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Hydroformylation of alkenes by use of rhodium complex catalysts

Evans, D., Osborn, J. A., Wilkinson, G.·1968·Journal of the Chemical Society A: Inorganic, Physical, Theoretical

Abstract

The use of complexes of rhodium of the type trans-RhX(CO)(PR3)2, (X = halogen, R = aryl) as hydroformylation catalysts for alkenes is studied. It is shown that an inhibition period is removed by addition of hydrogen halide acceptors and that the halide complex undergoes hydrogenolysis to form a hydrido-species. The hydrido-species is only one of several complexes in equilibrium but it appears that the principal active catalytic species is RhH(CO)2(PPh3)2. This species is formed by addition of carbon monoxide to the monocarbonyl complex RhH(CO)(PPh3)2. The latter is also formed by dissociation when the stable crystalline complex RhH(CO)(PPh3)3 is dissolved in benzene or other solvents. With RhH(CO)(PPh3)3 as catalyst, alkenes undergo rapid hydroformylation even at 25°/1 atm.; with alk-1-enes the ratio of straight- to branched-chain aldehyde formed is considerably higher than the ratios normally found in hydroformylation reactions, being ca. 20 at 25°. Hydrogen atom exchange and isomerisation reactions of alkenes with RhH(CO)(PPh3)3 are described.

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Metadata

Authors
Evans, D., Osborn, J. A., & Wilkinson, G.
Venue
Journal of the Chemical Society A: Inorganic, Physical, Theoretical
Published
1968
Pages
3133
ISSN
0022-4944 (ISSN-L)
OpenAlex
W2005753110
Cited by
683
References
0
FWCI
5.16
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Hydroformylation of alkenes by use of rhodium complex catalysts. https://app.cochat.ai/papers/10.1039/j19680003133
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Evans, D., Osborn, J. A., & Wilkinson, G. (1968). Hydroformylation of alkenes by use of rhodium complex catalysts. Journal of the Chemical Society A: Inorganic, Physical, Theoretical. https://doi.org/10.1039/j19680003133

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