Supported and Non-Supported Ruthenium(II)/Phosphine/[3-(2-Aminoethyl)aminopropyl]trimethoxysilane Complexes and Their Activities in the Chemoselective Hydrogenation of trans-4-Phenyl-3-butene-2-al

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Ismail Warad
Petrochemical Research Chair, Department of Chemistry, King Saud University, P. O. Box 2455, Riyadh 11451, Saudi Arabia
Current Affiliation: 
Department of Chemistry, Faculty of Science, An-Najah National University, Nablus, Palestine
Preferred Abstract (Original): 
Syntheses of four new ruthenium(II) complexes of the [RuCl2(P)2(N)2] type using 2-(diphenylphosphino)ethyl methyl ether (P~O) as ether-phosphine and triphenylphosphine (PPh3) as monodentate phosphine ligands in the presence of [3-(2-aminoethyl)aminopropyl]trimethoxysilane as diamine co-ligand are presented for the first time. The reactions were conducted at room temperature and under an inert atmosphere. Due to the presence of the trimethoxysilane group in the backbone of complexes 1 and 2 they were subjected to an immobilization process using the sol-gel technique in the presence of tetraethoxysilane as cross-linker. The structural behavior of the phosphine ligands in the desired complexes during synthesis were monitored by 31P{1H}-NMR. Desired complexes were deduced from elemental analyses, Infrared, FAB-MS and 1H-, 13C- and 31P-NMR spectroscopy, xerogels X1 and X2 were subjected to solid state, 13C-, 29Si- and 31P-NMR spectroscopy, Infrared and EXAF. These complexes served as hydrogenation catalysts in homogenous and heterogeneous phases, and chemoselective hydrogenation of the carbonyl function group in trans-4-phenyl-3-butene-2-al was successfully carried out under mild basic conditions.
Supported and Non-Supported Ruthenium771.32 KB