Cooperativity in Rh2 Complexes: High Catalytic Activity and High Regioselectivity in the Hydroformylation of Olefins
✍ Scribed by Prof. Dr. Georg Süss-Fink
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 252 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
✦ Synopsis
An important step forward in the search for catalytically active polynuclear metal complexes has been made by George G. Stanley's group: The bimetallic complex cations r~c-[Rh,(nbd),L]~+ l r and rne~o-[Rh,(nbd),L]~+ l m (nbd = norbornadiene) which were isolated as tetrafluoroborates (Scheme l),[l1 were obtained by reacting bis(norbornadiene)rhodium tetrafluoroborate with a new tetraphosphane ligand L which exists in R,R, S,S and R,S forms and can be separated into racemic (R,R/S,S) and meso structures (R,S).['] r a c -( R . R / Et , P -Rh Rh -PEt, Et\ /pEt2 <jWP, 'J /pvp\ph Ph Ph Ph r a c -l r meso-(R,S)-L Scheme 1. The tetrdphosphdne ligand L and the hydroformylation-active dirhodium complex I r .
📜 SIMILAR VOLUMES
Cationic rhodium(i) complexes cis-[Rh(acetone) 2 (L)(L')] (2: L L' C 8 H 14 ; 3: L C 8 H 14 ; L' PiPr 3 ; 4: L L' PiPr 3 ), prepared from [{RhCl-(C 8 H 14 ) 2 } 2 ] and isolated as PF 6 salts, catalyze the CÀC coupling reaction of diphenyldiazomethane with ethene, propene, and styrene. In most cases
The preparation and catalytic evaluation of the three group 9 (cyclopentadienyl)metal(trimethylvinylsilane) complexes of the type C 5 H 5 M(H 2 C= CHSiMe 3 ) 2 (M = cobalt, rhodium and iridium) are reported. The complexes were investigated in [2 + 2 + 2] cycloaddition as well as in hydrogenation, hy