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dc.contributor.authorShunichi Fukuzumi*
dc.date.accessioned2016-08-28T12:08:39Z-
dc.date.available2016-08-28T12:08:39Z-
dc.date.issued2010*
dc.identifier.issn0036-8075*
dc.identifier.otherOAK-6859*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221020-
dc.description.abstractIon binding often mediates electron transfer in biological systems as a cofactor strategy, either as a promoter or as an inhibitor. However, it has rarely, if ever, been exploited for that purpose in synthetic host-guest assemblies. We report here that strong binding of specific anions (chloride, bromide, and methylsulfate but not tetrafluoroborate or hexafluorophosphate) to a tetrathiafulvalene calix[4]pyrrole (TTF-C4P) donor enforces a host conformation that favors electron transfer to a bisimidazolium quinone (BIQ 2+) guest acceptor. In contrast, the addition of a tetraethylammonium cation, which binds more effectively than the BIQ 2+ guest in the TTF-C4P cavity, leads to back electron transfer, restoring the initial oxidation states of the donor and acceptor pair. The products of these processes were characterized via spectroscopy and x-ray crystallography.*
dc.languageEnglish*
dc.titleIon-mediated electron transfer in a supramolecular donor-acceptor ensemble*
dc.typeArticle*
dc.relation.issue5997*
dc.relation.volume329*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1324*
dc.relation.lastpage1327*
dc.relation.journaltitleScience*
dc.identifier.doi10.1126/science.1192044*
dc.identifier.wosidWOS:000281657300033*
dc.identifier.scopusid2-s2.0-77956554232*
dc.author.googlePark J.S.*
dc.author.googleKarnas E.*
dc.author.googleOhkubo K.*
dc.author.googleChen P.*
dc.author.googleKadish K.M.*
dc.author.googleFukuzumi S.*
dc.author.googleBielawski C.W.*
dc.author.googleHudnall T.W.*
dc.author.googleLynch V.M.*
dc.author.googleSessler J.L.*
dc.contributor.scopusidShunichi Fukuzumi(35430038100;58409757400)*
dc.date.modifydate20240401081001*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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