18410-59-8Relevant articles and documents
Nickel catalyzed Coupling of Phenylhydrosilanes
Boudjouk, Philip,Rajkumar, Amirthini B.,Parker, W. L.
, p. 245 - 246 (1991)
Activated nickel, prepared by lithium reduction of nickel iodide in tetrahydrofuran, catalyses the dehydrogenative coupling of phenylsilanes to form di-, tri-, and tetrasilanes.
Reactivity of group 4 benzamidinate complexes towards mono- and bis-substituted silanes and 1,5-hexadiene
Volkis, Victoria,Averbuj, Claudia,Eisen, Moris S.
, p. 1940 - 1950 (2007/10/03)
Zirconium and titanium bis(benzamidinate) dimethyl complexes were found to be active catalytic precursors for the oligomerization of mono- and bis-substituted silanes. The activation of such complexes, by an excess of MAO or by an equimolar amount of B(C
Electrochemical synthesis of symmetrical difunctional disilanes as precursors for organofunctional silanes
Grogger, Christa,Loidl, Bernhard,Stueger, Harald,Kammel, Thomas,Pachaly, Bernd
, p. 105 - 110 (2007/10/03)
Difunctional disilanes of the general type XR2SiSiR2X (1-5) (X = OMe, H; R = Me, Ph, H) have been synthesized by electrolysis of the appropriate chlorosilanes XR2SiCl in an undivided cell with a constant current supply and in the absence of any complexing agent. Reduction potentials of the chlorosilane starting materials derived from cyclic voltammetry measurements were used to rationalize the results of preparative electrolyses. Organofunctional silanes of the general formula MeO(Me 2)SiC6H4Y (6a-c, 7) were subsequently obtained by the reaction of sym-dimethoxytetramethyldisilane (1) with NaOMe in the presence of p-functional aryl bromides BrC6H4Y (Y = OMe, NEt2, NH2).