The direct electrochemical synthesis of triphenylphosphine adducts of Group IB monohalides

  • Khan M
  • Oldham C
  • Tuck D
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Abstract

The electrochemical oxidation of copper, silver, or gold into acetonitrile solutions of benzyl chloride or hydrogen halide plus triphenylphosphine leads to the formation of the adducts MXL n (M = Cu, Ag, Au; X = Cl, Br, I; L = Ph 3 P; n = 1, 1.5, 2; not all combinations). The value of n depends markedly on the mole ratio Ph 3 P:dissolved metal. The reaction pathway is discussed in the light of measurements of current efficiency. The results of X-ray structural studies of AuCl•L and AuClL 2 are briefly reported.

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Khan, M., Oldham, C., & Tuck, D. G. (1981). The direct electrochemical synthesis of triphenylphosphine adducts of Group IB monohalides. Canadian Journal of Chemistry, 59(18), 2714–2718. https://doi.org/10.1139/v81-391

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