Add time:07/18/2019 Source:sciencedirect.com
Two ethylene-nickel(0) complexes, viz., [1,2-bis(diphenylphosphino)ethane]-(ethylene)nickel(0) and bis(triphenylphosphine)(ethylene)nickel(0) have been used in a comparison of their catalytic activities in hydrosilylation reactions with those of the corresponding nickel(II) complexes, viz., dichloro [1,2-bis(diphenylphosphino)-ethane]nickel(II) and dichlorobis(triphenylphosphine)nickel(II). The reaction profiles are similar, apart from a significant difference in the induction period; the nickel(II) catalysts requiring a substantially longer time. A mechanism involving a nickel(0) species is proposed for the hydrosilylation.The interchange of hydrogen and chlorine on silicon accompanying the hydrosilylation is related to a high electron density at the nickel atom bearing the phosphine, olefin, and silicon hydride ligands.
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