The regioisomeric effect on the excited-state fate leading to room-temperature phosphorescence or thermally activated delayed fluorescence in a dibenzophenazine-cored donor-acceptor-donor system

Exploring the design principle for switching between thermally activated delayed fluorescence (TADF) and room temperature phosphorescence (RTP) is a fundamentally important research to develop triplet-mediated photofunctional organic materials. Herein systematic studies on the regioisomeric and substituent effects in a twisted donor-acceptor-donor (D-A-D) molecular scaffold (A = dibenzo[a,j]phenazine; D = dihydrophenazasiline) on the fate of its excited state have been performed. The study revealed that regioisomerism clearly affects the emission behavior of the D-A-D compounds. Moreover, distinct differences in TADF, dual TADF & RTP, and dual RTP were observed, depending on the host used. Furthermore, organic light-emitting diodes (OLEDs) fabricated with the developed emitters achieved high external quantum efficiencies (EQEs) of up to 7.4% for RTP-based OLEDs.

Automated summary

This study systematically investigated the effects of regioisomerism and substituents on the excited state of a molecular scaffold, and explored the emission behavior of the developed compounds in TADF and RTP. The results showed that the developed emitters achieved high external quantum efficiencies in RTP-based OLEDs.