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Updated: Mar 12, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Highly Luminescent π-Conjugated Terpyridine Derivatives Exhibiting Thermally Activated Delayed Fluorescence
Hisahiro Sasabe1,2, Yuya Hayasaka1,2, Ryutaro Komatsu1,2
1Department of Organic Materials Science, Graduate School of Organic Materials Science, Yamagata University, 4-3-16 Jonan, Yonezawa, Yamagata, 992-8510, Japan.
Abstract:
Typically, luminescent π-conjugated 2,2':6',2''-terpyridine (tpy) derivatives are versatile components for tridentate metal ligands, supramolecular materials, two-photon absorption bioimaging probes, fluorescent ion sensors, and organic light-emitting devices. However, a limited number of luminescent tpy materials, other than metal complexes, have been reported. This study introduces a series of π-conjugated tpy derivatives that exhibit strong thermally activated delayed fluorescence (TADF). We have observed that a blue tpy emitter outperforms conventional fluorescent emitters. Additionally, a green tpy emitter has exhibited a performance that is almost comparable to that of its green phosphorescent counterparts, realizing an external quantum efficiency close to 25 % and a power efficiency exceeding 80 lm W-1 with an exceptionally low efficiency roll-off. This study demonstrates the first example of highly luminescent tpy-based TADF emitters.
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