Scope and limitation of activated carbons in aqueous organometallic catalysis

被引:12
作者
Kania, Nicolas [1 ,2 ,4 ]
Gokulakrishnan, Narasimhan [1 ,2 ,4 ]
Leger, Bastien [1 ,2 ,4 ]
Fourmentin, Sophie [1 ,3 ]
Monflier, Eric [1 ,2 ,4 ]
Ponchel, Anne [1 ,2 ,4 ]
机构
[1] Univ Lille Nord France, F-59000 Lille, France
[2] UArtois, UCCS, F-62300 Lens, France
[3] ULCO, UCEIV, EA 4492, F-59140 Dunkerque, France
[4] CNRS, UMR 8181, F-75700 Paris, France
关键词
Mass transfer; Activated carbons; Palladium; Phosphanes; TPPTS; Tsuji-Trost reaction; Biphasic catalysis; Sustainable chemistry; RHODIUM HYDROFORMYLATION CATALYSTS; BIPHASIC HYDROFORMYLATION; 2-PHASE HYDROFORMYLATION; PALLADIUM COMPLEXES; SURFACE-PROPERTIES; PHASE CATALYSIS; MASS-TRANSFER; WATER; ADSORPTION; EFFICIENT;
D O I
10.1016/j.jcat.2010.12.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The effect of activated carbons has been studied in the palladium-catalyzed cleavage reaction of allylalkylcarbonate under aqueous biphasic conditions. A number of parameters were investigated, such as the type of carbon, the structure of the water-soluble ligand, the water conditions, and the metal complex loading. It was found that the intrinsic properties of carbons had a strong influence on the reaction rates. The best performances were obtained with the AC-WV carbon possessing the largest part of mesopores and lowest content of oxygen-surface groups. The results were rationalized by considering that AC-WV acted as a mass-transfer promoter increasing the interfacial area and collisions between the reactive species in the pore volume. The hypothesis of a confinement effect of the catalyst and reactants within the pores via adsorption-desorption processes was supported by isothermal studies and P-31{H-1} NMR investigations. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:208 / 218
页数:11
相关论文
共 50 条
[21]   Hydroformylation of long-chain alkenes with new supported aqueous phase catalysts [J].
Disser, C ;
Muennich, C ;
Luft, G .
APPLIED CATALYSIS A-GENERAL, 2005, 296 (02) :201-208
[22]   Supported aqueous-phase palladium catalysts for the reaction of allylic substitution: Toward an understanding of the catalytic system [J].
dos Santos, S ;
Tong, YY ;
Quignard, F ;
Choplin, A ;
Sinou, D ;
Dutasta, JP .
ORGANOMETALLICS, 1998, 17 (01) :78-89
[23]   Influence of HNO3 oxidation on the structure and adsorptive properties of corncob-based activated carbon [J].
El-Hendawy, ANA .
CARBON, 2003, 41 (04) :713-722
[24]   SELECTIVE HYDROGENATION OF ALPHA,BETA-UNSATURATED ALDEHYDES CATALYZED BY SUPPORTED AQUEOUS-PHASE CATALYSTS AND SUPPORTED HOMOGENEOUS CATALYSTS [J].
FACHE, E ;
MERCIER, C ;
PAGNIER, N ;
DESPEYROUX, B ;
PANSTER, P .
JOURNAL OF MOLECULAR CATALYSIS, 1993, 79 (1-3) :117-131
[25]   A Property-Matched Water-Soluble Analogue of the Benchmark Ligand PPh3 [J].
Ferreira, Michel ;
Bricout, Herve ;
Hapiot, Frederic ;
Sayede, Adlane ;
Tilloy, Sebastien ;
Monflier, Eric .
CHEMSUSCHEM, 2008, 1 (07) :631-636
[26]   Expanded scope of supported aqueous phase catalysis: Efficient rhodium-catalyzed hydroformylation of alpha,beta-unsaturated esters [J].
Fremy, G ;
Monflier, E ;
Carpentier, JF ;
Castanet, Y ;
Mortreux, A .
JOURNAL OF CATALYSIS, 1996, 162 (02) :339-348
[27]   Higher olefin hydroformylation in organic/aqueous biphasic system accelerated by double long-chain cationic surfactants [J].
Fu, Haiyan ;
Li, Min ;
Chen, Hua ;
Li, Xianjun .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2006, 259 (1-2) :156-160
[28]  
Gartner R., 1982, [No title captured], Patent No. [DE 32 35 030 Al, 3235030]
[29]   Accelerated biphasic hydroformylation by vesicle formation of amphiphilic diphosphines [J].
Goedheijt, MS ;
Hanson, BE ;
Reek, JNH ;
Kamer, PCJ ;
van Leeuwen, PWNM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (08) :1650-1657
[30]   A carbon-carbon coupling reaction catalyzed by a water soluble rhodium catalyst entrapped in mesoporous silica [J].
Handa, P. ;
Stjerndahl, M. ;
Holmberg, K. .
MICROPOROUS AND MESOPOROUS MATERIALS, 2007, 100 (1-3) :146-153