Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40099
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dc.contributor.authorRandhawa, H S-
dc.contributor.authorJassal, M S-
dc.contributor.authorSirdhana, B-
dc.contributor.authorSekhon, B S-
dc.date.accessioned2017-02-06T04:43:16Z-
dc.date.available2017-02-06T04:43:16Z-
dc.date.issued1998-06-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40099-
dc.description517-520en_US
dc.description.abstractElectronic absorption and electron spin resonance spectroscopic measurements have been made on the interaction between uracil, 2- thiouracil, 5-substituted uracils and 2' -deoxyuridine as <i>n</i>-donors and chloranil as π-acceptor. The studies reveal that EDA complex of charge transfer type acts as precursor to the formation of uraci/uridinium free diradical canon and trichlorohydroxyquinone. The electronic absorption bands in the 615-625 nm range are attributed to red coloured trichlorohydroxyquinone while ESR signal is assigned to free diradical cation. The thermodynamic stability constants, K, for the various D-A systems, as determined from the Benesi-Hildebrand model, follow the ascending order, 5-methyluracil < 5- arninouracil <Uracil <5-iodouracil <2-thiouracil < 5- bromouracil < 5-nitrouracil.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.37A(06) [June 1998]en_US
dc.titleSpectroscopic studies of molecular interactions involving 5- substituted uracil donors and chloranil as an electron acceptoren_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.37A(06) [June 1998]

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