Abstract
A kinetic study of the reaction between PdCl2−4 and isoprene is described. The results are interpreted in terms of the formation of two π-complexes between palladium(II) and isoprene, one having only one double bond coordinated to the metal, the other being a chelated diene compound. Nucleophilic attack of solvent methanol on these intermediate complexes gives the methoxy π-allyl complex.
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