Theoretical perspective on electronic structure and photophysical properties for three cyclometalated iridium(III) complexes bearing different substituent groups on the main ligands

Abstract

To investigate the influence of the different substituents in the main ligands on the electronic structures, phosphorescent properties, and organic light-emitting devices (OLEDs) performance, three iridium(III) complexes 1, 2, and 3 are studied by means of the density functional theory/time-dependent density functional theory (DFT/TDDFT). Ionization potential, electron affinities, and reorganization energy have also been obtained to evaluate the charge transfer and balance properties between hole and electron for the three complexes. The lowest energy absorption wavelength calculated for complex 1 is in very good agreement with the experimental value. The lowest energy emissions of complexes 1, 2, and 3 are localised at 492, 565, and 510 nm, respectively, at M052X level. It is expected that this work might provide a way to develop potential iridium(III) phosphors with good electroluminescent performance.