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In vitro sensing of Cu+ through a green fluorescence rise of pyranine

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dc.contributor.author Saha, Tanmoy en_US
dc.contributor.author Sengupta, Abhigyan en_US
dc.contributor.author HAZRA, PARTHA en_US
dc.contributor.author TALUKDAR, PINAKI en_US
dc.date.accessioned 2019-02-25T09:02:43Z
dc.date.available 2019-02-25T09:02:43Z
dc.date.issued 2014-07 en_US
dc.identifier.citation Photochemical and Photobiological Sciences, 13(10), 1427-1433. en_US
dc.identifier.issn 1474-905X en_US
dc.identifier.issn 1474-9092 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1999
dc.identifier.uri https://doi.org/10.1039/C4PP00097H en_US
dc.description.abstract Pyranine as a new class of fluorescent chemosensor for the Cu+ ion is reported. The probe is capable of discriminating ranges of cations from the Cu+ ion, even in competing environment. The dye displayed a rapid fluorescence response (t1/2 = 1.66 min) towards the Cu+ ion, and the micromolar detection limit enabled the detection of the ion in environmental samples. The observed stoichiometry of complexation between pyranine and Cu+ was 2 : 1. Interestingly, the sensing characteristic was specific to only neutral pH. A metal-to-ligand charge-transfer (MLCT)-based mechanism of sensing was proposed based on electron spin resonance (EPR), Raman spectroscopic and cyclic voltammetric studies. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject In vitro sensing en_US
dc.subject Green fluorescence en_US
dc.subject Pyranine en_US
dc.subject Stoichiometry of Complexation en_US
dc.subject Voltammetric studies. en_US
dc.subject 2014 en_US
dc.title In vitro sensing of Cu+ through a green fluorescence rise of pyranine en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Photochemical and Photobiological Sciences en_US
dc.publication.originofpublisher Foreign en_US


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