Hydroformylation of functional alkenes with heterodonor phosphine rhodium catalysts: substrate or ligand directed regioselectivity?

• Published in: Catalysis letters Vol. 70; no. 3-4; pp. 149 - 154
• Main Authors: Reinius, H K, Krause, AOI
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Nature B.V 01.01.2000
• Subjects: Alkenes; Anhydrides; Catalysis; Catalysts; Catalytic activity; Chemical industry; Cyclohexene; Esters; Ligands; Polymethyl methacrylate; Regioselectivity; Rhodium; Selectivity; Styrenes; Substrates
• ISSN: 1011-372X; 1572-879X
• DOI: 10.1023/A:1018841418819

The catalytic activity and selectivity of heterodonor phosphine rhodium catalysts prepared in situ were tested in the hydroformylation of functional alkenes (ethyl acrylate, methyl methacrylate, styrene, 4-vinyl-1-cyclohexene, dicyclopentadiene and cis-1,2,3,6-tetrahydrophthalic anhydride). Systematic variation of the heterodonor atom in the ortho position of the ligand showed that the heterodonor atom has a significant influence on the activities and selectivities of the reaction. However, the activity seems to depend mainly on the modifying ligand, and the regioselectivity mainly on the substrate (i.e., the structure and functionality of the alkene). Nevertheless, regioselective control is only obtained through synergy between the substrate and the catalyst. Clear regiocontrol was observed in the hydroformylation of α,β-unsaturated esters and styrene with an in situ formed o-(thiomethylphenyl)diphenylphosphine rhodium catalyst.