分子间力
磷光
系统间交叉
发光
分子
卤键
持续发光
卤素
光化学
纳米技术
磷光有机发光二极管
激子
化学
化学物理
材料科学
光电子学
荧光
单重态
氢键
有机化学
原子物理学
烷基
激发态
物理
热释光
量子力学
作者
Wenbo Dai,Xiaowei Niu,Xinghui Wu,Yue Ren,Yongfeng Zhang,Gengchen Li,Han Su,Yunxiang Lei,Jiawen Xiao,Jianbing Shi,Bin Tong,Zhengxu Cai,Yuping Dong
标识
DOI:10.1002/ange.202200236
摘要
Abstract Monotonous luminescence has always been a major factor limiting the application of organic room‐temperature phosphorescence (RTP) materials. Enhancing and regulating the intermolecular interactions between the host and guest is an effective strategy to achieve excellent phosphorescence performance. In this study, intermolecular halogen bonding (CN⋅⋅⋅Br) was introduced into the host–guest RTP system. The interaction promoted intersystem crossing and stabilized the triplet excitons, thus helping to achieve strong phosphorescence emission. In addition, the weak intermolecular interaction of halogen bonding is sensitive to external stimuli such as heat, mechanical force, and X‐rays. Therefore, the triplet excitons were easily quenched and colorimetric multi‐stimuli responsive behaviors were realized, which greatly enriched the luminescence functionality of the RTP materials. This method provides a new platform for the future design of responsive RTP materials based on weak intermolecular interactions between the host and guest molecules.
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