Naphthalimide‐Conjugated Spiropyran: Dual‐State Emission and Photo‐Responsive Dynamic Fluorescence Color for Information Encryption Application
Source abstract
Abstract
Abstract Developing photo‐switch molecules that show fluorescence in both monomeric and aggregated states, with light‐controllable fluorescence wavelength is far‐reaching and a great challenge. Spiropyran (SP) has received considerable attention in this field. Herein, by conjugating naphthalimide to the indole moiety of SP, a new spiropyran derivative, named NMI‐SP is obtained. NMI‐SP shows dual‐state emission with excellent fluorescence in both its monomeric and aggregated states, attributed to the intramolecular charge transfer character. Moreover, NMI‐SP demonstrates obvious photochromic behavior, accompanied by the visible color change from yellow to green in THF solution, and photo‐responsive fluorescence color change from orange to red in the aggregated state. This work provides new insights into the design of photo‐responsive materials based on SP fluorophore and highlights their potential applications in digital coding and information conversion.
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Research context
OpenAlex topics: Photochromic and Fluorescence Chemistry · Photoreceptor and optogenetics research · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China
Beijing Key Laboratory of Special Elastomer Composite Materials College of New Materials and Chemical Engineering Beijing Institute of Petrochemical Technology Beijing 102617 P. R. China
Funding
National Natural Science Foundation of China
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