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dc.contributor.authorHansen, JA
dc.contributor.authorBecher, J
dc.contributor.authorJeppesen, JO
dc.contributor.authorLevillain, E
dc.contributor.authorNielsen, MB
dc.contributor.authorPetersen, BM
dc.contributor.authorŞahin, Y
dc.date.accessioned2019-10-20T09:30:55Z
dc.date.available2019-10-20T09:30:55Z
dc.date.issued2004
dc.identifier.issn0959-9428
dc.identifier.issn1364-5501
dc.identifier.urihttps://dx.doi.org/10.1039/b310733g
dc.identifier.urihttps://hdl.handle.net/11421/17516
dc.descriptionWOS: 000187918100009en_US
dc.description.abstractThe synthesis of novel donor-pi-acceptor dyads based on a pyrrolo-annelated tetrathiafulvalene unit is described. The linear and non-linear optical properties of these chromophores have been investigated, together with their redox properties. For a dyad containing a p-nitrophenyl acceptor group, a significant third-order optical non-linearity is observed.en_US
dc.language.isoengen_US
dc.publisherRoyal Soc Chemistryen_US
dc.relation.isversionof10.1039/b310733gen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSynthesis and non-linear optical properties of monopyrrolotetrathiafulvalene derived donor-pi-acceptor dyadsen_US
dc.typearticleen_US
dc.relation.journalJournal of Materials Chemistryen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.volume14en_US
dc.identifier.issue2en_US
dc.identifier.startpage179en_US
dc.identifier.endpage184en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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