A Persistent 1,2-Dihydrophosphasilene Adduct

Kerstin Hansen, Tibor Szilvasi, Burgert Blom, Matthias Driess*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The reaction of the arylchlorosilylene-NHC adduct ArSi(NHC)Cl [Ar = 2,6-Trip(2)-C6H3; NHC = (MeC)(2-)(NMe)(2)C] 1 with one molar equiv of LiPH2. dme (dme = 1,2dimethoxyethane) affords the first 1,2-dihydrophosphasilene adduct 2 (ArSi(NHC)(H)=PH). The latter is labile in solution and can undergo head-to-tail dimerization to give [ ArSi( H)PH](2) 3 and "free" NHC. Further stabilization of 2 by complexation with {W(CO)(5)} affords the isolable 1,2-dihydrophosphasilene- tungsten complex 4 [ArSi(NHC)(H)=P(H) W( CO) 5]. Additionally, the new 1-silyl-2-hydrophosphasilene ArSi(NHC)(H)=PSiMe3 5 could be synthesized and structurally characterized. DFT studies confirmed that the Si=P bond in 2 and 4 is mostly zwitterionic with drastically decreased double-bond character.

Original languageEnglish
Pages (from-to)15060-15063
Number of pages4
JournalAngewandte Chemie-International Edition
Volume54
Issue number50
DOIs
Publication statusPublished - 7 Dec 2015

Keywords

  • heavier olefin analogues
  • multiple bonds
  • phosphorus
  • silicon
  • zwitterions
  • HALF-PARENT PHOSPHASILENE
  • X-RAY-STRUCTURE
  • SILICON-PHOSPHORUS
  • ZWITTERIONIC PHOSPHASILENE
  • UNUSUAL REACTIVITY
  • DOUBLE-BONDS
  • SI-P
  • COMPLEXES
  • PHOSPHANES
  • CHEMISTRY

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