详细信息

Emission-Tunable Room-Temperature Phosphorescent Two-Dimensional Polymer Network via a Photo-Cross-Linking Reaction  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Emission-Tunable Room-Temperature Phosphorescent Two-Dimensional Polymer Network via a Photo-Cross-Linking Reaction

作者:Lin, Xiaohan[1,2];Xu, Chen[1,2];Qiu, Yiyang[3];Ma, Xiang[1,2]

机构:[1]East China Univ Sci & Technol, Key Lab Adv Mat, Sch Chem & Mol Engn, Inst Fine Chem, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Feringa Nobel Prize Scientist Joint Res Ctr, Sch Chem & Mol Engn, Frontiers Sci Ctr Mat & Dynam Chem,Inst Fine Chem, Shanghai 200237, Peoples R China;[3]Xuhui High Sch, Shanghai 200030, Peoples R China

年份:2023

卷号:62

期号:33

起止页码:13053

外文期刊名:INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH

收录:;EI(收录号:20233614668172);WOS:【SCI-EXPANDED(收录号:WOS:001045195300001)】;

基金:The authors gratefully acknowledge financial support from the National Key Research and Development Program of China (2022yfb32033500), National Science Foundation of China (22125803 and 22020102006), Program of Shanghai Academic/Technology Research Leader (20XD1421300), and Fundamental Research Funds for the Central Universities.

语种:英文

外文关键词:Crosslinking - Phosphorescence

摘要:Pure organic room-temperature phosphorescent materials have been widely used in optical materials, materiobiology, and sensing devices in recent years due to their long-lifetime emission and low production costs. Room-temperature phosphorescent polymers with dynamic and controllable properties have rich extensibility, and they are becoming the new favorite of intelligent luminescent materials. In this work, a dynamic covalent bond was introduced into an amorphous polymer with room-temperature phosphorescent properties. The polymers were modified by a [2 + 2] photocyclization reaction. After photoreaction, not only did the luminescent color of the polymer change, but also the morphology of the polymer changed from a linear structure to a two-dimensional network structure, and the phosphorescence quantum yields and lifetimes of the polymers were significantly improved. This research provides a new idea for the design and development of controllable smart room-temperature phosphorescent materials.

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