Synthesis and reactivity of stannyloligosilanes IV [1]: From hydrido substituted stannasilanes towards stannasiloxanes

Ulrich Englich, Ingo Prass, Karin Ruhlandt-Senge, Thorsten Schollmeier, Frank Uhlig

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

Hydrido substituted stannasilanes of the type Z-SnR2-Si(H)R′2 or (R′2Si(H))2SnR2 (Z=H, Me, Ph; R, R′=alkyl, Ph) are accessible by reaction of either alkali metal stannides (MSn(Z)R2; M=Li, Na) with halogen substituted silanes (X-Si(H)R′2; X=F, Cl) or chlorostannanes (R2SnCl2, Ph3SnCl) and fluorosilanes (F-Si(H)R′2) in the presence of magnesium. Stannasilanes with halogen substituents at the silicon as well as the tin atom are formed by treatment of the hydrido substituted stannasilanes with CHCl3 or CCl4. The hydrido substituted stannasilanes decompose in contact with air to distannanes and siloxanes or to the linear (tBu2Sn(-O-tBu2Si-OH) 2) and cyclic ((-tBu2Sn-O-iPr2Si-O-) 2) stannasiloxanes.

Original languageEnglish (US)
Pages (from-to)931-943
Number of pages13
JournalMonatshefte fur Chemie
Volume133
Issue number7
DOIs
StatePublished - Jan 1 2002
Externally publishedYes

Keywords

  • Halogenation
  • Oxidation
  • Stannasilanes
  • X-Ray crystallography

ASJC Scopus subject areas

  • Chemistry(all)

Fingerprint Dive into the research topics of 'Synthesis and reactivity of stannyloligosilanes IV [1]: From hydrido substituted stannasilanes towards stannasiloxanes'. Together they form a unique fingerprint.

  • Cite this