Heterobimetallic intermediates in alkene insertion reactions into a Pd–acetyl bond

Abstract
The reactivity of diphosphine-bridged heterobimetallic Fe–Pd alkyl complexes was evaluated for the insertion of CO, isonitriles, ethylene, methyl acrylate and norbornadienes and the crystal structures of the precursor alkyl complex, the iminoacyl derivative and the five-membered ring complex resulting from ethylene insertion into the palladium–acyl bond are reported.

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