Tetraphenylantimony(V) O,O′-dialkyl dithiophosphates [Sb(C6H5)4{S2P(OR)2}] (R = s-C4H9, c-C6H11): Synthesis, structures, and 13C and 31P CP/MAS NMR spectra

被引:0
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作者
M. A. Ivanov
V. V. Sharutin
A. V. Ivanov
A. V. Gerasimenko
O. N. Antsutkin
机构
[1] Russian Academy of Sciences,Institute of Geology and Nature Management, Amur Scientific Center, Far East Division
[2] Blagoveshchensk State Pedagogical University,Institute of Chemistry, Far East Division
[3] Russian Academy of Sciences,undefined
[4] Luleå University of Technology,undefined
来源
Russian Journal of Coordination Chemistry | 2008年 / 34卷
关键词
Coordination Chemistry; Trigonal Bipyramid; Bidentate Coordination; Antimonite; Chemical Shift Tensor;
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摘要
Tetraphenylantimony(V) O,O′-di-sec-butyl dithiophosphate (I) and tetraphenylantimony(V) O,O′-dicyclohexyl dithiophosphate (II) [Sb(C6H5)4{S2P(OR)2}] (R = sec-C4H9 or cyclo-C6H11) were obtained. Their structures and spectroscopic properties were studied by X-ray diffraction analysis and 13C and 31P CP/MAS NMR spectroscopy. The dithiophosphate (Dtph) ligands in complexes I and II were found to be coordinated in S-monodentate and S,S′-bidentate fashions, respectively (MAS NMR data). According to X-ray diffraction data, the coordination polyhedron of antimony in molecular structure I is a trigonal bipyramid with unusual monodentate coordination of the Dtph group in the axial position.
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页码:527 / 535
页数:8
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