4.6 Article

OBO-Fused Benzo[fg]tetracene as Acceptor With Potential for Thermally Activated Delayed Fluorescence Emitters

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FRONTIERS IN CHEMISTRY
卷 8, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2020.563411

关键词

boron emitters; fluorescence; OLED; TADF; boron

资金

  1. Helmholtz Association Program at the Karlsruhe Institute of Technology
  2. German Research Foundation [SFB1176, CRC1176, 3DMM2O EXC-2082/1-390761711]
  3. Chinese Scholarship Council (CSC)
  4. European Union's Horizon 2020 research and innovation programme under Marie Sklodowska Curie Individual Fellowship (MCIF) [748430-THF-OLED]
  5. Bayrisches Staatsministerium fur Wissenschaft und Kunst (Stmwk)
  6. German Science foundation (DFG) [392306670]
  7. European Union [GA 812872]

向作者/读者索取更多资源

Six luminophores bearing an OBO-fused benzo[fg]tetracene core as an electron acceptor were designed and synthesized. The molecular structures of three molecules (PXZ-OBO, 5PXZ-OBO, 5DMAC-OBO) were determined by single crystal X-ray diffraction studies and revealed significant torsion between the donor moieties and the OBO acceptor with dihedral angles between 75.5 and 86.2 degrees. Photophysical studies demonstrate that blue and deep blue emission can be realized with photoluminescence maxima (lambda(PL)) ranging from 415 to 480 nm in mCP films. The emission energy is modulated by simply varying the strength of the donor heterocycle, the number of donors, and their position relative to the acceptor. Although the DMAC derivatives show negligible delayed emission because of their large singlet-triplet excited state energy difference, Delta E-ST, PXZ-based molecules, especially PXZ-OBO with an experimental Delta E(ST)of 0.25 eV, demonstrate delayed emission in blend mCP films at room temperature, which suggests triplet exciton harvesting occurs in these samples, potentially by thermally activated delayed fluorescence.

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