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dc.contributor.authorAjayaghosh, A-
dc.contributor.authorPriya Carol-
dc.contributor.authorSreejith, S-
dc.date.accessioned2014-04-17T08:36:40Z-
dc.date.available2014-04-17T08:36:40Z-
dc.date.issued2005-
dc.identifier.citationJournal of the American Chemical Society 127(43):14962-14963; Nov 2005en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1324-
dc.description.abstractA simple ratiometric fluorescence probe based on vinylpyrrole end-capped bipyridine for the visual sensing of Zn2+ under aqueous physiological pH (6.8-7.4) is described. The fluorophores 3a-c showed strong emission around 537 nm in acetonitrile with a quantum yield of 0.4. In buffered (HEPES, pH 7.2) acetonitrile-water mixture (9:1 v/v), titration of transition metal salts to 3c showed strong quenching of the emission at 547 nm except in the case of Zn2+, which resulted in a red-shifted emission at 637 nm. Alkali and alkaline earth metal salts could not induce any considerable changes to the emission behavior of 3a-c. The binding of Zn2+ was highly selective in the presence of a variety of other metal ions. Though Cu2+ quenches the emission of 3c, in the presence of Zn2+, a red emission prevails, indicating the preference of 3c toward Zn2+. Job plot and Benesi-Hildebrand analysis revealed a 1:1 complexation between the probe and the metal ion. The selective visual sensing of Zn2+ with a red emission is ideally suited for the imaging of biological specimens.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectConjugated polymersen_US
dc.subjectEnhanced fluorescenceen_US
dc.subjectSensor moleculesen_US
dc.subjectZincen_US
dc.subjectBispyrrolesen_US
dc.subjectFoldameren_US
dc.titleA ratiometric fluorescence probe for selective visual sensing of Zn2+en_US
dc.typeArticleen_US
Appears in Collections:2005

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