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dc.contributor.authorFatima Aparicio-
dc.contributor.authorSandeep Cherumukkil-
dc.contributor.authorAjayaghosh, A-
dc.contributor.authorLuis Sanchez-
dc.date.accessioned2016-08-22T09:32:56Z-
dc.date.available2016-08-22T09:32:56Z-
dc.date.issued2016-
dc.identifier.citationLangmuir 32: 284−289en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2401-
dc.description.abstractThe synthesis of three cyano-substituted divinyleneπ-gelators is reported. The modulation of the color is achieved by placing the cyano groups in appropriate position of the conjugated backbone, thus modulating the donor−acceptor interaction. Variable-temperature UV−vis data have been utilized to investigate the self-assembly of the gelators1−3that is governed by a cooperative mechanism. A complete set of photophysical parameters (ΦF ,τ, kr andknr) demonstrate the role of the molecular aggregation in enhanced emission upon self-assemblyen_US
dc.language.isoenen_US
dc.publisherACS publicationen_US
dc.subjectdonor−acceptoren_US
dc.subjectcooperativeen_US
dc.subjectappropriate positionen_US
dc.subjectself-assemblyen_US
dc.subjectmodulationen_US
dc.titleColor-Tunable Cyano-Substituted Divinylene Arene Luminogens as Fluorescentπ‑Gelatorsen_US
dc.typeArticleen_US
Appears in Collections:2016

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