Dinuclear and tetranuclear cages of oxodiphenylantimony phosphinates: Synthesis and structures

dc.contributor.author Said, Musa A.
dc.contributor.author Kumara Swamy, K. C.
dc.contributor.author Poojary, Damodara M.
dc.contributor.author Clearfeld, Abraham
dc.contributor.author Veith, M.
dc.contributor.author Huch, V.
dc.date.accessioned 2022-03-27T09:58:10Z
dc.date.available 2022-03-27T09:58:10Z
dc.date.issued 1996-01-01
dc.description.abstract The novel dimeric compounds [Ph2Sb(O2PR2)O]2·2CH 2Cl2 [R - cycl-C6H11 (2) and cycl-C8H15 (3)] have been synthesized by reacting diphenylantimony trichloride (1) with 3 mol equiv of silver acetate followed by 1 mol equiv of the phosphinic acid. By the same route under more stringent conditions to exclude moisture, the mixed phosphinate-acetate [Ph2Sb(O2Sb(O2P(C6H 11)2)(O2CMe)]2O (4) was isolated and characterized. Treatment of 2 with acetic acid/water affords the tetranuclear cage Ph8Sb4O4(OH)2(O2P(C 6H11)2)2·CH 3COOH·CH2Cl2 (5); it is possible to convert 5 to 2 by heating it with an excess of the phosphinic acid. Compounds 2, 3, and 5 have been characterized by X-ray structural analysis. All of them possess four membered Sb2O2 rings with hexacoordinated antimony. In 5 the antimony atoms in the two Sb2O2 rings are connected by oxo bridges on two sides to give an Sb4O6 cage. These structures are correlated with those of known tin cages.
dc.identifier.citation Inorganic Chemistry. v.35(11)
dc.identifier.issn 00201669
dc.identifier.uri 10.1021/ic950713w
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ic950713w
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13484
dc.title Dinuclear and tetranuclear cages of oxodiphenylantimony phosphinates: Synthesis and structures
dc.type Journal. Article
dspace.entity.type
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