The rate of hydrolysis-condensation reaction of phenyltrichlorosilane in water-acetone solutions and the product yields were shown to significantly depend on the concentration of HCl (C) in the solutions. The main product of the reaction was all-(tetrahydroxy)(tetraphenyl)cyclotetrasiloxane. This was different from the earlier published results of analogous reactions of -tolylSiCl, -ClPhSiCl, and -naphtylSiCl, in which some products of other types were formed.
View Article and Find Full Text PDFThe hydrolysis-condensation reactions of -tolyl, -chlorophenyl, and -naphtyl-trichlorsilanes, (, , and , respectively) in water-acetone solutions were examined for how they were influenced by the change in the concentration of HCl (C). The composition of the products was monitored by Si NMR spectroscopy and atmospheric pressure chemical ionization mass spectrometry (APCI-MS). The acidity of the medium was shown to affect the yields of the products, and so, what products were formed.
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