Acquiring High‐Performance Deep‐Blue OLED Emitters through an Unexpected Blueshift Color‐Tuning Effect Induced by Electron‐Donating ‐OMe Substituents

Abstract

A series of blue-emissive 7-(diphenylamino)-4-phenoxycoumarin derivatives bearing -CF₃ , -OMe, or -N(Me)₂ substituents on the phenoxy subunit were synthesized. Although both the -CF₃ and -N(Me)₂ modifications were found to trigger redshifted fluorescence, the -OMe substitution was demonstrated to exert an unexpected blueshift color-tuning effect toward the deep-blue region. The reason is that the moderate electron-donating -OMe group can endow coumarins with unaltered HOMO but elevated LUMO energy levels. Moreover, the -OMe substitution was found to be beneficial to the thermal stability of these coumarins. Therefore, the trimethoxy-substituted objective compound can act as a high-performance deep-blue organic light-emitting diode (OLED) emitter, and OLED based on it emits deep-blue light with CIE coordinates of (0.148, 0.084), maximum luminance of 7800 cd m^-2 , and maximum external quantum efficiency of 5.1 %. These results not only shed light on the molecular design strategy for high-performance deep-blue OLED emitters through color-tuning, but also show the perspective of coumarin derivatives as deep-blue OLED emitters.