Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/41754
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dc.contributor.authorPrasad, B V-
dc.contributor.authorKaur, D-
dc.contributor.authorUppal, P-
dc.date.accessioned2017-05-12T09:13:29Z-
dc.date.available2017-05-12T09:13:29Z-
dc.date.issued1997-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41754-
dc.description1013-1017en_US
dc.description.abstractAb initio calculations show that silylenes can show lewis acidic behaviour. The complexation between silylenes and lewis bases proceeds without energy barrier. The resultant silylene-lewis base complexes show nucleophilicity. The larger the stabilization between silylene and lewis base, the larger is the nucleophilicity of the resultant complex. Silylenes can show nucleophilicity only after their electrophilicity gets satisfied.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.36A(12) [December 1997]en_US
dc.titleDo silylenes show ambiphilicity?:A theoretical studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.36A(12) [December 1997]

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