Fragmentation of an N-Substituted One-Coordinate Phosphorus (Phosphaalkyne): Plausible Generation of Monovalent Phosphorus Species
datasetposted on 27.09.2010, 00:00 by Alex S. Ionkin, William J. Marshall, Brian M. Fish, Laurie A. Howe
A new one-step synthesis of a stable nitrogen-substituted phosphaalkyne (5) was developed, by the condensation of CsF (2), tris(trimethylsilyl)phosphine (3), and supermesityl isocyanate (4). Compound 5 has the longest terminal CP bond (1.617 Å) of any phosphaalkyne. Due to electron delocalization on the terminal phosphorus atom in 5, fragmentation to a monovalent phosphorus species (CsP (9)) and supermesityl isonitrile (8) is plausible. Isonitrile (8) was isolated in pure form. CsP (9) was trapped as a tricesium pentaphosphorus compound (10) and also as cesium [1,2,4]triphospholide (13).
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isonitrilecompoundtriselectron delocalizationCsFphosphaalkyneIsonitrileCsPsynthesismonovalent phosphorus speciesFragmentationtricesiumisocyanatetriphospholideCPpentaphosphoruterminal phosphorus atomfragmentationcondensationGenerationMonovalent Phosphorus SpeciesAPlausiblesupermesitylDuecesiumPhosphaalkynebond