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Updated: May 6, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
A Multiresonant Thermally Activated Delayed Fluorescent Dendrimer with Intramolecular Energy Transfer: Application
Sen Wu1, Dongyang Chen1,2, Xiao-Hong Zhang2,3
1Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.
Abstract:
The development of narrowband emissive, bright, and stable solution-processed organic light-emitting diodes (SP-OLEDs) remains a challenge. Here, a strategy is presented that merges within a single emitter a TADF sensitizer responsible for exciton harvesting and an MR-TADF motif that provides bright and narrowband emission. This emitter design also shows strong resistance to aggregate formation and aggregation-cause quenching. It is based on a known MR-TADF emitter DtBuCzB with a donor-acceptor TADF moiety consisting of either tert-butylcarbazole donors (tBuCzCO2HDCzB) or second-generation carbazole-based donor dendrons (2GtBuCzCO2HDCzB) and a benzoate acceptor. The TADF moiety acts as an exciton harvesting antenna and transfers these excitons via Förster resonance energy transfer to the MR-TADF emissive core. The SP-OLEDs with 2GtBuCzCO2HDCzB and tBuCzCO2HDCzB thus show very high maximum external quantum efficiencies (EQEmax of 27.9 and 22.0%) and minimal efficiency roll-off out to 5000 cd m-2.

