A series of iridium complexes equipped with inert shields: Highly efficient bluish green emitters with reduced self-quenching effect in solid state

In this paper, we synthesize a series of cyclometalated ligands and their corresponding Ir(III) complexes using pentane-2,4-dione as the auxiliary ligand. We discuss the photophysical properties of these Ir(III) complexes in detail, including their UV–Vis absorption spectra, photoluminescence spectra in solid and liquid states, luminescence decay lifetimes, and luminescence quantum yields. The correlation between self-quenching effect and molecular structure is also investigated. It is found that these Ir(III) complexes are solid-emitting ones due to their reduced self-quenching in solid state. Theoretical calculation and experimental data reveal that the following two reasons should be responsible for the reduced self-quenching in solid state: (1) pentane-2,4-dione, phenyl, and triphenylamine moieties serve as inert shields for the excited state Ir(III) complexes; (2) the radiative decay process in these Ir(III) complexes is accelerated by the introduction of electron-donors, and thus partly immune from self-quenching caused by intermolecular action.

The serious phosphorescence self-quenching in solid state is largely and effectively reduced with the help of inert shields, and we successfully realize a series of solid-emitting Ir(III) complexes.Figure optionsDownload as PowerPoint slide