Selective Functionalization of P4 by Metal‐Mediated CP Bond Formation |
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Authors: | Sebastian Heinl Sabine Reisinger Dr. Christoph Schwarzmaier Dr. Michael Bodensteiner Prof. Dr. Manfred Scheer |
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Affiliation: | Institute of Inorganic Chemistry, University of Regensburg, 93040 Regensburg (Germany) |
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Abstract: | A new and selective one‐step synthesis was developed for the first activation stage of white phosphorus by organic radicals. The reactions of NaCpR with P4 in the presence of CuX or FeBr3 leads to the clean formation of organic substituted P4 butterfly compounds CpR2P4 (CpR: CpBIG=C5(4‐nBuC6H4)5 ( 1 a ), Cp′′′=C5H2tBu3 ( 1 b ), Cp*=C5Me5 ( 1 c ) und Cp4iPr=C5HiPr4 ( 1 d )). The reaction proceeds via the activation of P4 by CpR radicals mediated by transition metals. The newly formed organic derivatives of P4 have been comprehensively characterized by NMR spectroscopy and X‐ray crystallography. |
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Keywords: | organophosphorus compounds P4 activation phosphorus radicals |
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