p>\u3000\u7279\u98582016-181196\uff0c\u7279\u958b2018-046219<\/p>\r\n<p>(35) \u65b0\u898f\u306a\u30dd\u30eb\u30d5\u30a3\u30ea\u30f3\u8a98\u5c0e\u4f53\uff0c\u30dd\u30eb\u30d5\u30a3\u30ea\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5\uff0c\u30c9\u30ca\u30fc\u6750\u6599\uff0c\u5149\u96fb\u5909\u63db\u88c5\u7f6e\uff0c\u304a\u3088\u3073\u5149\u96fb\u5909\u63db\u88c5\u7f6e\u306e\u88fd\u9020\u65b9\u6cd5<\/p>\r\n<p>\u3000\u7279\u98582018-117844<\/p>\r\n<p>(36) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u305d\u308c\u3092\u542b\u3080\u8584\u819c\uff0c\u5149\u96fb\u7d20\u5b50\u4e26\u3073\u306b\u30a4\u30e1\u30fc\u30b8\u30bb\u30f3\u30b5\u30fc\u53ca\u3073\u96fb\u5b50\u88c5\u7f6e<\/p>\r\n<p>\u3000\u7279\u98582018-223297\uff0c\u7279\u958b2019-99570<\/p>\r\n<p>(37) \uff2e&minus;\u578b\u534a\u5c0e\u4f53\u7d44\u6210\u7269\u4e26\u3073\u306b\u3053\u308c\u3092\u542b\u3080\u8584\u819c\u3001\u6709\u6a5f\u5149\u96fb\u7d20\u5b50\u3001\u30a4\u30e1\u30fc\u30b8\u30bb\u30f3\u30b5\u30fc\u53ca\u3073\u96fb\u5b50\u88c5\u7f6e<\/p>\r\n<p>\u7279\u9858 2020-86343\uff0c\u7279\u958b 2020-188260<\/p>\r\n<p>(38) \u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u3001\u30d5\u30e9\u30fc\u30ec\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5\u3001\u84b8\u7740\u7269\u3001\u819c\u3001\u53ca\u3073\u96fb\u5b50\u30c7\u30d0\u30a4\u30b9<\/p>\r\n<p>\u7279\u9858 2020-009133<\/p>\r\n<p>(39) \u30d5\u30eb\u30aa\u30ec\u30cb\u30ea\u30c7\u30f3&minus;\u30a2\u30af\u30ea\u30c0\u30f3\u8a98\u5c0e\u4f53\u3001\u30d5\u30eb\u30aa\u30ec\u30cb\u30ea\u30c7\u30f3&minus;\u30a2\u30af\u30ea\u30c0\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u65b9\u6cd5\u3001\u30e1\u30ab<\/p>\r\n<p>\u30ce\u30af\u30ed\u30df\u30ba\u30e0\u6750\u6599\u3001\u96fb\u8377\u8f38\u9001\u6750\u6599\u3001\u53ca\u3073\u96fb\u5b50\u30c7\u30d0\u30a4\u30b9<\/p>\r\n<\/div>\r\n\r\n<div class=\"block\">\r\n<h4>\u7279\u8a31\uff08\u6d77\u5916\uff0c\u7279\u5b9a\u56fd\uff09<\/h4>\r\n<p>(1) \u7c73\u56fd\u7279\u8a31\uff1aUS 6,969,772<\/p>\r\n<p>(2) \u7c73\u56fd\u7279\u8a31\uff1aUS 7,202,374<\/p>\r\n<p>(3) \u7c73\u56fd\u7279\u8a31\uff1aUS 7,547,429<\/p>\r\n<p>(4) \u7c73\u56fd\u7279\u8a31\uff1aUS 7,790,913<\/p>\r\n<p>(5) \u7c73\u56fd\u7279\u8a31\uff1aUS 8,134,019<\/p>\r\n<p>(6) \u7c73\u56fd\u7279\u8a31\uff1aUS 8,153,835<\/p>\r\n<p>(7) \u7c73\u56fd\u7279\u8a31\uff1aUS 8,304,643<\/p>\r\n<p>(8) \u4e2d\u56fd\u7279\u8a31\uff1aCN 101405252<\/p>\r\n<p>(9) \u4e2d\u56fd\u7279\u8a31\uff1aCN 101535220<\/p>\r\n<p>(10) \u4e2d\u56fd\u7279\u8a31\uff1aCN 101689611<\/p>\r\n<p>(11) \u53f0\u6e7e\u7279\u8a31\uff1a\u7b2c I 462361\u53f7<\/p>\r\n<p>(12) \u97d3\u56fd\u7279\u8a31\uff1a10-2017-0088287<\/p>\r\n<p>(13) \u97d3\u56fd\u7279\u8a31\uff1a10-2017-0165360<\/p>\r\n<p>(14) \u97d3\u56fd\u7279\u8a31\uff1a10-2018-0141753<\/p>\r\n<\/div>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Member \u677e\u5c3e \u8c4a Education 1992\u20131996 Department of Chemistry, Faculty of Engineering Science, Osaka UniversityAward 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