Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1235822 | Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | 2012 | 7 Pages |
Phosphorescent studies of 2-arylimidazole heteroleptic cyclometalated iridium(III) complexes with picolinic acid as the ancillary ligand were made. The observed experimental data reveal that these complexes possess dominantly 3MLCT and 3π–π* excited states and the solvent shift of these complexes is interpreted by Reichardt–Dimroth and Marcus solvent functions. The results are consistent with prior assignments on the absorption band to a metal-to-ligand charge transfer excited state associated with chelating ligand. Emission kinetic studies exploited that the radiative transition (kr) increases with increasing λem.
Graphical abstractSynthesis of heteroleptic iridium complex.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Bands located at longer wavelength assigned to 1MLCT ← S0 and 3MLCT ← S0 transitions. ► 3MLCT ← S0 is allowed by mixing of spin–orbit coupling. ► 3MLCT ← S0 is close to 1MLCT ← S0. ► Mixing of excited states (LC and MLCT). ► (1E1 − 3E1) increases with decrease in λem, hence, kr increases with increase in λem.