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 |