Abstract

The anionic ruthenium complex [Ru(CO)3Cl3]- (1) was found to catalyze the formation of methyl formate from CO2, H2, and CH3OH in the presence of a strong base. From the basic methanol solution, the dinuclear anion [Ru2(CO)4(μ2-η2-CO2CH3)2(μ2-OCH3)Cl2]- (2) has been isolated as the bis(triphenylphosphoranylidene)ammonium salt and characterized by a single-crystal X-ray diffraction analysis. In anion 2, two Ru(CO)2Cl units are held together by a μ2-OCH3 ligand and by two μ2-η2-OCOCH3 bridges; apart from the three bridging ligands there is no direct Ru−Ru interaction (distance 3.380 A). Complex 2 was found to react with 2 equiv of [OCH3]- to give two reactive intermediates 3 and 4, the latter one being considered as the catalytically active species in the hydrocondensation reaction. On the basis of the spectroscopic data and the isolation of aromatic analogues from the reaction of 2 with various phenolates, the constitution of [Ru2(CO)6(OCH3)4(μ2-OCH3)]- is proposed for the active species 4. The elimination ...

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