Using substituted cyclometalated quinoxaline ligands to finely tune the luminescence properties of iridium(III) complexes.

Emily E Langdon-Jones, Andrew J Hallett, Jack D Routledge, David A Crole, Benjamin D Ward, James A Platts, Simon J A Pope

School of Chemistry, Main Building, Cardiff University, Park Place, Cardiff CF10 3AT, United Kingdom.

Inorganic chemistry 2013 Jan 7

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The syntheses of five new heteroleptic iridium complexes [Ir(L(1-4))(2)(Diobpy)]PF(6) (where Diobpy = 4,4'-dioctylamido-2,2'-bipyridine) and [Ir(L(3))(2)(bpy)]PF(6) (where L = para-substituted 2,3-diphenylquinoxaline cyclometalating ligands; bpy = 2,2'-bipyridine) are described. The structures of [Ir(L(3))(2)(Diobpy)]PF(6) and [Ir(L(3))(2)(bpy)]PF(6) show that the complexes each adopt a distorted octahedral geometry with the expected trans-N, cis-C arrangement of the cyclometalated ligands. Electrochemical studies confirmed subtle perturbation of the Ir(III/IV) redox couple as a function of ligand variation. Luminescence studies showed the significant contribution of (3)MLCT to the phosphorescent character with predictable and modestly tunable emission wavelengths between 618 and 636 nm. DFT studies provided approximate qualitative descriptions of the HOMO {located over the Ir(5d) center (11-42%) and the phenylquinoxaline ligand (54-87%)} and LUMO {located over the ancillary bipyridine ligands (ca. 93%)} energy levels of the five complexes, confirming significant MLCT character. TD-DFT calculations indicate that UV-vis absorption and subsequent emission has substantial MLCT character, mixed with LLCT. Predicted absorption and emission wavelengths are in good general agreement with the UV-vis and luminescence experiments.

Citation

Emily E Langdon-Jones, Andrew J Hallett, Jack D Routledge, David A Crole, Benjamin D Ward, James A Platts, Simon J A Pope. Using substituted cyclometalated quinoxaline ligands to finely tune the luminescence properties of iridium(III) complexes. Inorganic chemistry. 2013 Jan 7;52(1):448-56