The regioselective biphasic hydrogenation of trans-cinnaldehyde by meta sulfonatophenyl-diphenylphosphine (TPPMS) Ru(II) and Os(II) species. The influence of ionic strength, ligand tensoactivity and metal nature in the selective production of the unsaturated alcohol
F. Lopez-linares et al., The regioselective biphasic hydrogenation of trans-cinnaldehyde by meta sulfonatophenyl-diphenylphosphine (TPPMS) Ru(II) and Os(II) species. The influence of ionic strength, ligand tensoactivity and metal nature in the selective production of the unsaturated alcohol, J MOL CAT A, 145(1-2), 1999, pp. 61-68
The hydrogenation of trans-cinnamaldehyde was studied, using as catalyst pr
ecursor the complexes MCl2(CH3CN)(4), where M = Ru(II) and Os(II), stabiliz
ed with the water-soluble ligand, meta-sulfonatophenyl-diphenylphosphine in
its sodium salt form, (TPPMS). The Ru(II) system showed better activity an
d selectivity than its Os(II) analogue, under biphasic catalysis. For the r
uthenium system an enhancement of the selectivity to the unsaturated alcoho
l was obtained by increasing substrate to catalyst ratio, salt concentratio
n and ligand tensoactivity. (C) 1999 Elsevier Science B.V. All rights reser
ved.