Abstract

The air- and moisture-insensitive half-sandwich complexes [(η5-Cp*)Rh(L)Cl][PF6] (1–3) and [(η5-Cp*)Ir(L)Cl][PF6] (4–6) have been prepared by reacting L = L1–L3 (1,2-bis(phenylthio)ethane (L1), 1-(phenylseleno)-2-(phenylthio)ethane (L2) and 1,2-bis(phenylseleno)ethane (L3)) with [(η5-Cp*)RhCl(μ-Cl)]2 and [(η5-Cp*)IrCl(μ-Cl)]2, respectively, at room temperature followed by treatment with NH4PF6. Their HR-MS and 1H, 13C{1H}, and 77Se{1H} NMR spectra have authenticated them. The single-crystal structures of 1–6 have been established by X-ray crystallography. Complexes 1–6 have been explored for catalytic Oppenauer-type oxidation of alcohols and transfer hydrogenation of ketones with 2-propanol. 3 and 6 were the most efficient in the two catalytic reactions (TON values up to 9.9 × 102 and 9.8 × 103, respectively) and were therefore investigated in detail. 3 is the first example of a Rh(III) species explored for Oppenauer-type oxidation. The catalysis appears to be homogeneous. In transfer hydrogenation it app...

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