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Publication - Dr Chris Russell

    A Transient Vinylphosphinidene via a Phosphirene-Phosphinidene Rearrangement

    Citation

    Liu, LL, Zhou, J, Cao, LL, Andrews, R, Falconer, RL, Russell, CA & Stephan, DW, 2018, ‘A Transient Vinylphosphinidene via a Phosphirene-Phosphinidene Rearrangement’. Journal of the American Chemical Society, vol 140., pp. 147-150

    Abstract

    A room-temperature-stable crystalline 2H-phosphirene (1) was prepared by treatment of an electrophilic diamidocarbene with tert-butylphosphaalkyne. Compound 1 is shown to react as a vinylphosphinidene generated via phosphirene-phosphinidene rearrangement. Thermolysis is shown to affect C-N bond scission while reactions with C6Cl4O2 or (tht)AuCl afford formal oxidation of the phosphindene center and the phosphinidene-insertion into an aromatic C-C bond of a mesityl group, respectively. The latter reaction is the first example of a phosphorus analog of the Büchner ring expansion reaction.

    Full details in the University publications repository