4.8 Article

Phosphine and carbene azido-cations: [(L)N3]+ and [(L)2N3]+

Journal

CHEMICAL SCIENCE
Volume 6, Issue 11, Pages 6367-6372

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5sc02336j

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Funding

  1. NSERC of Canada
  2. Canada Research Chair
  3. Alexander von Humboldt Foundation

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The cationic N-3-species [(p-HC6F4)(3)PN3](+) (1) featuring a perfluoro-arene phosphonium group serves as a N-3(+)-source in stoichiometric reactions with several Lewis bases (L) allowing for the stepwise formation of [(L)N-3](+) and [(L)(2)N-3](+) cations (L = phosphine, carbene) with liberation of (p-HC6F4)(3)P. X-Ray diffraction analysis and computational studies provide insight into the bonding in these remarkably stable azidocations.

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