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Facile Hydrolysis and Alcoholysis of Palladium Acetate
Authors:Prof. Dr. Robin B. Bedford  John G. Bowen  Russell B. Davidson  Dr. Mairi F. Haddow  Annabelle E. Seymour‐Julen  Dr. Hazel A. Sparkes  Dr. Ruth L. Webster
Affiliation:1. School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS (UK);2. Present address: Department of Chemistry, University of Bath, Bath BA2 7AY (UK)
Abstract:Palladium(II) acetate is readily converted into [Pd32‐OH)(OAc)5] ( 1 ) in the presence of water in a range of organic solvents and is also slowly converted in the solid state. Complex 1 can also be formed in nominally anhydrous solvents. Similarly, the analogous alkoxide complexes [Pd32‐OR)(OAc)5] ( 3 ) are easily formed in solutions of palladium(II) acetate containing a range of alcohols. An examination of a representative Wacker‐type oxidation shows that the Pd‐OH complex 1 and a related Pd‐oxo complex 4 can be excluded as potential catalytic intermediates in the absence of exogenous water.
Keywords:acetate ligands  homogeneous catalysis  hydrolysis  oxidation  palladium
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