Abstract
The novel trans-[RuCl2(dpme)(L)] complexes (1L(1)-1L(4)) {dpme is H2C=C(CH2PPh2)(2) and L is 1,2-ethanediamine (L-1), 1,3-propanediamine (L-2), 2,2-dimethyl-1,3-propanediamine (L-3) and 1,4-butanediamine (L-4)} were obtained by reacting trans-[RuCl2(dpme)(2)] with an excess amount of the corresponding diamine in CH2Cl2 as the solvent. One of the diphosphine ligands was quantitatively replaced by the corresponding diamine, even when excess diamine was added. In solution the trans-[RuCl2(dpme)(diamine)] isomer configuration was confirmed by NMR spectroscopy and the X-ray crystal structure of 1L(2) was also determined. These diphosphine complexes (1L(1)-1L(4)) have exhibited significant activity and selectivity as hydrogenation catalysts for alpha,beta-unsaturated ketones. Increasing the chelating ring of the diamine ligands from five and six to seven decreases the turnover frequencies (TOFs). The catalytic activities were compared to the analogous trans-[RuCl2(dppp)(L)] (2L(1)-2L(4)) {dPPP is H2C(CH2PPh2)(2)}. Complexes 1L(1)-1L.(4) catalyzed the hydrogenation of alpha,beta-unsaturated ketones faster than the previously reported complexes 2L(1)-2L(4) Density functional theory (DFT) calculations have been carried out to study the shift in the Ru(III)/Ru(II) couple and the catalytic activity for two representative complexes, 1L(2) and 2L(2). (C) 2013 Elsevier Ltd. All rights reserved.