The construction of aggregation-induced charge transfer emission systems in aqueous solution directed by supramolecular strategy

被引:20
|
作者
Qian, Weirui [1 ]
Zuo, Minzan [2 ]
Niu, Pengbo [1 ]
Hu, Xiao-Yu [2 ]
Wang, Leyong [1 ,3 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Jiangsu Key Lab Adv Organ Mat, Nanjing 210023, Peoples R China
[2] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 211106, Peoples R China
[3] Xihua Univ, Dept Chem, Chengdu 610039, Peoples R China
基金
中国国家自然科学基金;
关键词
Aggregation-induced charge transfer emission; Supramolecular strategy; Long luminescence lifetime; Self-assemble; Co-aggregate; ACTIVATED DELAYED FLUORESCENCE; LIGHT-HARVESTING SYSTEM; ORGANIC NANOPARTICLES; EFFICIENT; EXCIPLEX; ENCAPSULATION; TADF;
D O I
10.1016/j.cclet.2021.09.070
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel aggregation-induced charge transfer (CT) emission systems with long luminescence lifetime directed by supramolecular strategy have been successfully developed in water. The dimethylacridine-based electron donor (BrAc) with excellent aggregation ability can co-aggregate with a triazine-based electron acceptor (TRZ) to form nanorods in water, which exhibit CT emission with long lifetime (tau = 0.92 mu s). As for a similar electron donor (QaAc) with poor aggregation ability, water-soluble pillar[5]arene (WP5) can be introduced to promote the aggregation process, leading to the obvious CT emission with long lifetime (tau = 0.61 mu s). In addition, structural modification of the acceptor with substituent groups possessing stronger electron-accepting capabilities will cause red-shift (about 50 nm) of the emission, which allows conveniently constructing long lifetime organic luminescent materials with different emission colors. (C) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页码:1975 / 1978
页数:4
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