Title Crystal-state quad-mode triplet emissions of D-A-A '-AIEE and visible-light-excited persistent phosphorescence
Authors Liu, Jianwei
Ma, Zhimin
Li, Zewei
Liu, Yan
Fu, Xiaohua
Jiang, Hong
Ma, Zhiyong
Jia, Xinru
Affiliation Beijing Univ Chem Technol, Coll Chem Engn, Beijing State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
Natl High Tech Ind Dev Zone Jingdezhen, Jingdezhen 333000, Peoples R China
Peking Univ, Minist Educ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci,Key Lab Polymer Chem & P, Beijing 100871, Peoples R China
Issue Date Apr-2021
Publisher DYES AND PIGMENTS
Abstract Herein, we succeed in finding crystal-state quad-mode triplet emissions through the concept of integration of thermally activated exciton release from T-1* and introducing intramolecular electron coupling. Two new D-A-A'D type carbazol-nicotinamide isomers (P1 and P2) with the pyridine ring as the core are synthesized. The crowded D-A-A'-D structure makes P1 and P2 in a highly twisted state, which is conducive to lowering the Delta E-ST and E-TD. Excitingly, P1 and P2 achieve the crystal-state quad-mode triplet emissions, including ultralong room temperature phosphorescence from T-1*, TADP from T-1 via thermally activated exciton release (TAER), the original molecular phosphorescence from T-1 and TADF from S-1 via TAER and reverse intersystem crossing (RISC). Especially, the long-lived emissions of P1 have a rather high quantum yield of 34.3%. The intramolecular electron coupling is observed in the single crystal, verifying the original T-1 phosphorescence. The Delta E-ST and E-TD of the crystals can be calculated experimentally to be 0.19/0.18 eV and 0.19/0.20 eV, respectively, for P1 and P2. And the TAER and RISC process is validated by temperature-dependent experiment. Besides, the P2 crystals manifest fascianting visible-light-excited persistent phosphorescence and P1 shows remarkable AIEE property. To the best of our knowledge, it is the first time to find crystal-state quad-mode triplet emissions at mom temperature experimentally. This study is a breakthrough in the development of multi-mode phosphorescence mechanism.
URI http://hdl.handle.net/20.500.11897/609377
ISSN 0143-7208
DOI 10.1016/j.dyepig.2021.109178
Indexed SCI(E)
Appears in Collections: 化学与分子工程学院
高分子化学与物理教育部重点实验室

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