Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/41167
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dc.contributor.authorSidhu, M S-
dc.contributor.authorBhatia, P V K-
dc.contributor.authorKapila, Vandana-
dc.date.accessioned2017-04-07T09:19:08Z-
dc.date.available2017-04-07T09:19:08Z-
dc.date.issued1994-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41167-
dc.description1093-1095en_US
dc.description.abstractElectron absorption spectroscopy has been used to measure bimolecular photophysical deactivation constant by exploiting photochemical reduction of uranyl ion with triphenylphosphine. Relative rates of bimolecular quenching follow the order SCN- > Cl- > CCl4 > CHCl3 > CH2Cl2 showing that free ionic halide and increasing number of chlorine atoms in covalently bonded alkyl halides increase the bimolecular quenching action. The increased availability of non-bonding electrons on halogen atom facilitate interaction with electron deficient species (excited uranyl ion).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.33A(12) [December 1994]en_US
dc.titleQuenching of excited uranyl ion during its photochemical reduction by triphenylphosphine: Part V-Effect of covalently bonded and ionic halidesen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.33A(12) [December 1994]

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