Journal article

Decarboxylative-coupling of allyl acetate catalyzed by group 10 organometallics, [(phen)M(CH3)]

M Woolley, A Ariafard, GN Khairallah, KH Kwan, PS Donnelly, JM White, AJ Canty, BF Yates, RAJ O'Hair

Journal of Organic Chemistry | Published : 2014

Abstract

Gas-phase carbon-carbon bond forming reactions, catalyzed by group 10 metal acetate cations [(phen)M(O2CCH3)]+ (where M = Ni, Pd or Pt) formed via electrospray ionization of metal acetate complexes [(phen)M(O2CCH3)2], were examined using an ion trap mass spectrometer and density functional theory (DFT) calculations. In step 1 of the catalytic cycle, collision induced dissociation (CID) of [(phen)M(O2CCH3)]+ yields the organometallic complex, [(phen)M(CH3)]+, via decarboxylation. [(phen)M(CH3)]+ reacts with allyl acetate via three competing reactions, with reactivity orders (% reaction efficiencies) established via kinetic modeling. In step 2a, allylic alkylation occurs to give 1-butene and r..

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Grants

Awarded by Australian Respiratory Council


Funding Acknowledgements

We thank Dr. Gabriel da Silva for discussions on the kinetic modelling and the ARC for financial support via Grants DP110103844 (to R.A.J.O. and G.N.K.) and DP1096134 (to G.N.K) and through the ARC CoE program and Grant DP120101540 (A.J.C. and B.F.Y.). M.W. thanks the Faculty of Science for a Melbourne Research Scholarship. The authors gratefully acknowledge the generous allocation of computing time from the Victorian Partnership for Advanced Computing (VPAC) Facility, the University of Tasmania, and the National Computing Infrastructure.