Affiliation:
1. Department of Chemistry Durham University South Road Durham DH1 3LE UK
2. School of Chemistry University of Edinburgh David Brewster Road Edinburgh EH9 3FJ UK
3. Department of Physics Durham University South Road Durham DH1 3LE UK
4. Department of Mathematics, Physics and Electrical Engineering Northumbria University Ellison Place Newcastle upon Tyne NE1 8ST UK
Abstract
AbstractHeterocyclic dimers consisting of combinations of butterfly‐shaped phenothiazine (PTZ) and its chemically oxidized form phenothiazine‐5,5‐dioxide (PTZ(SO2)) have been synthesized. A twist is imposed across the dimers by ortho‐substituents including methyl ethers, sulfides and sulfones. X‐ray crystallography, cyclic voltammetry and optical spectroscopy, underpinned by computational studies, have been employed to study the interplay between the oxidation state, conformational restriction, and emission mechanisms including thermally activated delayed fluorescence (TADF) and room temperature phosphorescence (RTP). While the PTZ(SO2) dimers are simple fluorophores, the presence of PTZ induces triplet‐mediated emission with a mixed PTZ‐PTZ(SO2) dimer displaying concentration dependent hallmarks of both TADF and RTP.
Funder
Engineering and Physical Sciences Research Council
Royal Society of Chemistry
Horizon 2020 Framework Programme
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
3 articles.
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