Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/20056
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dc.contributor.authorSharma, Mayur-
dc.contributor.authorJangir, Sarita-
dc.contributor.authorOjha, C K-
dc.contributor.authorPardasani, P-
dc.date.accessioned2013-07-24T10:00:28Z-
dc.date.available2013-07-24T10:00:28Z-
dc.date.issued2006-11-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/20056-
dc.description2426-2430en_US
dc.description.abstractReactions of monofunctional 9,10-phenanthrenequinone monooxime with dialkyl/diaryl-tin dichloride in desired molar ratios in refluxing benzene affords corresponding dialkyl-/diaryl-tin(IV) oximates, which have been characterized by elemental analyses (C, H, N and Sn), IR, multinuclear (1H, 13C and 119Sn) NMR and mass spectroscopy. On the basis of calculation of C-Sn-C bond angle from coupling constant, trigonal-bipyramidal and octahedral geometry are proposed for the chelates 5a-5c and 6a-6c. Semiempirical studies have been carried out to understand the tautomeric and conformational behaviour of the ligand.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt.Cl.8 C07F7/22en_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.45A(11) [November 2006]en_US
dc.titleSynthesis, spectroscopic and structural features of diorganotin(IV) oximates derived from 9,10-phenanthrenequinone monooximeen_US
dc.typeArticleen_US
Appears in Collections: IJC-A Vol.45A(11) [November 2006]

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