4.8 Article

Long-Lived Triplet Charge Separated State and Thermally ActivatedDelayed Fluorescence in a Compact Orthogonal Anthraquinone-Phenothiazine Electron Donor-Acceptor Dyad

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 13, Issue 11, Pages 2533-2539

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.2c00435

Keywords

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Funding

  1. NSFC [U2001222]
  2. State Key Laboratory of Fine Chemicals, Xinjiang University
  3. Department of Education of the Xinjiang Uyghur Autonomous Region
  4. government assignment for FRC Kazan Scientific Center of RAS

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A long-lived and thermally activated triplet charge separated state was observed in a compact electron donor-acceptor dyad. The study results are useful for designing compact electron donor-acceptor dyads with long-lived charge separated states and studying the mechanism of thermally activated delayed fluorescence.
A long-lived triplet charge separated state (3CS state lifetime: 0.56 mu s) wasobserved in acompactelectron donor-acceptor dyad with electron donor phenothiazine (PTZ)and acceptor anthraquinone (AQ) directly connected by a single C-N bond (AQ-PTZ). The1CS state energy (2.0 eV in cyclohexane) is lower than those of the3AQ (2.7 eV) or the3PTZstate (2.6 eV). By oxidation of the PTZ unit, thus increasing of the1CS state energy (2.7 eV incyclohexane), thermally activated delayedfluorescence (TADF) was observed [Tau= 17.7 ns(99.9%)/1.5 mu s (0.1%)]. Time-resolved electron paramagnetic resonance (TREPR) spectraconfirm the electron spin multiplicity of the3CS state, and the zero-field-splitting (ZFS)parameters|D|and|E|are 48.2 mT and 11.2 mT, respectively. These results are useful for designof compact electron donor-acceptor dyads to access the long-lived3CS state and study theTADF mechanism.

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