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dc.contributor.authorShunichi Fukuzumi*
dc.date.accessioned2016-08-28T12:08:27Z-
dc.date.available2016-08-28T12:08:27Z-
dc.date.issued2012*
dc.identifier.issn1359-7345*
dc.identifier.otherOAK-8834*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/222692-
dc.description.abstractA new ZnPc-PDI dyad presenting for the first time a charge-separated state lower in energy than the triplet excited state of the ZnPc and PDI has been synthesized. The rational design implies the substitution of the ZnPc with phenoxy groups and the bay substitution of the PDI with sulfonyl substituents. The lifetime of the charge-separated state was 72 μs. © The Royal Society of Chemistry 2012.*
dc.languageEnglish*
dc.titleRational design of a phthalocyanine-perylenediimide dyad with a long-lived charge-separated state*
dc.typeArticle*
dc.relation.issue50*
dc.relation.volume48*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage6241*
dc.relation.lastpage6243*
dc.relation.journaltitleChemical Communications*
dc.identifier.doi10.1039/c2cc31087b*
dc.identifier.wosidWOS:000304486800010*
dc.identifier.scopusid2-s2.0-84861638915*
dc.author.googleBlas-Ferrando V.M.*
dc.author.googleOrtiz J.*
dc.author.googleBouissane L.*
dc.author.googleOhkubo K.*
dc.author.googleFukuzumi S.*
dc.author.googleFernandez-Lazaro F.*
dc.author.googleSastre-Santos A.*
dc.contributor.scopusidShunichi Fukuzumi(35430038100;58409757400)*
dc.date.modifydate20240401081001*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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