SYNTHESIS OF RHODIUM(I) COMPLEXES WITH THE NEW DITHIOL CHIRAL LIGAND TRANS-2,3-BIS(MERCAPTOMETHYL)-BICYCLO[2.2.2]OCTANE (H2BCOS) - THEIR APPLICATION AS CATALYSTS PRECURSORS IN THE STYRENE HYDROFORMYLATION())

Citation
A. Castellanospaez et al., SYNTHESIS OF RHODIUM(I) COMPLEXES WITH THE NEW DITHIOL CHIRAL LIGAND TRANS-2,3-BIS(MERCAPTOMETHYL)-BICYCLO[2.2.2]OCTANE (H2BCOS) - THEIR APPLICATION AS CATALYSTS PRECURSORS IN THE STYRENE HYDROFORMYLATION()), Journal of organometallic chemistry, 539(1-2), 1997, pp. 1-7
Citations number
38
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
ISSN journal
0022328X
Volume
539
Issue
1-2
Year of publication
1997
Pages
1 - 7
Database
ISI
SICI code
0022-328X(1997)539:1-2<1:SORCWT>2.0.ZU;2-Z
Abstract
The new dithiol ligand (+)-H2BCOS ((+)-1) has been synthesized. The te tranuclear rhodium complex [Rh-2(mu-BCOS)(cod)(2)](2) (8) (cod = cyclo octa-1,5-diene) was prepared by starting with the dinuclear complex [R h(mu-OMe)(cod)](2) (7) through an exchange reaction with the dithiol l igand, The reactivity of 8 towards CO and phosphorus-donor ligands was studied; the mixed CO/P complex [Rh-2(mu-BCOS)(CO)(2)(PPh3)(2)] (10) was prepared and studied by IR and P-31 NMR. The [Rh-2(mu-(+)-BCOS)(co d)(2)](2) complex was tested as a catalyst precursor in the enantiosel ective hydroformylation of styrene, The influence of P-donor as modify ing ligand, temperature and pressure on the catalytic activity and sel ectivity was explored, achieving ee up to 55% with total conversion in to aldehydes in the presence of BDPP. These results revealed a slight cooperative effect between the dithiolate and the diphosphine ligands. (C) 1997 Elsevier Science S.A.