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dc.contributor.authorFátima Aparicio-
dc.contributor.authorSandeep Cherumukkil-
dc.contributor.authorAjayaghosh, Ayyappanpillai-
dc.contributor.authorLuis Sánchez-
dc.date.accessioned2016-07-21T05:04:11Z-
dc.date.available2016-07-21T05:04:11Z-
dc.date.issued2015-12-08-
dc.identifier.citationLangmuir 2016, 32, 284−289en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2361-
dc.description.abstract: The synthesis of three cyano-substituted divinylene π- 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 gelators 1−3 that is governed by a cooperative mechanism. A complete set of photophysical parameters (ΦF,τ, kr and knr) demonstrate the role of the molecular aggregation in enhanced emission upon self-assembly.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.titleColor-Tunable Cyano-Substituted Divinylene Arene Luminogens as Fluorescent π‑Gelatorsen_US
dc.typeArticleen_US
Appears in Collections:2016

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