An anionic phosphenium complex as an ambident nucleophile. Issue 13 (27th February 2015)

• Record Type: Journal Article
• Authors: Stadelmann, B.; Bender, J.; Förster, D.; Frey, W.; Nieger, M.; Gudat, D.
• Is Part Of: Dalton transactions. Volume 44:Issue 13(2015)
• Page Start: 6023
• Page End: 6031
• Publication Date: 2015-02-27
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c5dt00008d
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Treatment of an N-heterocyclic chlorophosphine with Collman's reagent or K[HFe(CO)4 ]/NaH gave a unique anionic phosphenium complex which behaves as an ambident nucleophile. Abstract : A unique anionic phosphenium complex was prepared from reaction of an N-heterocyclic chlorophosphine with Collman's reagent or K[HFe(CO)4 ]/NaH and characterized by spectral and XRD data. The complex behaves as an ambident nucleophile. Reactions with acetic acid, ClSnPh3, and a further equivalent of an N-heterocyclic chlorophosphine proceed via electrophilic functionalization at the metal site to yield appropriate mono- or bis-phosphenium complexes. Reaction with MeI at −70 °C produces a P-alkylation product as the first spectroscopically detectable intermediate, which decays at a higher temperature to give a mixture of free P-methylated N-heterocyclic phosphine and its Fe(CO)4 complex. The different reaction products were characterized by spectral and XRD data. Computational studies indicate that the NHP units in all complexes display π-acceptor behaviour but show no disposition to adopt phosphide-like character or formally oxidize the metal centre.