作者:A. G. Shipov、E. P. Kramarova、T. P. Murasheva、A. A. Korlyukov、S. A. Pogozhikh、S. A. Tarasenko、V. V. Negrebetskii、I. P. Yakovlev、Yu. I. Baukov
DOI:10.1134/s1070363211120048
日期:2011.12
Hydrolysis of monochelate five-coordinate chlorosilanes MeC(O)N(Me)CH2SiMe2Cl (Ia), (LCH2SiMe2Cl)-C-7 (Ib), (LCH2SiMe2Cl)-C-8 (Ic), PhtImCH(2)SiMe(2)Cl (Id), MeC(O)N(Me)CH2SiMePhCl (IIa), and Im(5)CH(2)SiMePhCl (IIe), containing a monoanionic C,O-chelating ligand LCH2 [L is an amide, n-membered lactam (L (n) ), imide (Im (n) ), or phthalimide (PhtIm) residue]. The structures of the starting chlorides and their hydrolysis products were established by means of X-ray diffraction analysis. Based on experimental and published data, a general scheme of hydrolysis of mono-C,O-chelate chlorosilanes was suggested, including initial formation of silyloxonium chlorides III and subsequent formation of disiloxane dihydrochlorides IV.