Abstract

This study discusses the hydroformylation of styrene using rhodium systems containing four structurally related diphosphines: 1,2-bis(diphenylphosphine)ethane 1 (dppe), 1,3-bis(diphenylphosphine)propane 2 (dppp), ( R, R)-2,3-bis(diphenylphosphine)butane 3 (chiraphos) and ( S, S)-2,4-bis(diphenylphosphine)pentane 4 (bdpp). A systematic analysis of the effect of the pressure, temperature and the ligand to metal molar ratio for these catalytic systems shows that the five- and six-membered ring chelating diphosphines behave different. The regio- and enantioselectivity observed provide evidence of the catalytic species involved in the process. By analyzing the selectivity of the catalytic systems formed by mixing PEtPh 2 and the chiral diphosphine ligands, we propose a model describing the equilibria among the catalytic species.

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