Interaction of π-bonds of the silicon-silicon triple bond with alkali metals: An isolable anion radical upon reduction of a disilyne

Akira Sekiguchi*, Rei Kinjo, Masaaki Ichinohe

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

32 Citations (Scopus)

Abstract

The reduction of 1,1,4,4-tetrakis[bis(trimethylsilyl)methyl]-1,4-diisopropyltetrasila-2-yne 1 with an equivalent amount of alkali metal (Li, Na, K, KC8) in THF produced the corresponding disilyne anion radicals 2a-c. Their EPR spectra are independent of the metals used in THF, indicating that the disilyne anion radical species exists as solvent-separated ion pairs in polar solvents. The one-electron reduction also occurred with potassium in toluene to produce the potassium salt of the anion radical 3, which was isolated as extremely air- and moisture-sensitive dark brown crystals. The molecular structure of 3 was established by X-ray crystallography, which showed that the potassium ion is solvated by one toluene molecule. The EPR spectrum of 3 in toluene showed the interaction of the anionic silicon atom with the K+ ion.

Original languageEnglish
Pages (from-to)773-775
Number of pages3
JournalSynthetic Metals
Volume159
Issue number9-10
DOIs
Publication statusPublished - May 2009
Externally publishedYes

ASJC Scopus Subject Areas

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics
  • Mechanics of Materials
  • Mechanical Engineering
  • Metals and Alloys
  • Materials Chemistry

Keywords

  • Anion radical
  • Disilyne
  • Reduction
  • Silicon-silicon triple bond
  • X-ray crystallographic analysis

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