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Iridium(III) complexes have attracted considerable attention owing to their outstanding photophysical properties, making them promising candidates for optoelectronic devices, bioimaging, and oxygen sensing. In this work, heteroleptic Ir(III) complexes containing 2-(2,4-difluorophenyl)pyridine (fppy) as cyclometalating ligands and PIB, PIB-CH₃, and PIB-4F as ancillary phenylimidazole–phenanthroline derivatives were synthesized and characterized by FTIR, ¹H, ¹³C, and ¹⁹F NMR, COSY, NOESY, HSQC, and high-resolution ESI-TOF mass spectrometry. Photophysical studies were performed in 1.0 × 10⁻⁵ mol L⁻¹ solutions using UV–Vis absorption, excitation, emission, photoluminescence quantum yield, and excited-state lifetime measurements under aerated and nitrogen-saturated conditions. The complexes exhibited intense ligand-centered absorption bands between 270–280 nm and broad emission centered at approximately 510 nm, characteristic of mixed ³LC/³MLCT excited states. Nitrogen saturation increased the photoluminescence quantum yield from approximately 1% to 5%, confirming oxygen-responsive phosphorescence and highlighting the potential of these complexes for future oxygen-sensing applications.
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