Abstract
Several μ-thiolato-μ-chlorodicarbonylbis(tri-t-butylphosphine)dirhodium complexes were anchored (a) to diphenylphosphinated crosslinked polystyrene by phosphine ligand exchange, (b) to chloromethylated polystyrene resin by substitution of the benzylic halogen via the μ-thiolato group, and (c) to silica and alumina via a sulfur-attached -CH2CH2SiO3bridge. The catalytic activity of the various immobilized dirhodium complexes in allylic isomerization, hydrogenation and hydroformylation processes were investigated. Some mechanistic features of these catalyses are discussed.
Original language | English |
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Pages (from-to) | 199-212 |
Number of pages | 14 |
Journal | Journal of Molecular Catalysis |
Volume | 43 |
Issue number | 2 |
DOIs | |
State | Published - Dec 1987 |
Externally published | Yes |