Reversible Nucleophilic Ring-Opening of Tetraoxapentacene Derivatives: Accessing New Materials for Thermally Activated Delayed Fluorescence

We report the unexpected nucleophilic ring-opening reaction of electron deficient dioxins in the presence of carbazole under basic conditions. This nucleophilic ring-opening reaction is reversible under basic conditions in the absence of nucleophiles. Further, we demonstrate that this unexpected rea...

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Veröffentlicht in:Journal of organic chemistry 2024-11, Vol.89 (21), p.15598-15606
Hauptverfasser: Hiscock, Lana K., Gogoulis, Athan T., Diamantopoulos, Madison, Patel, Vishvam S., Dawe, Louise N., Hudson, Zachary M., Maly, Kenneth E.
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container_end_page 15606
container_issue 21
container_start_page 15598
container_title Journal of organic chemistry
container_volume 89
creator Hiscock, Lana K.
Gogoulis, Athan T.
Diamantopoulos, Madison
Patel, Vishvam S.
Dawe, Louise N.
Hudson, Zachary M.
Maly, Kenneth E.
description We report the unexpected nucleophilic ring-opening reaction of electron deficient dioxins in the presence of carbazole under basic conditions. This nucleophilic ring-opening reaction is reversible under basic conditions in the absence of nucleophiles. Further, we demonstrate that this unexpected reactivity can be used to prepare novel donor–acceptor compounds that are emissive in solution and as thin films and exhibit thermally activated delayed fluorescence (TADF).
doi_str_mv 10.1021/acs.joc.4c01687
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title Reversible Nucleophilic Ring-Opening of Tetraoxapentacene Derivatives: Accessing New Materials for Thermally Activated Delayed Fluorescence
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