Studies on the characterization of several iridium- and rhodium-clay catalysts and their activity in imine hydrogenation

被引:17
作者
Claver, C
Fernández, E
Margalef-Català, R
Medina, F
Salagre, P
Sueiras, JE
机构
[1] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, Tarragona 43005, Spain
[2] Univ Rovira & Virgili, Escola Tecn Super Engn Quim, Tarragona 43005, Spain
关键词
montmorillonite; bentonite; hectorite; clay; hydrogenation of imines; iridium; rhodium; heterogenized; intercalation; adsorption;
D O I
10.1006/jcat.2001.3221
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
Iridium- and rhodium-clay catalysts were prepared by immobilizing the complexes [Ir(mu -Cl)(COD)](2) [1] + 4PPh(3), [Ir(COD)-(PPh3)(2)]BF4 [2], [Ir(COD)(PPh3)(2)]PF6 [3], and [Rh(COD)(PPh3)(2)]BF4 [4] in montmorillonite K-10 (MK-10), sodium bentonite (Naf-MM), and lithium hectorite (Li+-Hect). Other analogous supports were prepared after thermal and acidic modifications to montmorillonite K-10. For example, MK-10 was calcined at 500 degreesC (MK-10-500) and treated with nitric acid (H-HNO3(+)-MK-10). The supports were characterized using XRD, BET surface area, FTIR, and acidity titration to confirm the properties of smectite-clay materials. The characterization of the immobilized iridium- and rhodium-clays was studied using XRD, FTIR,and conductimetric analyses. From these results, We found that the complexes are adsorbed mainly on the external surface of MK-10 and Li+-Hect. However, the immobilization of the organometallic complexes on Na+-MM is intercalated mainly by the ion-exchange process. Hydrogenation of the aldimine N-benzylidene aniline was studied with the iridium- and rhodium-clay catalytic systems. The aim of our study was to determine how the immobilized system influences the catalytic process, taking into account the metal, the counterion, and the acidity and composition of the support. In some catalytic systems the catalyst was reused for a significant number of consecutive runs. The catalyst 2-MK-10, for example, was reused in consecutive hydrogenations and showed high activity (> 97% conversion) for at least 13 runs. The loss of catalytic activity as a consequence of the relative stability of the metallic intermediate species to air is also discussed. (C) 2001 Academic Press.
引用
收藏
页码:70 / 79
页数:10
相关论文
共 47 条
  • [1] Baird T., 1973, CLAY MINER, V10, P17
  • [2] RHODIUM(I) SULFONATED-BDPP CATALYZED ASYMMETRIC HYDROGENATION OF IMINES IN AQUEOUS ORGANIC 2-PHASE SOLVENT SYSTEMS
    BAKOS, J
    OROSZ, A
    HEIL, B
    LAGHMARI, M
    LHOSTE, P
    SINOU, D
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1991, (23) : 1684 - 1685
  • [3] BAKOS J, 1994, NATO ASI SER, V15, P231
  • [4] Bigelow L. A., 1941, ORG SYNTH, V1, P80
  • [5] Blaser H.-U., 1999, COMPREHENSIVE ASYMME, P247
  • [6] Studies on catalytic asymmetric imine hydrogenation in the presence of reverse micelles: Enhanced enantioselectivity due to surfactant head group coordination
    Buriak, JM
    Osborn, JA
    [J]. ORGANOMETALLICS, 1996, 15 (14) : 3161 - 3169
  • [7] The application of Ir-complexes of trans-2,5-dialkylpyrrolidinyl-benzyldiphenylphosphines to the enantioselective reduction of imines
    Cahill, JP
    Lightfoot, AP
    Goddard, R
    Rust, J
    Guiry, PJ
    [J]. TETRAHEDRON-ASYMMETRY, 1998, 9 (24) : 4307 - 4312
  • [8] CASTILLON S, 2000, P200001396 REPSOLYPF
  • [9] STRUCTURE OF AN IRIDIUM BIS(PHOSPHINE)DIENE COMPLEX, A CATALYST FOR HOMOGENEOUS HYDROGENATION
    CHALONER, PA
    HITCHCOCK, PB
    REISINGER, M
    [J]. ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1992, 48 : 735 - 737
  • [10] SYNTHESIS, REACTIONS AND CATALYTIC ACTIVITIES OF IRIDIUM COMPLEXES INTERCALATED INTO MONTMORILLONITE
    CHIN, CS
    LEE, BG
    YOO, IY
    KWON, TH
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1993, (04): : 581 - 585