Coordination-Induced Approach of a Carbazole-Based Molecule to Modulate Packing Modes for Ultralong Room-Temperature Phosphorescence

被引:7
|
作者
Jiang, Yu-Ying [1 ,2 ]
Liu, Hui [1 ,2 ]
Li, Ting [2 ]
Zhang, Kun [1 ,2 ]
Gao, Peng-Fu [2 ]
Zhou, Meng-Shu [2 ]
Zhang, Li-Lei [2 ]
Fu, Hong-Ru [1 ,2 ]
机构
[1] China Three Gorges Univ, Coll Mat & Chem Engn, Yichang 443002, Peoples R China
[2] Luoyang Normal Univ, Coll Chem & Chem Engn, Luoyang 471934, Peoples R China
基金
中国国家自然科学基金;
关键词
TRIPLET EXCITED-STATES; DELAYED FLUORESCENCE; CHARGE-TRANSFER; POPULATION;
D O I
10.1021/acs.cgd.2c00113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlling molecular packing is important to modulate the aggregate states and the optoelectronic characteristics. Here, we employ a coordination-driven self-assembly, two coordination polymers, [Cd-2(CzIP)(2)(DMPU)(2)] (1) and [Cd-2(CzIP)(2)(mu O3-)(H2O)(2)] (2) (CzIP = 5-(9H- carbazol-9-yl)-isophthalic acid, DMPU = N,N-dimethylpropyleneurea), were successfully synthesized. These two compounds exhibit a molecular packing-dependent emission. Compound 1, where CzIP molecules feature the monomer packing mode, exhibits dual emission, including blue fluorescence and ultralong phosphorescence at room temperature (RTP). The phosphorescence lifetime of compound 1 is 0.63 s at 553 nm under ambient conditions. However, compound 2 shows excimer-dominated green fluorescence emission without RTP. Importantly, it is demonstrated that the coordination-induced pattern opens a way for the development of organic optoelectronic properties by regulating the molecular packing modes.
引用
收藏
页码:2725 / 2732
页数:8
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