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Updated: Apr 22, 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 and Photophysical Properties of Tetra-Aryl-Substituted 2H-benzo[d][1,2,3]triazole Derivatives with
1College of Agriculture & Biotechnology, Zhejiang University, Hangzhou, P. R. China.
Abstract:
Dual-state emission (DSE) molecules, which fluoresce efficiently both in dilute solution and aggregated state, bridge the limitations of aggregation induced emission (AIE) and aggregation caused quenching (ACQ) systems and therefore hold exceptional promise for next-generation luminescent materials. In this study, a series of new fluorescent compounds (1-4) based on 2H-benzo[d][1,2,3]triazole were designed and synthesized, and their photophysical properties were systematically investigated across different states. All four compounds exhibit 100% quantum yields (QY) in toluene and retain QY ≥ 44% in the powder state; notably, compounds 1 and 4 preserve QY above 60% in powder state, unambiguously confirming their DSE characteristics. Moreover, the emission profiles remain highly consistent regardless of solvent or aggregation state. In particular, compound 3 displays CIE1931 chromaticity coordinates of (0.15, 0.07) in all states, approaching the standard blue of (0.14, 0.08). Additionally, reversible mechanochromism was observed for compounds 2 and 4.
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