荧光
光化学
可见光谱
堆积
荧光团
材料科学
分子内力
化学
光电子学
光学
物理
有机化学
立体化学
作者
Zhiyuan Han,Meixia He,Wei Wang,Jean‐Marie Lehn,Quan Li
标识
DOI:10.1002/anie.202416363
摘要
Developing visible‐light‐driven fluorescent photoswitches in solid state remains an enormous challenge in smart materials. Such photoswitches are obtained from salicylaldimines through excited‐state intramolecular proton transfer (ESIPT) and subsequent cis‐trans isomerization strategies. By incorporating a bulky naphthalimide fluorophore into Schiff base, three photoswitches achieve dual‐mode changes (both color and fluorescence) in the solid state. In particular, the optimal one generates triple fluorescence changing from green, to yellow and finally orange upon visible light irradiation. This switching process is fully reversible and can be repeated at least 10 times without obvious attenuation, suggesting its superior photo‐fatigue resistance. Mechanism studies reveal that naphthalimide group not only enables the tuning of multicolor with an additional emission, but also induces a folded structure, reducing molecular stacking and facilitating ESIPT and cis‐trans isomerization. As such, photopatterning, ternary encoding and transient information recording and erasing are successfully developed. The present study provides a reliable strategy for visible‐light‐driven fluorescent photoswitches, showing implications for advanced information encryption materials.
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