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Do carbyne radicals really exist in aqueous solution?

  • Benny Bogoslavsky
  • , Ophir Levy
  • , Anna Kotlyar
  • , Miri Salem
  • , Faina Gelman
  • , Avi Bino*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

They do exist! Free carbyne radicals can be prepared at room temperature in an aqueous solution by the decomposition of mono- or trinuclear metal (M) complexes containing alkylidyne ligands (see scheme; red C, blue M, green H). The generated radicals then react to form a variety of organic compounds by chain-lengthening reactions in solution. They also exhibit hydrogen, oxygen, or carbon abstraction from solvent, reactant, or product molecules.

Original languageEnglish
Pages (from-to)90-94
Number of pages5
JournalAngewandte Chemie - International Edition
Volume51
Issue number1
DOIs
StatePublished - 2 Jan 2012

Keywords

  • C-C coupling
  • alkynes
  • carbynes
  • molybdenum
  • radicals

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