Journal of Organometallic Chemistry p. 91 - 95 (1996)
Update date:2022-08-11
Topics:
Yeon, Seung Ho
Han, Joon Soo
Yoo, Bok Ryul
Jung, Il Nam
Direct synthesis of bis(chlorosilyl)methanes has been reinvestigated by reacting elemental silicon simultaneously with methylene chloride and hydrogen chloride in the presence of copper catalyst using a stirred reactor equipped with a spiral band agitator at a carefully controlled temperature between 260 and 340°C. Bis(dichlorosilyl)methane and (dichlorosilyl)(trichlorosilyl)methane were obtained as the major products and bis(trichlorosilyl)methane as a minor product along with trichlorosilane and tetrachlorosilane derived from the reaction between elemental silicon and hydrogen chloride. The decomposition of methylene chloride was suppressed and the production of polymeric carbosilanes reduced by adding hydrogen chloride to the methylene chloride reactant. The optimum mixing ratio of methylene chloride and hydrogen chloride for the direct synthesis of bis(silyl)methanes was 1 : 4. The deactivation problem of elemental silicon owing to decompositions of methylene chloride and polycarbosilanes was eliminated. Cadmium was a good promoter for the reaction, while zinc was found to be an inhibitor for this particular reaction.
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