TY - JOUR
T1 - Crucial parameters in the selective biphasic hydrogenation of cinnamaldehyde by biphasic Ru-TPPTS and Ru-(TPPTS)3 catalysts
AU - Nuithitikul, Kamchai
AU - Winterbottom, John
PY - 2007/10/15
Y1 - 2007/10/15
N2 - A number of important features in the selective hydrogenation of CALD by biphasic Ru-TPPTS catalysts (TPPTS = tris(m-sulfonatophenyl) phosphine trisodium salt) are discussed. These include the methods of synthesis of water-soluble Ru-TPPTS catalysts, the influence of pH during the synthesis and the hydrogenation reaction conditions (the concentration of catalysts, excess amounts of TPPTS, mass transfer characteristics). The Ru-TPPTS catalyst is not only selective at C=O bonds (which is generally known) but also at C=C bonds if certain parameters are controlled carefully. Ninety-six percentage selectivity to unsaturated alcohol and 97% selectivity to saturated aldehyde were achieved under optimum conditions. Some characteristics of the biphasic hydrogenation by RhCI(TPPTS)3 catalyst are also mentioned and compared, particularly those promoting the high selectivity to saturated aldehyde. (C) 2007 Elsevier B.V. All rights reserved.
AB - A number of important features in the selective hydrogenation of CALD by biphasic Ru-TPPTS catalysts (TPPTS = tris(m-sulfonatophenyl) phosphine trisodium salt) are discussed. These include the methods of synthesis of water-soluble Ru-TPPTS catalysts, the influence of pH during the synthesis and the hydrogenation reaction conditions (the concentration of catalysts, excess amounts of TPPTS, mass transfer characteristics). The Ru-TPPTS catalyst is not only selective at C=O bonds (which is generally known) but also at C=C bonds if certain parameters are controlled carefully. Ninety-six percentage selectivity to unsaturated alcohol and 97% selectivity to saturated aldehyde were achieved under optimum conditions. Some characteristics of the biphasic hydrogenation by RhCI(TPPTS)3 catalyst are also mentioned and compared, particularly those promoting the high selectivity to saturated aldehyde. (C) 2007 Elsevier B.V. All rights reserved.
U2 - 10.1016/j.cattod.2007.05.019
DO - 10.1016/j.cattod.2007.05.019
M3 - Article
SN - 0920-5861
VL - 128
SP - 74
EP - 79
JO - Catalysis Today
JF - Catalysis Today
IS - 1-2
ER -