239478-65-0Relevant academic research and scientific papers
Trichlorosilylation of chlorogermanes and chlorostannanes with HSiCl3/Net3 followed by base-catalysed formation of (Me3Ge)2Si(SiCl3)2 and related branched stannylsilanes
Mueller, Lars,Du Mont, Wolf-Walther,Ruthe, Frank,Jones, Peter G.,Marsmann, Heinrich C.
, p. 156 - 163 (2007/10/03)
Chlorotrimethylgermane 1 and dichlorodimethylgermane 4 react with trichlorosilane and triethylamine to provide trichlorosilylgermanes Me4-nGe(SiCl3)n (n = 1: 2; n = 2: 5) in fair yields, as distillable liquids. The formation of 2 is followed by base-catalysed decomposition reactions leading to novel solid (Me3Ge)2Si(SiCl3)2 3. Chlorotrialkylstannanes 6a-c (6a: R = CH3, 6b: R = C2H5, 6c: R = n-C4H9) react with trichlorosilane and triethylamine providing the branched silylstannanes (R3Sn)2Si(SiCl3)2 7a-c and traces of silylstannanes R3SnSiCl3 8a-c. Only 7a was isolated in a pure state. Heating 7a or crude 7b and 7c with benzyl chloride leads to the formation of benzyltrichlorosilane (10). The constitution of compounds 2, 3, 5 and 7a was confirmed by MS, NMR and analytical data. The structures of C6D6-solvated 3 and C6H6-solvated 7a were determined by X-ray diffraction, and shown to be isotypic.
Intermediates and products of the hexachlorodisilane cleavage of group 14 element phosphanes and amines - Molecular structure of di-tert- butyl(trichlorosilyl)phosphane in the gas phase determined by electron diffraction and ab Initio calculations
Du Mont, Wolf-W.,Müller, Lars,Martens, Reiner,Papathomas, Paul M.,Smart, Bruce A.,Robertson, Heather E.,Rankin, David W. H.
, p. 1381 - 1392 (2007/10/03)
Reactions of dialkyl(trimethylsilyl)phosphanes RR'PSiMe3 (1: R, R' = tBu; 3: R, R' = iPr; 5: R = iPr, R' = tBu) with Si2Cl6 provide stable trichlorosilylphosphanes RR'PSiCl3 (2, 4, 6); the reactions of silyl- and stannylamines of iPr2NMMe3 (M = Si: 11; M = Sn: 12) with Si2Cl6, however, provide the stable pentachlorodisilanylamine iPr2NSi2Cl5 (13). Heating of 1 with the technical mixture Me2(Cl)SiSiCl2Me/(MeCl2Si)2 yields the stable silylphosphane tBu2PSiMe2Cl (8) and the disilanylphosphane tBu2PSi(Me)(Cl)Si(Me)Cl2 (9). Methylation of 9 with MeLi gave tBu2PSi2Me5 10, which was isolated in a pure state. Reactions of tBu(iPr)PSiMe3 (5) and of organometal phosphanes tBu(iPr)PMR3 (14: M = Ge, R = Me; 17a-c: M = Sn; R = Me, Et, nBu) with Si2Cl6 were monitored by 31P, 29Si, and 119Sn NMR. - In the first step of these reactions, new tBu(iPr)PSi2Cl5 (7) is formed. 7 is accompanied by increasing amounts of tBu(iPr)PSiCl3 (6) and Me3GeSiCl3 (15)/(Me3Ge)2Si(SiCl3)2 (16) or traces of compounds R3SnSiCl3 (19a-c) that decompose providing (R3Sn)2Si(SiCl3)2 (18a-c) and nBu3SnSi(SiCl3)3 (20c). Subsequently, compounds 19a-c decompose providing increasing amounts of 18a-c. Stannylphosphane 17b is also cleaved by SiCl4 leading to 6 with liberation of Et3SnCl, whereas 17b is formed from the reaction of 5 with Et3SnCl under liberation of Me3SiCl. The suggestion of an extra stabilisation of P-Si bonds of trichlorosilylphosphanes was subjected to direct evidence through the structure determination of the trichlorosilylphosphane tBu2PSiCl3 (2) in the gas phase by electron diffraction. This crowded molecule has a 'normal' P-Si bond length of 225.0(12) pm; its C1 symmetric conformation with both tBu groups and the SiCl3 group twisted about 17°from the perfectly staggered positions, and with each of the three groups tilted about 6°away from each other, allows to reduce steric strain.
