Recycling of rhodium-based hydrosilylation catalysts; A fluorous approach

The concept of fluorous biphasic separation has been applied in the recycli ng of rhodium-based catalysts for the hydrosilylation of 1-alkenes and fluo rinated 1-alkenes by following two approaches. Hydrosilylation of 1-hexene using various silanes and fluorous versions of Wilkinson's catalyst [RhCl{P (C6H4-4-SiMe2Rf)(3)}(3)] (1; R-f = CH2CH2C6F13) or [RhCl{P(C6H4-4-SiMe(R-f) (2))(3)}(3)] (2; Rf = CH2CH2C8F17) in fluorous biphasic solvent systems aff orded the corresponding n-hexylsilanes in high yield. The catalyst activiti es were similar to those obtained using conventional [RhCl(PPh3)(3)]. The f luorous phase containing the catalyst was recycled at least twice without n oticeable loss of activity, despite the fact that 12 and 1.7% of [Rh] was l ost for I and 2, respectively, in the first cycle. The fluorous hydride int ermediate [Rh(H)(Cl)(SiCl3){P(C6H4-4-SiMe2Rf)(3)}(2)] (3; Rf = CH2CH2C6F13) was identified by NMR spectroscopy. In a reverse approach, the original Wi lkinson's catalyst was used for the hydrosilylation of 1H, 1H,2H-perfluoro- 1-alkenes in benzene or toluene as solvent. Fluorous extraction of the prod ucts enabled recycling of the nonfluorous catalyst.