The mechanism of the reactions between dppf-Ni0 complexes and alkyl halides has been investigated using kinetic and mechanistic experiments and DFT calculations. The active species is [Ni(κ2-dppf)(κ1-dppf)], which undergoes a halide abstraction reaction with alkyl halides and rapidly captures the alkyl radical that is formed. The rates of the reactions of [Ni(COD)(dppf)] with alkyl halides and the yields of prototypical nickel-catalysed Kumada cross-coupling reactions of alkyl halides are shown to be significantly improved by the addition of free dppf ligand.
Greaves, M.; Ronson, T. O.; Lloyd-Jones, G. C.; Maseras, F.; Sproules, S.; Nelson, D. J.
ACS Catal. 2020, 10 (18), 10717–10725
DOI:
10.1021/acscatal.0c02514
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