RimoldiPresent address: Department of Chemistry, M., University, Northwestern, Road, 2145 Sheridan, Evanst, Fodor, D., van Bokhoven, J. A., and Mezzetti, A.
The previously reported silica-grafted iridium(iii) hydride complex [IrH(O–SBA-15)(POCOP)] (2), prepared by treating [IrH2(POCOP)] (1) (POCOP is 1,3-bis((di-tert-butylphosphino)oxy)benzene) with SBA-15 (mesoporous silica), hydrogenates liquid alkenes (1-decene, trans-5-decene, cyclohexene, styrene, and 4-phenyl-1-butene) at room temperature and under 1 atm H2. Internal alkenes react at a lower rate than the terminal ones. For the sake of comparison, the hydrogenation of the same substrates was studied with the homogeneous catalyst [IrH2(POCOP)] (1). The heterogeneous catalyst 2hydrogenates 1-decene, cyclohexene, and 4-phenyl-1-butene faster than 1, whereas the opposite is true for styrene and trans-5-decene, which suggests that different active species are involved in the heterogeneous and homogeneous reactions. Catalysis by a truly heterogeneous species is supported by a series of “hot filtration tests”. NMR spectroscopic studies showed that 2does not undergo degrafting upon longer exposure to alkenes compared to ethene under hydrogenation conditions.