The synthesis and isolation of a metal-substituted bis-silene

Dmitry Bravo-Zhivotovskii, Roman Dobrovetsky, Dmitry Nemirovsky, Victoria Molev, Michael Bendikov, Gregory Molev, Mark Botoshansky, Yitzhak Apeloig

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Si, Si: The reaction of bis(lithiosilyl)mercury with R3Si = iPr3Si with two equivalents of 1-adamantoyl chloride gave, by thermal Brook rearrangement, the first metal-substituted bis-silene. The reaction of bis(lithiosilyl)mercury having smaller tBuMe2Si substituents led to a bis(acylsilyl) mercury, which did not rearrange to the bis-silene. The effect of steric congestion on Brook rearrangement was studied computationally. (Chemical Equation Presented)

Original languageEnglish
Pages (from-to)4343-4345
Number of pages3
JournalAngewandte Chemie - International Edition
Volume47
Issue number23
DOIs
Publication statusPublished - May 26 2008

Keywords

  • Anions
  • Lithium
  • Rearrangements
  • Silenes
  • Structure elucidation

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)

Fingerprint Dive into the research topics of 'The synthesis and isolation of a metal-substituted bis-silene'. Together they form a unique fingerprint.

  • Cite this

    Bravo-Zhivotovskii, D., Dobrovetsky, R., Nemirovsky, D., Molev, V., Bendikov, M., Molev, G., Botoshansky, M., & Apeloig, Y. (2008). The synthesis and isolation of a metal-substituted bis-silene. Angewandte Chemie - International Edition, 47(23), 4343-4345. https://doi.org/10.1002/anie.200800973