共查询到20条相似文献,搜索用时 6 毫秒
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The 1,2-azaphosphinine, 9 , and the 1,3-diphosphinine, 10 , can be isolated from a mixture resulting from the reaction of 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete, 1 , and ethyl isothiocyanate. The reaction of 1 with phenyl isothiocyanate yields the 1,2-azaphosphinine, 16 . Mechanisms for the formation of the compounds 9 , 10 , and 16 are suggested. The properties, the NMR, mass, and IR spectra, and the molecular and crystal structures of 9 and 10 are described and discussed. 相似文献
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Hydrolysis of 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5 -diphosphete Hydrolysis of 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5 -diphosphet ( 2 ) yields in the first step Bis(dimethylamino)phosphorylmethyliden-methyl-bis(dimethylamino)phosphorane ( 5 ). In the second step Bis(dimethylamino)phosphoryl-methyl(dimethylamino)phosphosphonylmethylen ( 6 ) is the main product of hydrolysis. In addition small amounts of methylphosphonic-bis(dimethylamide) ( 7 ) are formed. Properties, nmr and mass spectra of 5 and 6 are described, their mechanism of formation is discussed. 相似文献
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Alfred Schmidpeter Peter Mayer Johanna Stocker Kenneth A. Roberts Peter J. Stang 《Heteroatom Chemistry》1991,2(5):569-573
One example each is given for the reaction of bromoacetylenes and ethynyl-phenyliodonium tosylates with bis(diphenyl phosphino)methane. The yellow crystalline 1:1-addition products are diphospholium salts. They readily and selectively hydrolyze to give 2-phosphinoylethenyl phosphonium salts. 相似文献
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The reactions of bromophenylacetylene with the diphenylphosphino amines (Ph2P)2NH and (Ph2P)3N result in the 1,1,3,3,4-pentaphenyl-1,2,5-azadiphospholium bromide ( 5 ) and its 4-diphenylphosphino derivative ( 7 ). Their X-ray structure analyses show planar rings for the cations. The small endocyclic angle at the nitrogen ring member is associated with PN bonds that are longer than in the acyclic cation (Ph3P)2N+. The data fit to a negative linear relationship of PN bond lengths and PNP bond angles. © 1997 John Wiley & Sons, Inc. 相似文献
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Klaus Bieger Gernot Heckmann Ekkehard Fluck Frank Weller Karl Peters Eva-Maria Peters 《无机化学与普通化学杂志》1995,621(12):1981-1988
1,4-Dihydro-1λ5,4λ5-[1,4]diphosphinines and a 1,4-Dihydro-1λ3,4λ3-[1,4]diphosphinine Reaction of thio- or dithiocarbonic acids with ethinyl amino phosphanes leads to 1,4-dihydro-1λ5,4λ5-[1,4]diphosphinine-1,4-disulfides. By this route compounds 4, 7 , and 8 have been prepared. Desulfurization of 4 with tri-n-butylphosphane results in 1,2,4,5-tetraphenyl-1,4-dihydro-1λ3,4λ3-[1,4]-diphosphinine 5 , which can be oxidized with tert-butyl-peroxide to the corresponding dioxide, 6 . From the reaction mixture of phenyl-phenylethinyl diethylamino phosphane and thioacetamide compound 4 and the unsymmetrical 1,4-dihydro-1λ5,4λ5-[1,4]diphosphinine 9 were isolated. Properties, nmr, ir and mass spectra of all new products are reported. A mechanism for the formation of 9 is suggested. The results of the X-ray structure determination of 8 and 9 are described. 相似文献