Reaction of [M(CO)4]- (M = Ir, Rh) with cyclopropenyl tetrafluoroborate - Ring opening and coupling of cyclopropenyl ligands to form dinuclear metal complexes

Pek Ke Chan, Weng Kee Leong*

*Corresponding author for this work

Research output: Contribution to journalShort surveypeer-review

1 Citation (Scopus)

Abstract

Reaction of the iridium tetracarbonylate [PPN][Ir(CO)4] (1a) with triphenylcyclopropenyl tetrafluoroborate [C3Ph3][BF4] afforded two dinuclear species Ir2(CO)4(μ,η12- C3Ph3)(μ,η23 -C3Ph3) (2) and Ir2(CO)4(μ,η44- C6Ph6) (3a) resulting from the ring opening and in the latter case, coupling of the resulting acyclic, propenyl ligands. The analogous reaction with [PPN][Rh(CO)4] (1b) afforded only the rhodium analogue for 3a.

Original languageEnglish
Pages (from-to)2641-2644
Number of pages4
JournalJournal of Organometallic Chemistry
Volume693
Issue number15
DOIs
Publication statusPublished - Jul 15 2008
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

Keywords

  • C-C coupling
  • Cyclopropenyl
  • Diiridium
  • Ring opening

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