发光
激发态
聚合物
分子
配体(生物化学)
配位聚合物
材料科学
光化学
化学物理
化学
结晶学
光电子学
原子物理学
物理
有机化学
复合材料
受体
生物化学
作者
Zheng Wang,Cheng‐Yi Zhu,Jun‐Ting Mo,Xian‐Yan Xu,Jia Ruan,Mei Pan,Cheng‐Yong Su
标识
DOI:10.1002/anie.202012831
摘要
Abstract Materials with tunable long persistent luminescence (LPL) properties have wide applications in security signs, anti‐counterfeiting, data encrypting, and other fields. However, the majority of reported tunable LPL materials are pure organic molecules or polymers. Herein, a series of metal‐organic coordination polymers displaying color‐tunable LPL were synthesized by the self‐assembly of HTzPTpy ligand with different cadmium halides (X=Cl, Br, and I). In the solid state, their LPL emission colors can be tuned by the time‐evolution, as well as excitation and temperature variation, realizing multi‐mode dynamic color tuning from green to yellow or green to red, and are the first such examples in single‐component coordination polymer materials. Single‐crystal X‐ray diffraction analysis and theoretical calculations reveal that the modification of LPL is due to the balanced action from single molecule and aggregate triplet excited states caused by an external heavy‐atom effect. The results show that the rational introduction of different halide anions into coordination polymers can realize multi‐color LPL.
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