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Bi−P Bond Homolysis as a Route to Reduced Bismuth Compounds and Reversible Activation of P4
Authors:Ryan J. Schwamm  Dr. Matthias Lein  Dr. Martyn P. Coles  Dr. Christopher M. Fitchett
Affiliation:1. School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, New Zealand;2. Department of Chemistry, University of Canterbury, Christchurch, New Zealand
Abstract:Bismuth diphenylphosphanides Bi(NONR)(PPh2) (NONR=[O(SiMe2NR)2], R=tBu, 2,6‐iPr2C6H3, Aryl) undergo facile decomposition via single‐electron processes to form reduced Bi and P species. The corresponding derivatives Bi(NONR)(PCy2) are stable. Reaction of the isolated BiII radical .Bi(NONAr) with white phosphorus (P4) proceeds with the reversible and selective activation of a single P?P bond to afford the bimetallic μ,η1:1‐bicyclo[1.1.0]tetraphosphabutane compound.
Keywords:bismuth  bond homolysis  main-group radicals  P4 activation  phosphanides
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