1,1,3,3,5,5,7,7-octaphenyl-1,3,5,7-tetrasiloxane-1,7-diol and its organotin derivatives.: Model compounds for diphenylsiloxane polymer

被引:20
作者
Beckmann, J
Jurkschat, K [1 ]
Müller, D
Rabe, S
Schürmann, M
机构
[1] Univ Dortmund, Fachbereich Chem, Lehrstuhl Anorgan Chem 2, D-44221 Dortmund, Germany
[2] Inst Angew Chem, D-12484 Berlin, Germany
关键词
D O I
10.1021/om990107z
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The hydrolysis of the spirotitanasiloxane Ti[(OSiPh2)(4)O](2) provides 1,1,3,3,5,5,7,7-octaphenyl-1,3,5,7-tetrasiloxane-1,7-diol, H(OSiPh2)(4)OH (1), in high yield. The reaction of 1 with tricyclohexyltin hydroxide, cyclo-Hex(3)SnOH, and di-tert-butyltin oxide, cyclo-(t-Bu2SnO)(3), respectively, gives 1,1,3,3,5,5,7,7-octaphenyl-1,7-tricyclohexylstannyl-1,3,5,7-tetrasiloxane (cyclo-Hex(3)SnOSiPh(2)OSiPh(2))(2)O (2), and 1,1-di-tert-(butyl-3,5,7,9-octaphenyl-2, 4,6,8,10-pentaoxa-,3,5,7,9-tetrasila-1-stannacyclododecane, cyclo-t-Bu2Sn(OSiPh2OSiPh2)(2)O (3). The molecular structures of 1 and 2 were determined by X-ray diffraction. In both compounds the central Si-O-Si angle amounts to 180 degrees. Remarkably, no hydrogen bonding is observed for 1.
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页码:2326 / 2330
页数:5
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