Syntheses, photoluminescence and electroluminescence of four heteroleptic iridium complexes with 2-(5-phenyl-l,3,4-oxadiazol-2-yl)-phenol derivatives as ancillary ligands

摘要

Four new iridium(III) cyclometalated complexes (Ir1—Ir4) with 4-trifluoromethylphenylpyridine as the main ligand and 2-(5-phenyl-l,3,4-oxadiazol-2-yl)-phenol and its fluoro/trifluoromethyl substituted derivatives as ancillary ligands have been developed. All complexes are green phosphors (λ_(max) = 519-537 nm) with photoluminescence quantum efficiency yields of 10-53% in CH2Cl2 solutions at room temperature, respectively. The organic light emitting diodes (OLEDs) with the structure of ITO/TAPC (l,l-bis[4-(di-p-tolylamino)phenyl]cyclohexane, 60 nm)/lr complexes (8 wt%):SimCP2 (bis[3,5-di(9H-carbazol-9-yl) phenyl] diphenylsilane, 30 nm)/TPBi (1,3,5-tri(l-phenyl-1H-benzo[d]imidazol-2-yl)phenyl, 90 nm)/LiF (1 nm)/Al (100 nm) show good performances. In particular, device G4 based on complex Ir4 (2-(5-pentafluorophenyl-l,3,4-oxadiazol-2-yl)-phenol as ancillary ligand) showed superior performances with a peak current efficiency (η_n of 70.48 cd A~(-1) and a peak external quantum efficiency (η_(ext). EQE) of 19.7%. This study demonstrates that the ancillary ligand attached with the 1,3,4-oxadiazole group could facilitate charge trapping across the bulk of the device for efficient OLEDs.