智能材料
执行机构
荧光
光子
材料科学
代表(政治)
爆炸物
纳米技术
聚合物
烯烃纤维
配体(生物化学)
工作(物理)
环加成
聚合
光电子学
双光子激发显微术
光子学
光诱导电子转移
三维光学数据存储
化学
物理
计算机科学
智能聚合物
对偶(语法数字)
纳米复合材料
分子机器
作者
Ling Xin,Yuehua Chen,Jia‐Qi Pan,Bin Tan,Jie Zhang
摘要
By leveraging the dual photochemical activity of vinylpyridinium building blocks, the concurrent [2+2] photocycloaddition and photoinduced electron transfer are integrated within coordination polymer frameworks to achieve triple photoresponses, simultaneously generating photochromism, fluorescence modulation, and photomechanical actuation within a single crystalline system. The efficient photocycloaddition occurs in the interpenetrated framework despite the criss-crossed olefin arrangement, resulting in rapid stress accumulation and release that manifests as explosive photosalient behavior alongside optical switching. The framework-dependent ligand conformations produce distinct fluorescence readouts, allowing the progress of the cycloaddition to be monitored optically. When embedded in poly(vinyl alcohol) matrices, the crystal-level micro-strain is amplified into programmable macroscopic motions including straightening, crawling, and gathering under single-wavelength irradiation. This work provides a design strategy for integrating multiple photoresponses into a single material, contributing to programmable light-driven actuators and adaptive devices.
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