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

作者：Jiang, Yu-Ying; Liu, Hui; Li, Ting; Zhang, Kun; Gao, Peng-Fu; Zhou, Meng-Shu; Zhang, Li-Lei^*; Fu, Hong-Ru^*

来源：Crystal Growth and Design, 2022, 22(4): 2725-2732.

DOI：10.1021/acs.cgd.2c00113

• TRIPLET EXCITED-STATES
• DELAYED FLUORESCENCE
• CHARGE-TRANSFER
• POPULATION

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.