New insights into the mechanism of methane formation in the protonation of methyl complexes†

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Richard A. Henderson and Kay E. Oglieve


Abstract

The reaction between [NiMe{(Ph2PCH2CH2)2PPh}]+ and anhydrous HCl (in MeCN) involves initial protonation of nickel to form [Ni(H)Me{(Ph2PCH2CH2)2PPh}]2+, but methane is not produced until after additional, direct protonation of the methyl group.


References

  1. J. K. Kochi, Organometallic Mechanisms and Catalysis, Academic Press, New York, 1978, p. 293 and references therein Search PubMed.
  2. G. S. Hill, L. M. Rendina and R. J. Puddephatt, Organometallics, 1995, 14, 4966 CrossRef CAS and references therein.
  3. M. W. Holtcamp, J. A. Labinger and J. E. Bercaw, Inorg. Chim. Acta, 1997, 265, 117 CrossRef CAS and references therein.
  4. K. W. Kramarz and J. R. Norton, Prog. Inorg. Chem., 1994, 42, 1 CAS and references therein.
  5. R. A. Henderson, Angew. Chem., Int. Ed. Engl., 1996, 35, 946 CrossRef CAS and references therein.
  6. X.-Z. Sun, D. C. Grills, S. M. Nikiforov, M. Poliakoff and M. W. George, J. Am. Chem. Soc., 1997, 119, 7521 CrossRef CAS and references therein.
  7. S. Geftakis and G. E. Ball, J. Am. Chem. Soc., 1998, 120, 9953 CrossRef CAS and references therein.
  8. K. Izutsu, Acid–Base Dissociation Constants in Dipolar Aprotic Solvents, 1990, Blackwell Scientific, Oxford, 1990 Search PubMed.
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