自愈水凝胶
荧光
超分子化学
加密
纳米技术
化学
材料科学
计算机科学
生物系统
高分子化学
结晶学
光学
物理
生物
操作系统
晶体结构
作者
Shihong Wu,Xin Xia,Ronghui Zhou,Ronghui Zhou
出处
期刊:Macromolecules
[American Chemical Society]
日期:2023-07-19
卷期号:56 (15): 5813-5824
被引量:3
标识
DOI:10.1021/acs.macromol.3c00505
摘要
Dynamic time-dependent fluorescent encrypted hydrogels provide a highly secure and sophisticated information security strategy. However, challenges still remain in developing new green encrypted hydrogels with simple preparation. Herein, a new series of guanosine (G)-based supramolecular hydrogels with dynamic time-dependent fluorescence rather than traditional fluorescent materials are exquisitely constructed via a one-pot reaction for the first time. Typically, their fluorescence intensity and wavelength can gradually change with the time dimension of more than 1 year, showing promising potential in information encryption–decryption–destruction. A detailed timescale structure characterization combined with the transition-state analysis of the self-assembly process revealed that the G-quartet-based self-assembly in hydrogels has significant endogenous dynamics, which further affects gelation and time-dependent fluorescence through the self-assembly rate. Further combined with the excellent shear thinning, self-healing, and metal ion response properties, the writing, storage, reading, and ″burning after reading″ of information can be successfully realized in a long-term dimension. Therefore, this study illustrates that the ingenious use of functional supramolecular self-assembly building blocks will be a useful strategy for the development of dynamic time-dependent fluorescent encrypted hydrogels.
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