Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases p. 2583 - 2592 (1982)
Update date:2022-08-11
Topics:
Kapteijn, F.
Mol, J.C.
The selective formation of geometrical product isomers in the methathesis if both propene and pent-2-ene (cis and trans) was studied over several solid catalysts. trans- And cis-but-2-ene were formed in nearly equal amounts from propene, although there were some differences between Re2O7/γ-Al2O3, WO3/SiO2 and MoO3/SiO2 catalysts.The initial trans/cis ratio, (t/c)0, for but-2-ene appeared to be independent of the reaction temperature and the propene pressure.Over Re2O7/γ-Al2O3 cis-pent-2-ene gave (t/c)0 values for but-2-ene (B) and hex-3-ene (H) of 0.35-0.40 and 0.95-1.1, respectively.Starting with trans-pent-2-ene a preference was observed for the formation of trans-products: (c/t)0B = 0.30 and (c/t)0H = 0.12.The weight content of the active phase in the catalyst had no influence on the stereoselectivity, indicating that the active centres have a very distinct character.These results are explained using a stereochemical model based on metallacyclobutane intermediate.The governing factors in the selectivity of product formation are the repulsive interactions between the alkyl substituents of the intermediate structure and the interactions of the substituents with the catalyst surface.
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