Synthesis, structure and catalytic application of palladium(II) complexes bearing N-heterocyclic carbenes and phosphines

被引:309
作者
Herrmann, WA
Böhm, VPW
Gstöttmayr, CWK
Grosche, M
Reisinger, CP
Weskamp, T
机构
[1] Tech Univ Munich, Inst Anorgan Chem, D-85747 Garching, Germany
[2] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[3] Bayer AG, Cent Res, D-47812 Krefeld, Germany
[4] Symyx Technol, Santa Clara, CA 95051 USA
关键词
CC-coupling; Heck reactions; N-heterocyclic carbenes; phosphines; palladium;
D O I
10.1016/S0022-328X(00)00722-1
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A variety of mixed palladium(II) complexes bearing N-heterocyclic carbenes (NHCs) and triaryl- and trialkylphosphines [NHC(R-2)]Pd(PR'(3))I-2 (R = Me, t-Bu, (R)-1-phenylethyl; R' = Ph, o-tolyl, cyclohexyl, t-Bu) have been prepared. Crystal structure details of trans-diiodo(1,3-di-tert-butylimidazolin-2-ylidene)(triphenylphosphino)palladium(II) are presented. The complexes were tested as catalysts in the Mizoroki-Heck, Suzuki-Miyaura and Stille reactions as well as in the dimerization of phenylacetylene. In catalytic studies of the Suzuki-Miyaura cross-coupling reaction, the performance of these novel complexes was compared to the results obtained by the corresponding bis(NHC) and bis(phosphine) complexes. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:616 / 628
页数:13
相关论文
共 136 条
  • [1] Ruthenium carbene complexes with imidazolin-2-ylidene ligands allow the formation of tetrasubstituted cycloalkenes by RCM
    Ackermann, L
    Fürstner, A
    Weskamp, T
    Kohl, FJ
    Herrmann, WA
    [J]. TETRAHEDRON LETTERS, 1999, 40 (26) : 4787 - 4790
  • [2] On C-C coupling by carbene-stabilized palladium catalysts: A density functional study of the Heck reaction
    Albert, K
    Gisdakis, P
    Rosch, N
    [J]. ORGANOMETALLICS, 1998, 17 (08) : 1608 - 1616
  • [3] [Anonymous], ANGEW CHEM
  • [4] [Anonymous], ANGEW CHEM
  • [5] [Anonymous], 1998, TRANSITION METALS OR
  • [6] [Anonymous], ANGEW CHEM
  • [7] [Anonymous], ANGEW CHEM
  • [8] [Anonymous], ANGEW CHEM
  • [9] [Anonymous], ANGEW CHEM INT ED EN
  • [10] [Anonymous], ANGEW CHEM