Long-Lived Emissive Hydrogen-Bonded Macrocycles: Donors Regulating Room-Temperature Phosphorescence and Thermally Activated Delayed Fluorescence

被引:10
|
作者
Ye, Zecong [1 ]
Lian, Mingbing [1 ]
Yang, Zhiyao [2 ]
Fu, Yu [1 ]
Wang, Zhenwen [2 ]
Mu, Yingxiao [1 ]
Ji, Shaomin [1 ]
Zhang, Hao-Li [1 ,3 ]
Yuan, Lihua [2 ]
Chi, Zhenguo [4 ]
Huo, Yanping [1 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
[2] Sichuan Univ, Coll Chem, Chengdu 610064, Peoples R China
[3] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[4] Sun Yat Sen Univ, Sch Chem, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
host-guest complexation; hydrogen-bonded macrocycle; room-temperature phosphorescence; thermally activated delayed fluorescence; white-light emission; LIGHT-EMITTING-DIODES; HIGHLY EFFICIENT; MOLECULAR DESIGN; HOST-GUEST; PHOTOLUMINESCENCE; TRANSITIONS; PERSISTENT;
D O I
10.1002/adom.202202521
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Despite vast applications of macrocycles in supramolecular chemistry, achieving long-lived emissions including room-temperature phosphorescence (RTP) or thermally activated delayed fluorescence (TADF) for potential use still presents a great challenge. This work first reports hydrogen-bonded (H-bonded) macrocycles emitting RTP and TADF by introducing various donors onto the same aramide skeleton containing a rigid acceptor. The formation of charge transfer effectively enhances the photoluminescence efficiency. Aromatic carbonyl groups promote the intersystem crossing. The drastically reduced flexibility of chromophores fixed by the H-bonded macrocyclic framework contributes to suppress the nonradiative decay to stabilize triplet excitons. Therefore, RTP and TADF are acquired by altering donors, and are systematically revealed by comparisons with control compounds and theoretical calculations. Finally, near white-light emission (CIE, 0.30, 0.33) is realized via host-guest interactions.
引用
收藏
页数:11
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