Pd(II) and Rh(I) chelate complexes of the bidentate phosphino-thiourea ligand PhNHC(S)NHCH2CH2PPh2:: structural properties and activity in homogeneous and hybrid catalysis

被引:19
作者
Cauzzi, D
Costa, M
Cucci, N
Graiff, C
Grandi, F
Predieri, G
Tiripicchio, A
Zanoni, R
机构
[1] Univ Parma, CNR, Ctr Studio Strutturist Diffrattometr, Dipartimento Chim Gen & Inorgan Chim Analit Chim, I-43100 Parma, Italy
[2] Univ Parma, Dipartimento Chim Organ & Ind, I-43100 Parma, Italy
[3] Univ Rome La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
关键词
thiourea functions; bidentate ligand; umbrella arrangement; sol-gel materials;
D O I
10.1016/S0022-328X(99)00615-4
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The new bifunctional ligand PhNHC(S)NHCH2CH2PPh2 (Ptu), containing the thiourea and the phosphine functions, and its Pd(II) and Rh(I) complexes were prepared. Ptu behaves as a bidentate ligand forming seven-membered chelation rings in a boat-like conformation. In the case of palladium, this was ascertained by the X-ray determination of the structure of the complexes [Pd(Ptu)(2)]Cl-2. 6CHCl(3) (1), [Pd(Ptu)(2)Cl]Cl . EtOH (2) and [Pd(Ptu)(2)][CoCl4]. CHCl3. 2EtOH (3). In complexes 1 and 3, the two ligands are related centrosymmetrically, whereas in 2 they are folded by the same side in an umbrella arrangement. The Rh(I) complexes [Rh(cod)(Ptu)]X (X = Cl or PF6; cod = 1,5-ciclooctadiene) and [Rh(cod)(Ptu)](2)[CoCl4] were characterized by P-31-NMR and FT-IR spectroscopy. The catalytic activity in homogeneous hydrogenation and hydroformylation reactions of the Pd(II) and Rh(I) complexes was dependent on the counter-anion, being very low in the case of Cl- and high in the case of non-coordinating anionic groups such as CoCl4- and PF6-. The related ligand (EtO)(3)Si(CH2)(3)NHC(S)NHCH2CH2PPh2 (SiPtu) was sol-gel processed giving hybrid inorganic-organic xerogels (XGPtu). Anchored Pd(II) and Rh(I) complexes were obtained by two procedures: by treating XGPtu with solution of precursor complexes or by sol-gel processing previously prepared SiPtu complexes. Palladium complexes of the thiourea ligand (EtO)(3)Si(CH2)(3)NHC(S)NHPh (Siphtu), with different S-Pd ratios, were also sol-gel processed. The rhodium containing xerogel was found to be an active catalyst for the hydroformylation of styrene, but metal leaching occurred, even if to a limited extent. In the case of Pd-containing materials, it was ascertained that the heterogeneous hydrogenating activity depends on the presence of colloidal metal particles, which form when the metal species are not adequately surrounded by the P,S- or S-ligands. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:431 / 444
页数:14
相关论文
共 31 条
[1]   CIS-[RHI(CO)(PH(2)PCH(2)P(S)PH(2))] - A NEW CATALYST FOR METHANOL CARBONYLATION [J].
BAKER, MJ ;
GILES, MF ;
ORPEN, AG ;
TAYLOR, MJ ;
WATT, RJ .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (02) :197-198
[2]   Diphosphine derivatives of urea and thiourea [J].
Bhattacharyya, P ;
Slawin, AMZ ;
Smith, MB ;
Williams, DJ ;
Woollins, JD .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1996, (18) :3647-3651
[3]   REACTIVITY OF DOUBLE THIOUREAS TOWARDS METAL-COMPLEXES - SYNTHESIS AND CRYSTAL-STRUCTURE OF [((MU-H)RU3(CO)9)2(SC(NPH)N(ET)(CH2)2NH(PHN)CS)] [J].
BORONI, E ;
PREDIERI, G ;
TIRIPICCHIO, A ;
CAMELLINI, MT .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1993, 451 (1-2) :163-168
[4]   IDENTIFICATION OF A SURFACE ORGANOMETALLIC SPECIES ANCHORED ON A THIOUREA-FUNCTIONALIZED SILICA XEROGEL - CRYSTAL-STRUCTURE OF THE MODEL-COMPOUND [(MU-H)RU3(MU-3-SC(NHPR)NPH)(CO)9] [J].
BORONI, E ;
PREDIERI, G ;
TRIPICCHIO, A ;
CAMELLINI, MT .
ORGANOMETALLICS, 1992, 11 (10) :3456-3458
[5]  
CAUQUI MA, 1992, J NONCRYST SOLIDS, V147, P148
[6]   FORMATION OF AN ANCHORED COPPER(II) COMPLEX ON A THIOUREA-FUNCTIONALIZED SILICA-GEL BY IN-SITU MODIFICATION OF THE TETHERED LIGATING FUNCTION [J].
CAUZZI, D ;
PREDIERI, G ;
TIRIPICCHIO, A ;
ZANONI, R ;
GIORI, C .
INORGANICA CHIMICA ACTA, 1994, 221 (1-2) :183-186
[7]   SULFUR LIGAND-STABILIZED PALLADIUM AGGREGATES PRODUCED ON THE SURFACE OF BENZOYLTHIOUREA-FUNCTIONALIZED SILICA XEROGELS [J].
CAUZZI, D ;
MARZOLINI, G ;
PREDIERI, G ;
TIRIPICCHIO, A ;
COSTA, M ;
SALVIATI, G ;
ARMIGLIATO, A ;
BASINI, L ;
ZANONI, R .
JOURNAL OF MATERIALS CHEMISTRY, 1995, 5 (09) :1375-1381
[8]   Anchoring rhodium(I) on thiourea-functionalized silica xerogels and silsesquioxanes .2. Matrix effects on the selectivity in the hydroformylation of styrene [J].
Cauzzi, D ;
Costa, M ;
Gonsalvi, L ;
Pellinghelli, MA ;
Predieri, G ;
Tiripicchio, A ;
Zanoni, R .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1997, 541 (1-2) :377-389
[9]  
CAUZZI D, 1993, GAZZ CHIM ITAL, V123, P713
[10]   ANCHORING RHODIUM(I) ON BENZOYLTHIOUREA-FUNCTIONALIZED SILICA XEROGELS - PRODUCTION OF RECYCLABLE HYDROFORMYLATION CATALYSTS AND THE CRYSTAL-STRUCTURE OF THE MODEL-COMPOUND [RH(COD)(HBZTU)CL] [J].
CAUZZI, D ;
LANFRANCHI, M ;
MARZOLINI, G ;
PREDIERI, G ;
TIRIPICCHIO, A ;
COSTA, M ;
ZANONI, R .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1995, 488 (1-2) :115-125