Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46909
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dc.contributor.authorDatta, K K-
dc.contributor.authorMukherjee, A K-
dc.date.accessioned2019-03-28T06:27:01Z-
dc.date.available2019-03-28T06:27:01Z-
dc.date.issued1989-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46909-
dc.description1025-1028en_US
dc.description.abstractThe systematic red shift of the charge transfer (CT) absorption maxima of π-molecular complexes of tetracyanoethylene with furan and thiophene by t-butyl substitution at 2- and 3-positions of the donors has been utilised to get the inductive effect PMO parameter of t-butyl group. The HOMOs of furan and thiophene have been calculated by HMO method and those of the 2- and 3-t-butyl substituted derivatives have been obtained as a function of the PMO parameter (ht) of the t-butyl group by applying Coulson-Longuet-Higgins perturbation method. The value of ht is found to be -0.516, a value which is somewhat higher, as expected, than the PMO parameter for methyl group reported earlier for π -molecular complexes of methylated electron donors. Thiophene MOs have been calculated by two models and one of them, proposed by Longuet-Higgins, has been shown to be more reliable.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.28A(12) [December 1989]en_US
dc.titleEstimation of inductive effect PMO-parameter of t-butyl group from charge transfer bands of some π-molecular complexes of furan and thiophene derivativesen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(12) [December 1989]

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