ArticleCommunications chemistry2024
Donor-only substituted benzene achieves thermally activated delayed fluorescence.
Article in Communications chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Merging dynamic and static chirality in propeller-shaped carbazole oligomersRSC advances · 2026Article
- Diindolocarbazole as a Core Structure for Narrow-Emitting and Highly Efficient Blue Organic Light-Emitting Diodes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
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Authors and funding
7 authors.
Funding
Abstract
Thermally activated delayed fluorescence (TADF) is a promising mechanism for harvesting triplet excitons in organic light-emitting diodes (OLEDs). The donor-acceptor (D-A) design is the most conventional strategy for developing efficient TADF emitters. A subsequently emerged approach, known as the multiple resonance (MR) effect, also employs electron-donating and electron-withdrawing functional groups. Thus, developing TADF materials has traditionally relied on ingenuity in selecting and combining two functional units. Here, we have realized a TADF molecule by utilizing only a carbazole donor moiety. This molecule is an unusual example in the family of TADF materials and offers better insight into the electronic structures in the excited states for luminescent materials.
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Registered trials
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