Pd(II)-Schiff base complexes heterogenised on MCM-41 and delaminated zeolites as efficient and recyclable catalysts for the Heck reaction

被引:100
作者
González-Arellano, C
Corma, A
Iglesias, M
Sánchez, F
机构
[1] CSIC, Inst Quim Organ Gen, E-28006 Madrid, Spain
[2] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
[3] CSIC, Inst Ciencia Mat, E-28049 Madrid, Spain
关键词
Heck reaction; heterogenisation; immobilised; palladium; Schiff bases; Suzuki coupling;
D O I
10.1002/adsc.200404119
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We present a widely applicable approach for the preparation of Pd-complexes supported on silica-based mesoporous and laminar inorganic solids (silica gel, purely siliceous and acidic MCM-41, and delaminated zeolites ITQ-2 and ITQ-6) which involves the use of the Schiff bases 2-tert-butyl-4-methyl-6{(E)-[(2S)-1-(1-arylmethyl)pyrrolidinyl]imino}methylphenol (aryl=phenyl, 1-naphthyl, 2-naphthyl) as anchored ligands. As an extension of our research in "recyclable catalytic systems" we report results demonstrating the reactivity and recyclability of these systems for the Heck reaction (in a biphasic mode using ethylene glycol and toluene) and Suzuki coupling under phosphine-free conditions. The complexes are insensitive to oxygen or moisture, and no change of their activity was observed when exposed to an open system during the usual operation. No palladium black was observed after an extended reaction time and no residual palladium was detected from the filtrate at the end of the reaction.
引用
收藏
页码:1758 / 1764
页数:7
相关论文
共 63 条
[1]   New Mn(II) and Cu(II) chiral C2-multidentate complexes immobilised in zeolites (USY, MCM41) -: Reusable catalysts for selective oxidation reactions [J].
Alcón, MJ ;
Corma, A ;
Iglesias, M ;
Sánchez, F .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2003, 194 (1-2) :137-152
[2]   Anionic Pd(0) and Pd(II) intermediates in palladium-catalyzed Heck and cross-coupling reactions [J].
Amatore, C ;
Jutand, A .
ACCOUNTS OF CHEMICAL RESEARCH, 2000, 33 (05) :314-321
[3]   Catalysis as a foundational pillar of green chemistry [J].
Anastas, PT ;
Kirchhoff, MM ;
Williamson, TC .
APPLIED CATALYSIS A-GENERAL, 2001, 221 (1-2) :3-13
[4]   Hybrid organic -: inorganic catalysts:: a cooperative effect between support, and palladium and nickel salen complexes on catalytic hydrogenation of imines [J].
Ayala, V ;
Corma, A ;
Iglesias, M ;
Rincón, JA ;
Sánchez, F .
JOURNAL OF CATALYSIS, 2004, 224 (01) :170-177
[5]   A NEW FAMILY OF MESOPOROUS MOLECULAR-SIEVES PREPARED WITH LIQUID-CRYSTAL TEMPLATES [J].
BECK, JS ;
VARTULI, JC ;
ROTH, WJ ;
LEONOWICZ, ME ;
KRESGE, CT ;
SCHMITT, KD ;
CHU, CTW ;
OLSON, DH ;
SHEPPARD, EW ;
MCCULLEN, SB ;
HIGGINS, JB ;
SCHLENKER, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10834-10843
[6]   The heck reaction as a sharpening stone of palladium catalysis [J].
Beletskaya, IP ;
Cheprakov, AV .
CHEMICAL REVIEWS, 2000, 100 (08) :3009-3066
[7]   Catalyst product separation techniques in Heck reaction [J].
Bhanage, BM ;
Arai, M .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 2001, 43 (03) :315-344
[8]   Heck reactions with various types of palladium complex catalysts: application of multiphase catalysis and supercritical carbon dioxide [J].
Bhanage, BM ;
Fujita, S ;
Arai, M .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2003, 687 (02) :211-218
[9]   Comparison of activity and selectivity of various metal-TPPTS complex catalysts in ethylene glycol - Toluene biphasic Heck vinylation reactions of iodobenzene [J].
Bhanage, BM ;
Zhao, FG ;
Shirai, M ;
Arai, M .
TETRAHEDRON LETTERS, 1998, 39 (51) :9509-9512
[10]  
Brase S, 1998, METAL-CATALYZED CROSS-COUPLING REACTIONS, P99