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


ABSTRACT: The cationic N3-species [(p-HC6F4)3PN3]+ (1) featuring a perfluoro-arene phosphonium group serves as a N3+-source in stoichiometric reactions with several Lewis bases (L) allowing for the stepwise formation of [(L)N3]+ and [(L)2N3]+ cations (L = phosphine, carbene) with liberation of (p-HC6F4)3P. X-Ray diffraction analysis and computational studies provide insight into the bonding in these remarkably stable azido-cations.

SUBMITTER: Winkelhaus D 

PROVIDER: S-EPMC6054069 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

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Phosphine and carbene azido-cations: [(L)N<sub>3</sub>]<sup>+</sup> and [(L)<sub>2</sub>N<sub>3</sub>].

Winkelhaus Daniel D   Holthausen Michael H MH   Dobrovetsky Roman R   Stephan Douglas W DW  

Chemical science 20150721 11


The cationic N<sub>3</sub>-species [(<i>p</i>-HC<sub>6</sub>F<sub>4</sub>)<sub>3</sub>PN<sub>3</sub>]<sup>+</sup> (<b>1</b>) featuring a perfluoro-arene phosphonium group serves as a N<sub>3</sub><sup>+</sup>-source in stoichiometric reactions with several Lewis bases (L) allowing for the stepwise formation of [(L)N<sub>3</sub>]<sup>+</sup> and [(L)<sub>2</sub>N<sub>3</sub>]<sup>+</sup> cations (L = phosphine, carbene) with liberation of (<i>p</i>-HC<sub>6</sub>F<sub>4</sub>)<sub>3</sub>P. X-Ray  ...[more]

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