偶氮苯
自愈水凝胶
发光
离解(化学)
异构化
化学
镧系元素
相变
光化学
组合化学
材料科学
高分子化学
离子
分子
有机化学
催化作用
物理
量子力学
光电子学
作者
Zhiqiang Li,Guannan Wang,Yige Wang,Huanrong Li
标识
DOI:10.1002/anie.201712670
摘要
Abstract We report herein on remote control over a reversible phase transition of robust luminescent hybrid hydrogels as enabled by the rational selection and incorporation of photoswitches. Azobenzene units functionalized with a guanidinium group were utilized as the photoswitches and incorporated through a host–guest inclusion method involving α‐cyclodextrins functionalized with 2,6‐pyridinedicarboxylic acid (PDA) groups. While the guanidinium functional groups bind to the negatively charged Laponite matrix surface to connect organic and inorganic components, the PDA groups enable simultaneous coordination with different lanthanide metal ions, thus rendering the hydrogel broadly luminescent. Owing to its conformation‐dependent binding behavior with α‐cyclodextrin, the isomerization of azobenzene induced association or dissociation of the inclusion complexes and thus lead to a reversible photocontrolled sol↔gel phase transition of the luminescent hybrid hydrogels.
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