Acta Crystallographica Section E (Jan 2010)

mer-Bis[3,5-difluoro-2-(2-pyridyl)phenyl-κ2C1,N]{5-(2-pyridyl-κN)-3-[3-(4-vinylbenzyloxy)phenyl]-1,2,4-triazol-1-ido}iridium(III) methanol solvate

  • Peter G. Jones,
  • Marc Debeaux,
  • Andreas Weinkauf,
  • Henning Hopf,
  • Wolfgang Kowalsky,
  • Hans-Hermann Johannes

DOI
https://doi.org/10.1107/S1600536809052726
Journal volume & issue
Vol. 66, no. 1
pp. m66 – m67

Abstract

Read online

In the title compound, [Ir(C11H6F2N)2(C22H17N4O)]·CH3OH, the coordination at iridium is essentially octahedral, but with distortions associated with the bite angles of the ligands [76.25 (9)–80.71 (12)°] and the differing trans influences of C and N ligands [Ir—N = 2.04 Å (average) trans to N but 2.14 Å trans to C]. All three bidentate ligands have coordinating ring systems that are almost coplanar [interplanar angles = 1.7 (1)–3.8 (2)°]. The vinylbenzyl group is disordered over two positions with occupations of 0.653 (4) and 0.347 (4). The methanol solvent molecule is involved in a classical O—H...N hydrogen bond to a triazole N atom.