A mixed chloride/trifluoromethanesulfonate ligand species in a ruthenium(II) complex

Acta Crystallogr C. 2013 Aug;69(Pt 8):859-61. doi: 10.1107/S0108270113019057. Epub 2013 Jul 20.

Abstract

The compound [2-(aminomethyl)pyridine-κ²N,N'][chlorido/trifluoromethanesulfonato(0.91/0.09)][(10,11-η)-5H-dibenzo[a,d]cyclohepten-5-amine-κN](triphenylphosphane-κP)ruthenium(II) trifluoromethanesulfonate dichloromethane 0.91-solvate, [Ru(CF₃SO₃)0.09Cl0.91(C₆H₈N₂)(C₁₅H₁₃N)(C₁₈H₁₅P)]CF₃SO₃·0.91CH₂Cl₂, belongs to a series of RuII complexes that had been tested for transfer hydrogenation, hydrogenation of polar bonds and catalytic transfer hydrogenation. The crystal structure determination of this complex revealed disorder in the form of two different anionic ligands sharing the same coordination site, which other spectroscopic methods failed to characterize. The reduced catalytic activity of the title compound was not fully understood until the crystallographic data provided evidence for the mixed ligand species. The crystal structure clearly shows that the majority of the synthesized material has a chloride ligand present. Only a small portion of the material is the expected complex [RuII(OTf)(ampy)(η²-tropNH₂)(PPh₃)]OTf, where OTf is triflate or trifluoromethanesulfonate, ampy is 2-(aminomethyl)pyridine and tropNH₂ is 5H-dibenzo[a,d]cyclohepten-5-amine.

Keywords: crystal structure; mixed anionic ligands; non-innocent co-operative ligands; ruthenium(II) complexes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / chemistry*
  • Crystallography, X-Ray
  • Ligands
  • Mesylates / chemistry*
  • Models, Molecular
  • Pyridines / chemical synthesis*
  • Pyridines / chemistry
  • Ruthenium / chemistry*

Substances

  • Coordination Complexes
  • Ligands
  • Mesylates
  • Pyridines
  • Ruthenium
  • trifluoromethanesulfonic acid