Journal
CHEMICAL COMMUNICATIONS
Volume 52, Issue 12, Pages 2612-2615Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc09645f
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Funding
- Engineering and Physical Sciences Research Council [EP/K016164/1, EP/I006656/1, EP/L02621X/1] Funding Source: researchfish
- EPSRC [EP/K016164/1, EP/L02621X/1, EP/I006656/1] Funding Source: UKRI
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A series of phenothiazine-dibenzothiophene-S, S-dioxide charge-transfer molecules have been synthesized. Increasing steric restriction around the donor-acceptor bond significantly alters contributions from TADF and phosphorescence. Bulky substituents on the 1-(and 9) position(s) of the phenothiazine result in no TADF in the solid state; instead strong phosphorescence is observed at ambient temperature.
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