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Updated: Feb 27, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Synthesis of 2-(3,5-diarylaminophenyl)-2h-benzo[d][1,2,3]triazoles With Aggregation Induced Emission Properties and
Zhichao Wang1, Xu Wu2, Mingzhi Huang3
1College of Agriculture & Biotechnology, Zhejiang University, Hangzhou, P. R. China.
Abstract:
In this study, a series of new fluorescent compounds (1a-1e) were synthesized based on 2-phenylbenzotriazole acceptor and various diarylamine donors, and their photophysical properties in different states (solution, film, and powder) were investigated. Emissions of 1a-1e cover the spectrum from 413 nm to 572 nm in toluene solutions with various diarylamino donors on 2-phenylbenzotriazole. Among them, 1d and 1e exhibit the classical AIE properties while 1a, 1b and 1c show good emission in both solution and aggregated states. Additionally, all five compounds present large molar absorptivity (> 30000 L·mol-1·cm-1) and excellent emission efficiency. Thus, 2a has a molar absorptivity up to 65,800 L·mol-1·cm-1 in toluene, while 1a shows the emission efficiency up to 79.1%. Besides these, mechanochromic properties were observed for compounds 1a, 1d and 1e, and blue OLEDs were fabricated by using compound 1b or 1c as the active layer.

