Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1999
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dc.contributor.authorSaha, Tanmoyen_US
dc.contributor.authorSengupta, Abhigyanen_US
dc.contributor.authorHAZRA, PARTHAen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2019-02-25T09:02:43Z
dc.date.available2019-02-25T09:02:43Z
dc.date.issued2014-07en_US
dc.identifier.citationPhotochemical and Photobiological Sciences, 13(10), 1427-1433.en_US
dc.identifier.issn1474-905Xen_US
dc.identifier.issn1474-9092en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1999-
dc.identifier.urihttps://doi.org/10.1039/C4PP00097Hen_US
dc.description.abstractPyranine 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.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectIn vitro sensingen_US
dc.subjectGreen fluorescenceen_US
dc.subjectPyranineen_US
dc.subjectStoichiometry of Complexationen_US
dc.subjectVoltammetric studies.en_US
dc.subject2014en_US
dc.titleIn vitro sensing of Cu+ through a green fluorescence rise of pyranineen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitlePhotochemical and Photobiological Sciencesen_US
dc.publication.originofpublisherForeignen_US
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