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A Comprehensive Survey of Cationic Iridium(III) Complexes Bearing Nontraditional Ligand Chelation Motifs

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume -, Issue 17, Pages 2985-3007

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201300171

Keywords

Iridium; Heterocycles; Luminescence; Electrochemistry; Chelates

Funding

  1. Canadian Foundation for Innovation (CFI)
  2. National Sciences and Engineering Research Council of Canada (NSERC)
  3. Le Fonds Quebecois de la recherche sur la nature et les technologies (FQRNT)
  4. Universite de Sherbrooke
  5. FQRNT

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The useful optoelectronic properties of cationic iridium(III) complexes have been exploited in diverse applications, from visual displays to biological probes to analytical sensors. It is thus not surprising to note the increased recent efforts to document, understand, and ultimately control the photophysical and electrochemical properties of the archetypal cationic iridium(III) complex [(ppy)2Ir(bpy)]+, in which ppyH = 2-phenylpyridine and bpy = 2,2-bipyridine, and decorated versions thereof. Of the ligand architectures explored, the greatest attention has been devoted to ligands that incorporate the common pyridine unit. In this Microreview, we survey the salient emission and electrochemical properties of cationic iridium(III) complexes of the form [(C perpendicular to N)2Ir(L perpendicular to X)]+, in which C perpendicular to N is a cyclometalating ligand and L perpendicular to X is a bidentate neutral ancillary ligand, with at least one heterocyclic ligand other than pyridine. We contrast their properties to that of [(ppy)2Ir(bpy)]+ and highlight recent exploits in materials applications.

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