Tuning of emission: Synthesis, structure and photophysical properties of imidazole, oxazole and thiazole-based iridium (III) complexes

Three new iridium (III) complexes with two cyclometalated C∧N ligands (imidazole, oxazole and thiazole-based, respectively) and one acetylacetone (acac) ancillary ligand have been synthesized and fully characterized. The structure of the thiazole-based complex has been determined by single crystal X-ray diffraction analysis. The Ir center was located in a distorted octahedral environment by three chelating ligands with the N–N in the trans and C–C in the cis configuration. By changing the hetero-atom of C∧N ligands the order S, O and N, a marked and systematic hypsochromic shift of the maximum emission peak of the complexes was realized. The imidazole-based complex emits at a wavelength of 500 nm, which is in the blue to green region. The tuning of emission wavelengths is consistent with the variation of the energy gap estimated from electrochemistry results. An electroluminescent device using the thiazole-based complex as a dopant in the emitting layer has been fabricated. A highly efficient yellow emission with a maximum luminous efficiency of 9.8 cd/A at a current density of 24.2 mA/cm2 and a maximum brightness of 7985 cd/m2 at 19.6 V has been achieved.

Synthesis, structure, electrochemical and photophysical properties of three new iridium complexes with imidazole, oxazole or thiazole-based ligands, respectively, have been reported. The emission wavelength of the complexes can be tuned by about 52 nm by changing the hetero-atom of C∧N ligands.Figure optionsDownload as PowerPoint slide