Related Experiment Video
Updated: May 29, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Conjugated asymmetric donor-substituted 1,3,5-triazines: new host materials for blue phosphorescent organic
Zhong-Fu An1, Run-Feng Chen, Jun Yin
1Key Laboratory for Organic Electronics & Information Displays (KLOEID) and Institute of Advanced Materials (IAM), Nanjing University of Posts and Telecommunications (NUPT), 9 Wenyuan Road, Nanjing 210046, PR China.
Abstract:
Conjugated asymmetric donor-substituted 1,3,5-triazines (ADTs) have been synthesized by nucleophilic substitution of organolithium catalyzed by [Pd(PPh(3))(4)]. Theoretical and experimental investigations show that ADTs possess high solubility and thermostability, high fluorescent quantum yield (35%), low HOMO (-6.0 eV) and LUMO (-2.8 eV), and high triplet energy (E(T), 3.0 eV) according to the different substitution pattern of triazine. The application as host materials for blue PHOLEDs yielded a maximum current efficiency of 20.9 cd A(-1), a maximum external quantum efficiency of 9.8%, and a brightness of 9671 cd m(-2) at 5.4 V, making ADTs good candidates for optoelectronic devices.
Related Concept Videos
Photoluminescence: Applications
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Variables Affecting Phosphorescence and Fluorescence

