Isomerization of Internal Alkynes to Iridium(III) Allene Complexes via C-H Bond Activation: Expanded Substrate Scope, and Progress towards a Catalytic Methodology

Molecules. 2015 Nov 10;20(11):20195-205. doi: 10.3390/molecules201119686.

Abstract

The synthesis of a series of allene complexes (POCOP)Ir(η²-RC=(.)=CR') 1b-4b (POCOP = 2,6-bis(di-tert-butylphosphonito)benzene) via isomerization of internal alkynes is reported. We have demonstrated that the application of this methodology is viable for the isomerization of a wide variety of alkyne substrates. Deuterium labeling experiments support our proposed mechanism. The structures of the allene complexes 1b-4b were determined using spectroscopic data analysis. Additionally, the solid-state molecular structure of complex 2b was determined using single crystal X-ray diffraction studies and it confirmed the assignment of an iridium-bound allene isomerization product. The rates of isomerization were measured using NMR techniques over a range of temperatures to allow determination of thermodynamic parameters. Finally, we report a preliminary step towards developing a catalytic methodology; the allene may be liberated from the metal center by exposure of the complex to an atmosphere of carbon monoxide.

Keywords: allenes; crystal structure; iridium; isolation; isomerization; pincer; synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkadienes / chemistry*
  • Alkynes / chemistry*
  • Carbon / chemistry
  • Catalysis
  • Crystallography, X-Ray
  • Iridium / chemistry*
  • Isomerism
  • Models, Molecular
  • Nuclear Magnetic Resonance, Biomolecular
  • Stereoisomerism

Substances

  • Alkadienes
  • Alkynes
  • Iridium
  • propadiene
  • Carbon