HOMOGENEOUS CATALYTIC-HYDROGENATION OF SUPERCRITICAL CARBON-DIOXIDE

被引:591
作者
JESSOP, PG [1 ]
IKARIYA, T [1 ]
NOYORI, R [1 ]
机构
[1] RES DEV CORP JAPAN, MOLEC CATALYSIS PROJECT, TOYOTA, AICHI 47003, JAPAN
关键词
D O I
10.1038/368231a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE use of carbon dioxide as a starting material for the synthesis of organic compounds has long been a goal for synthetic chemists. The hydogenation of carbon dioxide to formic acid, methanol and other organic substances is particularly attractive, but has remained difficult. This route to formic acid has been described recently, based on the use of organometallic rhodium catalysts in dimethyl sulphoxide(1) and aqueous(2) solvents. We report here the efficient production of formic acid in a supercritical mixture of carbon dioxide and hydrogen containing a catalytic ruthenium(II) phosphine complex. The use of a supercritical phase, in which hydrogen is highly miscible, leads to a very high initial rate of reaction-up to 1,400 moles of formic acid per mote of catalyst per hour. The same reaction under identical conditions but in liquid organic solvents is much slower. Our results suggest that supercritical fluids represent a promising medium for homogeneous catalysis.
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页码:231 / 233
页数:3
相关论文
共 25 条
[1]  
AALTONEN O, 1991, CHEMTECH, V21, P240
[2]  
BURGEMEISTER T, 1993, ANGEW CHEM INT EDIT, V32, P739, DOI 10.1002/anie.199307391
[3]   HOMOGENEOUS CATALYSTS FOR CARBON-DIOXIDE HYDROGEN ACTIVATION - ALKYL FORMATE PRODUCTION USING ANIONIC RUTHENIUM CARBONYL CLUSTERS AS CATALYSTS [J].
DARENSBOURG, DJ ;
OVALLES, C ;
PALA, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (18) :5937-5939
[4]  
EGGERS R, 1989, ACS SYM SER, V406, P478
[5]   CO2-ACTIVATION .3. HYDROGENATION OF CARBON-DIOXIDE TO FORMIC-ACID USING WATER-SOLUBLE RHODIUM CATALYSTS [J].
GASSNER, F ;
LEITNER, W .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1993, (19) :1465-1466
[6]   DIRECT FORMATION OF FORMIC-ACID FROM CARBON-DIOXIDE AND DIHYDROGEN USING THE [(RH(COD)CL)2]-PH2P(CH2)4PPH2 CATALYST SYSTEM [J].
GRAF, E ;
LEITNER, W .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (08) :623-624
[7]   REDUCTIVE ELIMINATION OF HYDROGEN-CHLORIDE FROM CHLORO-HYDRIDO-TRANSITION METAL-COMPLEXES - AN EFFICIENT AND SIMPLE METHOD FOR GENERATION OF ELECTRON-RICH, COORDINATIVELY UNSATURATED, REACTIVE INTERMEDIATES [J].
GRUSHIN, VV .
ACCOUNTS OF CHEMICAL RESEARCH, 1993, 26 (05) :279-286
[8]   PREPARATION AND REACTIONS OF HYDRIDOCHLOROTRIS(TRIPHENYLPHOSPHINE)-RUTHENIUM(2) INCLUDING HOMOGENEOUS CATALYTIC HYDROGENATION OF ALK-1-ENES [J].
HALLMAN, PS ;
MCGARVEY, BR ;
WILKINSON, G .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1968, (12) :3143-+
[9]   ORGANOMETALLIC PHOTOCHEMISTRY IN SUPERCRITICAL FLUIDS - THE REACTION OF H-2 WITH [(ETA-5-C5H5)RE(CO)3], [(ETA-5-C5HS)MN(CO)3] AND THE FORMATION OF A NON-CLASSICAL DIHYDROGEN COMPLEX OF MANGANESE(I) [J].
HOWDLE, SM ;
POLIAKOFF, M .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (16) :1099-1101
[10]   ORGANOMETALLIC CHEMISTRY IN SUPERCRITICAL FLUIDS - THE GENERATION AND DETECTION OF DINITROGEN AND NONCLASSICAL DIHYDROGEN COMPLEXES OF GROUP-6, 7, AND 8 TRANSITION-METALS AT ROOM-TEMPERATURE [J].
HOWDLE, SM ;
HEALY, MA ;
POLIAKOFF, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (12) :4804-4813