Reversible Nucleophilic\nRing-Opening of Tetraoxapentacene\nDerivatives: Accessing New Materials for Thermally Activated Delayed\nFluorescence

We report the unexpected nucleophilic ring-opening reaction\nof\nelectron deficient dioxins in the presence of carbazole under basic\nconditions. This nucleophilic ring-opening reaction is reversible\nunder basic conditions in the absence of nucleophiles. Further, we\ndemonstrate that this unexpected reactivity can be used to prepare\nnovel donor–acceptor compounds that are emissive in solution\nand as thin films and exhibit thermally activated delayed fluorescence\n(TADF).

Publication Details

Journal
Figshare
Published
2024-10-23
DOI
https://doi.org/10.1021/acs.joc.4c01687.s001
Primary Topic
Luminescence and Fluorescent Materials
Type
article
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article

Reversible Nucleophilic\nRing-Opening of Tetraoxapentacene\nDerivatives: Accessing New Materials for Thermally Activated Delayed\nFluorescence

Figshare
Luminescence and Fluorescent Materials
article

Reversible Nucleophilic\nRing-Opening of Tetraoxapentacene\nDerivatives: Accessing New Materials for Thermally Activated Delayed\nFluorescence

article en

Abstract

We report the unexpected nucleophilic ring-opening reaction\nof\nelectron deficient dioxins in the presence of carbazole under basic\nconditions. This nucleophilic ring-opening reaction is reversible\nunder basic conditions in the absence of nucleophiles. Further, we\ndemonstrate that this unexpected reactivity can be used to prepare\nnovel donor–acceptor compounds that are emissive in solution\nand as thin films and exhibit thermally activated delayed fluorescence\n(TADF).

Figshare
Openalex Percentile: Top 76%
Luminescence and Fluorescent Materials
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Reversible Nucleophilic\nRing-Opening of Tetraoxapentacene\nDerivatives: Accessing New Materials for Thermally Activated Delayed\nFluorescence · Figshare (2024) | TGRS Research Map | TGRS