18546-93-5Relevant articles and documents
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Bank,H.M. et al.
, p. 792 - 794 (1964)
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Olefin isomerization and hydrosilylation catalysis by lewis acidic organofluorophosphonium salts
Perez, Manuel,Hounjet, Lindsay J.,Caputo, Christopher B.,Dobrovetsky, Roman,Stephan, Douglas W.
supporting information, p. 18308 - 18310 (2014/01/06)
Organofluorophosphonium salts of the formula [(C6F 5)3-xPhxPF][B(C6F5) 4] (x = 0, 1) exhibit Lewis acidity derived from a low-lying σ* orbital at P opposite F. This acidity is evidenced by the reactions of these salts with olefins, which catalyze the rapid isomerization of 1-hexene to 2-hexene, the cationic polymerization of isobutylene, and the Friedel-Crafts-type dimerization of 1,1-diphenylethylene. In the presence of hydrosilanes, olefins and alkynes undergo efficient hydrosilylation catalysis to the alkylsilanes. Experimental and computational considerations of the mechanism are consistent with the sequential activation and 1,2-addition of hydrosilane across the unsaturated C-C bonds.