{"id":757,"date":"2007-12-19T16:36:24","date_gmt":"2007-12-19T20:36:24","guid":{"rendered":"http:\/\/softbeam.net\/research\/?p=757"},"modified":"2007-12-19T16:36:24","modified_gmt":"2007-12-19T20:36:24","slug":"implementation-of-a-hamiliton-receptor-based-hydrogen-bonding-motif-toward-a-new-electron-donor-acceptor-prototype-electron-versus-energy-transfer","status":"publish","type":"post","link":"https:\/\/softbeam.net\/research\/?p=757","title":{"rendered":"Implementation of a Hamiliton-Receptor-Based Hydrogen-Bonding Motif toward a New Electron Donor-Acceptor Prototype: Electron versus Energy Transfer"},"content":{"rendered":"<p><a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2007\/12\/jacs-07-hamiliton-receptor-based-tpp-fullerene-for-electron-energy-transfer.PDF\">Florian Wessendorf, Jan-Frederik Gnichwitz, Ginka H. Sarova, Kristine Hager, Uwe Hartnagel, Dirk M. Guldi,* and Andreas Hirsch*<\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2007\/12\/jacs-07-hamiliton-receptor-based-tpp-fullerene-for-electron-energy-transfer.PDF\">J. AM. CHEM. SOC. 2007, 129, 16057 16071 <\/a><br \/>\nand in the same issue a similar dyads with chemical instead of physical bonding:<br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2007\/12\/jacs-07-azobenzene-linked-porphyrin-fullerene-dyads.PDF\">Azobenzene-Linked Porphyrin-Fullerene Dyads<\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2007\/12\/jacs-07-azobenzene-linked-porphyrin-fullerene-dyads.PDF\">J. AM. CHEM. SOC. 2007, 129, 15973 15982<\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2007\/12\/jacs-07-azobenzene-linked-porphyrin-fullerene-dyads.PDF\">David I. Schuster,* Ke Li, Dirk M. Guldi,* Amit Palkar, Luis Echegoyen, Christopher Stanisky, R. James Cross, Marja Niemi, Nikolai V. Tkachenko, and Helge Lemmetyinen<\/a><br \/>\nand a former research on dyads:<br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2008\/01\/jacs-96-electron-transfer-in-zincporphyrin-c60-dyads.PDF\">Linkage and Solvent Dependence of Photoinduced Electron Transfer in Zincporphyrin-C60 Dyads<\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2008\/01\/jacs-96-electron-transfer-in-zincporphyrin-c60-dyads.PDF\">Hiroshi Imahori, Kiyoshi Hagiwara, Masanori Aoki, Tsuyoshi Akiyama, Seiji Taniguchi, Tadashi Okada,* Masahiro Shirakawa, and Yoshiteru Sakata* <\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2008\/01\/jacs-96-electron-transfer-in-zincporphyrin-c60-dyads.PDF\">J. Am. Chem. Soc. 1996, 118, 11771-11782<\/a><br \/>\nand other porphyrin dyad:<br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2008\/01\/chemeur-99-porphyrin-flavin-dyad.PDF\">Synthesis, Spectroscopy, and Semiempirical Study of a Novel Porphyrin \u00e2\u20ac\u201c Flavin Dyad<\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2008\/01\/chemeur-99-porphyrin-flavin-dyad.PDF\">Dominik T. Hermann, Anne Christina Schindler, Kurt Polborn, Rudolf Gompper, Susanne Stark, Andreas B. J. Parusel, Gottfried Grabner, and Gottfried K\u00c3\u00b6hler* <\/a><br \/>\n<a href=\"http:\/\/20.210.105.67\/research\/wp-content\/uploads\/2008\/01\/chemeur-99-porphyrin-flavin-dyad.PDF\">Chem. Eur. J. 1999, 5, No. 11, 3208<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Florian Wessendorf, Jan-Frederik Gnichwitz, Ginka H. Sarova, Kristine Hager, Uwe Hartnagel, Dirk M. Guldi,* and Andreas Hirsch* J. AM. CHEM. SOC. 2007, 129, 16057 16071 and in the same issue a similar dyads with chemical instead of physical bonding: Azobenzene-Linked Porphyrin-Fullerene Dyads J. AM. CHEM. SOC. 2007, 129, 15973 15982 David I. Schuster,* Ke Li, &hellip; <a href=\"https:\/\/softbeam.net\/research\/?p=757\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Implementation of a Hamiliton-Receptor-Based Hydrogen-Bonding Motif toward a New Electron Donor-Acceptor Prototype: Electron versus Energy Transfer&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2,4,6],"tags":[],"class_list":["post-757","post","type-post","status-publish","format-standard","hentry","category-beam","category-energetics","category-optoelectronics"],"_links":{"self":[{"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=\/wp\/v2\/posts\/757","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=757"}],"version-history":[{"count":0,"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=\/wp\/v2\/posts\/757\/revisions"}],"wp:attachment":[{"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=757"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=757"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/softbeam.net\/research\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=757"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}