Isomerization of olefins by phosphine-substituted ruthenium complexes and influence of an ‘additional gas’ on the reaction rate

Abstract

Phosphine-substituted ruthenium carbonyls have often been used as catalytic precursors in reactions such as the hydrogenation or the hydroformylation of olefins. To collect evidence on the coordination of the olefin as a preliminary step of these reactions we have investigated the isomerization of hex-1-ene, in hydrocarbon solvent, in the presence of the phosphine-substituted ruthenium carbonyls Ru(CO) 3(PR 3) 2, Ru 3(CO) 9(PR 3) 3 and Ru(CO) 2(OAc) 2(PR 3) 2 [R=Bu, Ph]. When using Ru(CO) 3(PPh 3) 2 the rate of the reaction shows a partial first order with respect to the concentration of the catalyst and of the substrate. The activation parameters were also evaluated and the activation entropy is negative. A reaction scheme involving the displacement of a carbonyl ligand with formation of a π-olefin–ruthenium complex is suggested. The rate of the reaction significantly changes if an alcohol is used as solvent. This behaviour is attributed to a modification of the catalytic precursor with formation of a ruthenium hydride. This hypothesis is confirmed by the identification of an alkoxy ruthenium hydride. The isomerization of olefins by phosphine-substituted ruthenium carbonyls is retarded by the presence of an ‘additional gas’ such as dinitrogen. This influence is more evident than the analogous one reported in the hydroformylation reaction: the same pressure of the ‘additional gas’ present in the reaction vessel reduces the rate of the isomerization to a larger extent, i.e. the presence of 1000 bar of nitrogen decreases in otherwise identical experiments the isomerization conversion of hex-1-ene from 95.6% to 25.8%. An analogous effect is also caused by the presence of argon and xenon. Helium, on the other hand, does not display any influence. These data are an indication of an interaction between the ‘additional gas’ and a catalytically active transition metal complex.