Induction and control of supramolecular chirality by light in self-assembled helical nanostructures

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dc.contributor.authorKim, Ji Sungko
dc.contributor.authorLee, Jin Heeko
dc.contributor.authorKim, Woo Youngko
dc.contributor.authorKim, Hyungjunko
dc.contributor.authorLee, Sanghwako
dc.contributor.authorLee, Hee-Chulko
dc.contributor.authorLee, Yoon-Supko
dc.contributor.authorSeo, Myung-Eunko
dc.contributor.authorKim, Sang-Youlko
dc.date.accessioned2015-06-04T01:45:12Z-
dc.date.available2015-06-04T01:45:12Z-
dc.date.created2015-06-01-
dc.date.created2015-06-01-
dc.date.created2015-06-01-
dc.date.created2015-06-01-
dc.date.created2015-06-01-
dc.date.issued2015-04-
dc.identifier.citationNATURE COMMUNICATIONS, v.6-
dc.identifier.issn2041-1723-
dc.identifier.urihttp://hdl.handle.net/10203/198760-
dc.description.abstractEvolution of supramolecular chirality from self-assembly of achiral compounds and control over its handedness is closely related to the evolution of life and development of supramolecular materials with desired handedness. Here we report a system where the entire process of induction, control and locking of supramolecular chirality can be manipulated by light. Combination of triphenylamine and diacetylene moieties in the molecular structure allows photoinduced self-assembly of the molecule into helical aggregates in a chlorinated solvent by visible light and covalent fixation of the aggregate via photopolymerization by ultraviolet light, respectively. By using visible circularly polarized light, the supramolecular chirality of the resulting aggregates is selectively and reversibly controlled by its rotational direction, and the desired supramolecular chirality can be arrested by irradiation with ultraviolet circularly polarized light. This methodology opens a route to ward the formation of supramolecular chiral conducting nanostructures from the self-assembly of achiral molecules.-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleInduction and control of supramolecular chirality by light in self-assembled helical nanostructures-
dc.typeArticle-
dc.identifier.wosid000353704700011-
dc.identifier.scopusid2-s2.0-84928577211-
dc.type.rimsART-
dc.citation.volume6-
dc.citation.publicationnameNATURE COMMUNICATIONS-
dc.identifier.doi10.1038/ncomms7959-
dc.contributor.localauthorLee, Hee-Chul-
dc.contributor.localauthorLee, Yoon-Sup-
dc.contributor.localauthorSeo, Myung-Eun-
dc.contributor.localauthorKim, Sang-Youl-
dc.contributor.nonIdAuthorKim, Woo Young-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCIRCULARLY-POLARIZED LIGHT-
dc.subject.keywordPlusHYBRID DENSITY FUNCTIONALS-
dc.subject.keywordPlusENANTIOMERIC EXCESS-
dc.subject.keywordPlusCOLUMNAR STACKS-
dc.subject.keywordPlusVISIBLE-LIGHT-
dc.subject.keywordPlusORGANIC GELS-
dc.subject.keywordPlusAMPLIFICATION-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusDIACETYLENE-
dc.subject.keywordPlusMOLECULES-
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