trans-1,3-pentadiene and cyclobutene complexes of rhodium(I) and iridium(I)

Robert B. Osborne*, James A. Ibers

*Corresponding author for this work

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

The generation of "MClL2" centers in THF solution (M Ir, L AsPh3, SbPh3; M Rh, L SbPh3) leads to stable η2-MCl(C5H8)L2 complexes on the addition of an excess of trans-1,3-pentadiene. For IrCl(PPh3)2, it is only possible to recover a clean pentadiene complex if the reaction is carried out in neat diene solution. Cyclobutene also coordinates to "IrClL2" (L AsPh3, SbPh3) to form an LrCl(C4H6)L2 product when excess cyclobutene is condensed with a starting material at-78°C, THF is added, and the solution is warmed to 25°C. These 16-electron MCl(olefin)L2 complexes are stable to disproportionation after isolation from solution. The most stable complexes are formed with the tertiary arsine and stibine ligands for M Ir.

Original languageEnglish (US)
Pages (from-to)267-272
Number of pages6
JournalJournal of Organometallic Chemistry
Volume232
Issue number3
DOIs
StatePublished - Jun 22 1982

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ASJC Scopus subject areas

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

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