The structure of the IrQ(ppy)2 organometallic dual phosphorescent compound was experimentally and theoretically investigated. The Metal-to-Ligand Charge Transfer toward the phenylpiridine and quinoline ligands explains its dual phosphorescence property. The IrQ(ppy)2 organometallic's electronic properties extend the absorption spectra toward the lower energies than Ir(ppy)3 due to the bandgap reduction induced by the quinoline ligand. The magneto-optical measurements reveal A-terms, which are produced by splitting the triplet states and B-terms, which arise when the electronic levels are mixed in the magnetic field. The IrQ(ppy)2 molecule's transport properties confirm an ambipolar character, consisting of a higher hole transport character induced by the phenyilpiridine ligands and a lower electron transport character induced by the quinoline ligand.
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