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dc.contributor.authorWijesinghe, Channa A.
dc.contributor.authorEl-Khouly, Mohamed E.
dc.contributor.authorZandler, Melvin E.
dc.contributor.authorFukuzumi, Shunichi
dc.contributor.authorD'Souza, Francis
dc.date.accessioned2013-08-12T17:59:48Z
dc.date.available2013-08-12T17:59:48Z
dc.date.issued2013-07-15
dc.identifier.citationWijesinghe, C. A., El-Khouly, M. E., Zandler, M. E., Fukuzumi, S. and D'Souza, F. (2013), A Charge-Stabilizing, Multimodular, Ferrocene–Bis(triphenylamine)–Zinc-porphyrin–Fullerene Polyad. Chem. Eur. J., v.19:no.29:pp.9629–9638en_US
dc.identifier.issn0947-6539
dc.identifier.otherWOS:000321431600034
dc.identifier.urihttp://dx.doi.org/10.1002/chem.201300877
dc.identifier.urihttp://hdl.handle.net/10057/6134
dc.descriptionClick on the DOI link to access the article (may not be free).en_US
dc.description.abstractA novel multimodular donor-acceptor polyad featuring zinc porphyrin, fullerene, ferrocene, and triphenylamine entities was designed, synthesized, and studied as a charge-stabilizing, photosynthetic-antenna/reaction-center mimic. The ferrocene and fullerene entities, covalently linked to the porphyrin ring, were distantly separated to accomplish the charge-separation/hole-migration events leading to the creation of a long-lived charge-separated state. The geometry and electronic structures of the newly synthesized compound was deduced by B3LYP/3-21G(*) optimization, while the energy levels for different photochemical events was established using data from the optical absorption and emission, and electrochemical studies. Excitation of the triphenylamine entities revealed singlet-singlet energy transfer to the appended zinc porphyrin. As predicted from the energy levels, photoinduced electron transfer from both the singlet and triplet excited states of the zinc porphyrin to fullerene followed by subsequent hole migration involving ferrocene was witnessed from the transient absorption studies. The charge-separated state persisted for about 8.5s and was governed by the distance between the final charge-transfer product, that is, a species involving a ferrocenium cation and a fullerene radical anion, with additional influence from the charge-stabilizing triphenylamine entities located on the zinc-porphyrin macrocycle.en_US
dc.description.sponsorshipNational Science Foundation (Grant Nos. 1110942 and EPS-0903806) and matching support from the State of Kansas through Kansas Technology Enterprise Corporation, a Grant-in-Aid (Nos. 20108010 and 21750146) and the Global COE (center of excellence) program "Global Education and Research Center for Bio-Environmental Chemistry" of Osaka University from Ministry of Education, Culture, Sports, Science and Technology, Japan, KOSEF/MEST through WCU project (R31-2008-000-10010-0) from Korea.en_US
dc.language.isoen_USen_US
dc.publisherWILEY-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.relation.ispartofseriesChemistry - A European Journal;v.19:no.29
dc.subjectArtificial photosynthesisen_US
dc.subjectElectron transferen_US
dc.subjectFerroceneen_US
dc.subjectFullereneen_US
dc.subjectPorphyrinoiden_US
dc.subjectZincen_US
dc.titleA charge-stabilizing, multimodular, ferrocene-bis(triphenylamine)-zinc-porphyrin-fullerene polyaden_US
dc.typeArticleen_US
dc.description.versionPeer reviewed
dc.rights.holderCopyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim


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