New reactors and methods for the investigation of homogeneous catalysis

被引:20
作者
de Bellefon, C [1 ]
Tanchoux, N [1 ]
Caravieilhes, S [1 ]
机构
[1] CPE Lyon, Lab Genie Proc Catalyt, CNRS, URA 2211, F-69616 Villeurbanne, France
关键词
homogeneous catalysis; liquid/liquid catalysis; batch reactor; plug flow reactor; kinetics;
D O I
10.1016/S0022-328X(98)00677-9
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New methods and reactors for the kinetic investigation of homogeneous catalysis are described. These are oriented towards the minimisation of the amount of catalyst required for testing new catalytic reactions, kinetics determination and/or catalyst selection. The use of the centrifugal partition chromatograph (CPC) as a chromatographic catalytic reactor for steady-state and transient kinetics is reported. Examples are given which involve monophasic and biphasic reductions. The former is the enantioselective reduction of acetophenone to 2phenylethanol by isopropanol catalysed by a Rh/chiral diamine system. The biphasic reductions are: (i) the reduction of benzaldehyde into benzylic alcohol catalysed with a Ru/TPPTS complex and (ii) the reduction of dimethylitaconate into dimethylmethylsuccinate catalysed with a Rh/TPPTS complex, both reductions taking place in cyclohexane/water mixtures with sodium formate as the hydrogen transfer reagent. Finally, for first order reactions, analytical solutions are found which demonstrate that kinetic parameters can be readily obtained by using the CPC as a chromatographic reactor in the transient (pulse) mode. (C) 1998 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:143 / 150
页数:8
相关论文
共 17 条
[1]   RHODIUM(I)-CATALYZED BIPHASIC ISOMERIZATION OF ALLYLIC ALCOHOLS [J].
ALPER, H ;
HACHEM, K .
JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (11) :2269-2270
[2]  
[Anonymous], APPL HOMOGENEOUS CAT
[3]  
[Anonymous], APPL HOMOGENEOUS CAT
[4]  
BAERNES M, 1996, APPL HOMOGENEOUS CAT, P684
[5]   ORGANOMETALLIC CATALYSIS IN AQUEOUS-SOLUTIONS - THE BIPHASIC TRANSFER HYDROGENATION OF ALDEHYDES CATALYZED BY WATER-SOLUBLE PHOSPHINE COMPLEXES OF RUTHENIUM, RHODIUM AND IRIDIUM [J].
BENYEI, A ;
JOO, F .
JOURNAL OF MOLECULAR CATALYSIS, 1990, 58 (02) :151-163
[6]   HIGH-SPEED COUNTERCURRENT CHROMATOGRAPHY USED FOR ALKYLBENZENE LIQUID LIQUID PARTITION-COEFFICIENT DETERMINATION [J].
BERTHOD, A ;
BULLY, M .
ANALYTICAL CHEMISTRY, 1991, 63 (21) :2508-2512
[7]   INTRODUCING TPPTS AND RELATED LIGANDS FOR INDUSTRIAL BIPHASIC PROCESSES [J].
CORNILS, B ;
KUNTZ, EG .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 502 (1-2) :177-186
[8]   A liquid-liquid plug flow continuous reactor for the investigation of catalytic reactions: The centrifugal partition chromatograph [J].
de Bellefon, C ;
Caravieilhes, S ;
Joly-Vuillemin, C ;
Schweich, D ;
Berthod, A .
CHEMICAL ENGINEERING SCIENCE, 1998, 53 (01) :71-74
[9]   ASYMMETRIC CATALYTIC REDUCTION OF CARBONYL-COMPOUNDS USING C-2 SYMMETRICAL DIAMINES AS CHIRAL LIGANDS [J].
GAMEZ, P ;
FACHE, F ;
LEMAIRE, M .
TETRAHEDRON-ASYMMETRY, 1995, 6 (03) :705-718
[10]   RECENT ADVANCES IN COUNTERCURRENT CHROMATOGRAPHY [J].
ITO, Y .
JOURNAL OF CHROMATOGRAPHY, 1991, 538 (01) :3-25