Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4720
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dc.contributor.authorKumar H.M.S
dc.contributor.authorKunabenchi R.S
dc.contributor.authorNishti S.V
dc.contributor.authorBiradar J.S
dc.contributor.authorKadadevarmath J.S.
dc.date.accessioned2020-06-12T15:04:38Z-
dc.date.available2020-06-12T15:04:38Z-
dc.date.issued2009
dc.identifier.citationSpectroscopy Letters , Vol. 42 , 5 , p. 226 - 234en_US
dc.identifier.uri10.1080/00387010902895020
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4720-
dc.description.abstractThe fluorescence quenching of solutes 3-[5?-methyl-3?-phenylindol-2?-yl]-s-triazolo [3,4-b] [1,3,4] thiadiazol-6(5H)-thione (MPITTT) and 3-phenyl-2,5-bis-[thiosemicarbazido] indole (PbisTI) by carbon tetra- chloride (CCl4) in dioxane and acetonitrile mixtures has been studied at room temperature by steady-state fluorescence measurements. The positive deviation from linearity has been observed in the Stern-Volmer (S-V) plots for both fluorophores in different composition of mixed solvents even at moderate CCl4 concentration (0.10moldm-3). Various quenching parameters of the quenching processes have been determined using the extended S-V equation and have been found to be dependent on the solvent polarity. Further, with the use of the finite sink approximation model, it is concluded that the bimolecular quenching reactions are diffusion limited, and the distance parameter R? and mutual diffusion coefficient D are estimated independently. © Taylor & Francis Group, LLC.en_US
dc.subjectFluorescence
dc.subjectIndole
dc.subjectSolvent polarity
dc.subjectStatic and dynamic quenching
dc.subjectStern-Volmer plot
dc.titleEffect of solvent polarity on fluorescence Quenching of new indole derivatives by CCl4en_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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