磷光
共价键
聚合物
环氧树脂
材料科学
光激发
光化学
猝灭(荧光)
化学工程
高分子化学
纳米技术
化学
荧光
有机化学
复合材料
激发
物理
量子力学
电气工程
工程类
作者
Zihan Zhao,Pei‐Chen Zhao,Shi‐Yi Chen,You‐Xuan Zheng,Jing‐Lin Zuo,Cheng‐Hui Li
标识
DOI:10.1002/anie.202301993
摘要
Room-temperature phosphorescence (RTP) polymers, whose emission can persist for a long period after photoexcitation, are of great importance for practical applications. Herein, dynamic covalent boronic ester linkages with internal B-N coordination are incorporated into a commercial epoxy matrix. The reversible dissociation of B-N bonds upon loading provides an efficient energy dissipation pathway for the epoxy network, while the rigid epoxy matrix can inhibit the quenching of triplet excitons in boronic esters. The obtained polymers exhibit enhanced mechanical toughness (12.26 MJ m-3 ), ultralong RTP (τ=540.4 ms), and shape memory behavior. Notably, there is no apparent decrease in the RTP property upon prolonged immersion in various solvents because the networks are robust. Moreover, the dynamic bonds endow the polymers with superior reprocessablity and recyclability. These novel properties have led to their potential application for information encryption and anti-counterfeiting.
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