New rhodium complexes with P,N-ligands possessing a hydroxy or methoxy group.: Synthesis, characterization and application to hydroformylation of styrene

被引:46
作者
Kostas, ID [1 ]
Screttas, CG [1 ]
机构
[1] Natl Hellen Res Fdn, Inst Organ & Pharmaceut Chem, GR-11635 Athens, Greece
关键词
phosphine; hemilabile ligand; rhodium; catalysis; hydroformylation;
D O I
10.1016/S0022-328X(99)00181-3
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new cationic rhodium(I) complexes containing a phosphino amino alcohol ligand and a methoxy amino phosphine, respectively, have been prepared. According to IR and NMR data the ligands are P,N-bonded and coordination of the hydroxy or the methoxy group to the metal does not take place. The complexes were applied to the hydroformylation of styrene and displayed a quantitative chemoselectivity for aldehydes with a very good branched:linear ratio. The reaction rate is higher using the complex possessing the methoxy group as opposed to the hydroxy group. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 15 条
[1]   Synthesis of new phosphino amino alcohol ligands via ortho-alkyllithiation reactions. Versatile coordination behavior toward copper(I) and palladium(II) [J].
Andrieu, J ;
Steele, BR ;
Screttas, CG ;
Cardin, CJ ;
Fornies, J .
ORGANOMETALLICS, 1998, 17 (05) :839-845
[2]   CYCLOOCTATETRAENE-RHODIUM(I) COMPLEXES [J].
BENNETT, MA ;
SAXBY, JD .
INORGANIC CHEMISTRY, 1968, 7 (02) :321-&
[3]   COMPLEXATION OF ENANTIOMER-FREE CIS-3-DIPHENYLPHOSPHINO-4-HYDROXYTETRAHYDROFURANS AND TRANS-3-DIPHENYLPHOSPHINO-4-HYDROXYTETRAHYDROFURANS WITH [RH(COD)(2)]BF4 [J].
BORNER, A ;
KLESS, A ;
HOLZ, J ;
BAUMANN, W ;
TILLACK, A ;
KADYROV, R .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 490 (1-2) :213-219
[4]  
Borns S, 1998, EUR J INORG CHEM, P1291
[5]  
FROHNING CD, 1996, HYDROFORMYLATION APP, V1, P88
[6]   DI-MU-CHLORO-BIS(ETA-4-1,5-CYCLOOCTADIENE)DIRHODIUM(I) [J].
GIORDANO, G ;
CRABTREE, RH .
INORGANIC SYNTHESES, 1990, 28 :88-90
[7]   CATIONIC TRANSITION-METAL COMPLEXES .1. SYNTHESIS AND REACTIONS OF BIS(DIENE)-RHODIUM AND BIS(DIENE)-IRIDIUM TETRAFLUOROBORATES [J].
GREEN, M ;
KUC, TA ;
TAYLOR, SH .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1971, (14) :2334-&
[8]   Influence of a remote hydroxy group in the ligand on the reactivity of a chiral hydrogenation catalyst [J].
Heller, D ;
Holz, J ;
Borns, S ;
Spannenberg, A ;
Kempe, R ;
Schmidt, U ;
Borner, A .
TETRAHEDRON-ASYMMETRY, 1997, 8 (02) :213-222
[9]   HYDROXYALKYLPHOSPHINES IN ASYMMETRIC HYDROGENATIONS [J].
HOLZ, J ;
BORNER, A ;
KLESS, A ;
BORNS, S ;
TRINKHAUS, S ;
SELKE, R ;
HELLER, D .
TETRAHEDRON-ASYMMETRY, 1995, 6 (08) :1973-1988
[10]   Rhodium COD complexes of mixed donor set tripod ligands: coordination chemistry and catalysis [J].
Jacobi, A ;
Huttner, G ;
Winterhalter, U .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1998, 571 (02) :231-241