Narrow-emitting pyridoimidazole functionalized N-heterocyclic carbene based tetradentate Pt(II) complexes for blue phosphorescent organic light-emitting diodes

Abstract

Two novel classes of N-heterocyclic carbene (NHC) based tetradentate Pt(II) complexes possessing bulky benzyl groups and pyridoimidazole ligands were designed and synthesized to produce efficient blue phosphorescent organic light-emitting diodes (PHOLEDs). Two blue Pt(II) complexes are reported, namely, platinum (II) [2-(3-(1-(4-(tert-butyl)benzyl)-1H-imidazo [4,5-b]pyridin-3(2H)-yl)phenoxy)-9-(pyridin-2-yl)-9H-carbazole] (Pt(t-BuBnOCzPy)) and platinum (II) [3-(3-(1-benzyl-1H-imidazo [4,5-b]pyridin-3(2H)-yl)phenoxy)-9-(4-(tert-butyl)pyridin-2-yl)-9H-carbazole] (Pt(BnOCz4t-BuPy)), respectively. Notably, pyridoimidazole and bulky benzyl groups efficiently reduced steric hindrance, vibrational peaks, and intermolecular interactions. The photophysical and electrochemical properties of the two Pt(II) complexes were analytically examined experimentally and theoretically. The complexes exhibited blue electroluminescence (EL) emission at 466 nm with a small full-width half maximum (FWHM) of 26 nm and completely suppressed vibrational emission peaks. Blue PHOLEDs, at 5 wt% Pt(t-BuBnOCzPy) and Pt(BnOCz4t-BuPy) doping ratios exhibited maximum external quantum efficiencies (EQEmax) of 19 and 18.6 %, maximum power efficiencies (PEmax) of 25.5 and 24.9 cd m−2, and maximum current efficiencies (CEmax) of 24.3 and 24.3 cd m−2 with Commission International de I'Eclairage (CIEx,y) color coordinates of (0.13, 0.17) and (0.13, 0.17), respectively. These superior results suggest that the designed benzylated NHC pyridoimidazole tetradentate Pt(II) complexes provide a novel means of reducing steric hindrance and intermolecular interactions.