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Temperature-dependent nuclearity in bis(benzimidazoyl) nickel complexes and their catalysis toward conjugate addition of thiophenols to α,β-enones

  • Way Zen Lee*
  • , Tzu Li Wang
  • , Huan Sheng Tsang
  • , Cheng Yuan Liu
  • , Chien Tien Chen
  • , Ting Shen Kuo
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The nuclearity of two previously prepared nickel complexes, [LNiCl(μ-Cl)]2.2CH3OH (1) and L'NiCh (2) (L - bis(l-methylbenzimidazoyl-2-methyl)amine and L' - bis(l-methylbenzimidazoyl-2- methyl)-10-camphorsulfonamide), was found to be temperature-dependent. Mononuclear [LNi(CH3OH)2Cl]Cl.2H20 (3) and dinuclear [L'NiCl(μ-Cl)]2 (4) were obtained as crystals at -20 °C. It is noteworthy that complex 2 can catalyze the conjugate addition of thiophenols to a,ß-enones in high yields; in contrast, the same reaction catalyzed by NiCl2THF or complex 3 was far less effective.

Original languageEnglish
Pages (from-to)652-655
Number of pages4
JournalOrganometallics
Volume28
Issue number2
DOIs
Publication statusPublished - 2009 Jan 26

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

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