Binuclear and polynuclear rhodium complexes containing chiral dithiolate ligands derived from lactic acid
✍ Scribed by Z. Freixa; E. Martin; S. Gladiali; J. C. Bayón
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 127 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0268-2605
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✦ Synopsis
Two precursors of the chiral dithiolato ligands, di-[(2R)-acetylmercaptopropyl] phthalate and isophthalate, 1 and 2 respectively, were synthesized from (S)-lactic acid. Reactions of 1 and 2 with [Rh 2 (m)-OMe) 2 (cod) 2 ] (cod = 1,5-cyclo-octtadiene) yielded rhodium thiolato complexes of different nuclearities. The mixtures of complexes were analyzed by gel-permeation chromatography (GPC). The reaction with ligand 1 produced a mixture of oligomeric complexes, where the binuclear species was the main component. Higher-nuclearity complexes were the main products of the reaction with ligand 2. The rhodium complexes, in the presence of PPh 3 , were tested as catalyst precursors for the asymmetric hydroformylation of styrene. Moderate activity and regioselectivity were achieved in most cases, but no enantioselective discrimination was observed.
📜 SIMILAR VOLUMES
A series of three new quadridentate ligands was synthesized by reaction of the haloacetylated amino acid esters L- BrAc-Phe-OMe (4a), L-BrAc-Lys(Z)-OMe (4b), and ClAc-Gly-OEt (4c), respectively, with bis(picolyl)amine (bpa, 5). The obtained products L-bpaAc-Phe-OMe (3a), L-bpaAc-Lys(Z)-OMe (3b), and