TY - JOUR
T1 - Some insights into the preparation of Pt/γ-Al2O3 catalysts for the enantioselective hydrogenation of α-ketoesters
AU - Li, Xiaohong
AU - You, Xin
AU - Ying, Pinliang
AU - Xiao, Jianliang
AU - Li, Can
PY - 2003/11
Y1 - 2003/11
N2 - Pt/γ-Al2O3 catalysts were prepared by two different impregnation methods and characterized by XRD, TEM, and CO chemisorption. The Pt particle sizes ranged in 2.4-23.3 nm for these Pt-γ-Al2O3 catalysts. CO was used as a probe molecule. Due to the interaction of platinum precursor with γ-Al2O3, induced particularly after the calcination at high temperature, the Pt/γ-Al2O3 catalysts prepared by impregnation, calcination, and reduction in a sodium formate solution exhibited higher activities for both the enantioselective hydrogenations of ethyl pyruvate and ethyl 2-oxo-4-phenylbutyrate. The Pt/γ-Al2O3 catalysts, prepared by impregnation in a solution containing isopropanol without drying or calcination, did not show high catalytic performance in the enantioselective hydrogenation of ethyl pyruvate because the surface properties after the addition of isopropanol are not beneficial to the adsorption of reactant, solvent, and chiral modifier, or because the residual isopropanol blocked the adsorption of reactant, solvent, and chiral modifier.
AB - Pt/γ-Al2O3 catalysts were prepared by two different impregnation methods and characterized by XRD, TEM, and CO chemisorption. The Pt particle sizes ranged in 2.4-23.3 nm for these Pt-γ-Al2O3 catalysts. CO was used as a probe molecule. Due to the interaction of platinum precursor with γ-Al2O3, induced particularly after the calcination at high temperature, the Pt/γ-Al2O3 catalysts prepared by impregnation, calcination, and reduction in a sodium formate solution exhibited higher activities for both the enantioselective hydrogenations of ethyl pyruvate and ethyl 2-oxo-4-phenylbutyrate. The Pt/γ-Al2O3 catalysts, prepared by impregnation in a solution containing isopropanol without drying or calcination, did not show high catalytic performance in the enantioselective hydrogenation of ethyl pyruvate because the surface properties after the addition of isopropanol are not beneficial to the adsorption of reactant, solvent, and chiral modifier, or because the residual isopropanol blocked the adsorption of reactant, solvent, and chiral modifier.
KW - CO adsorption
KW - Cinchonidine
KW - EOPB
KW - Enantioselective hydrogenation
KW - Ethyl pyruvate
KW - FT-IR spectroscopy
KW - Pt/γ-AlO
UR - https://www.scopus.com/pages/publications/0347534765
U2 - 10.1023/B:TOCA.0000003098.58993.cd
DO - 10.1023/B:TOCA.0000003098.58993.cd
M3 - 文章
AN - SCOPUS:0347534765
SN - 1022-5528
VL - 25
SP - 63
EP - 70
JO - Topics in Catalysis
JF - Topics in Catalysis
IS - 1-4
ER -