Theoretical study on the electronic structures and phosphorescent properties of a series of iridium(III) complexes with the different positional N-substitution in the pyridyl moiety

The geometry structures, electronic structures, absorption and phosphorescent properties of a series of iridium(III) complexes with the different N-substitution cyclometalating ligand and the same benzyldiphenylphosphine auxiliary ligand have been theoretically investigated by using the density functional theory method. The lowest energy absorption wavelengths are located at 378nm for A, 430nm for B, 411nm for C, 436nm for D, and 394nm for E. The introduction of N atom substitution at 1-, 2-, 3-, and 4-positions on the pyridyl moiety of complex A leads to an obvious redshifted absorption. The lowest energy emissions for complexes A–E are localized at 450, 409, 438, 483, and 429nm, respectively, simulated in CH2Cl2 medium at M052X level. Ionization potential and electron affinity have been calculated to evaluate the injection abilities of holes and electrons into these complexes. For complex C, the calculated results showed that it can possibly possess the larger radiative decay rate (kr) value than those of other four complexes. It is anticipated that the theoretical studies can provide valuable information for designing new phosphorescent metal complexes of organic light-emitting diodes.