Source abstract
Abstract
Abstract Emission‐switchable fluorophores often include stimuli‐responsive units in their molecular structures. This strategy works well, but the applicable compounds are limited to the derivatives of several kinds of photochromic molecules such as diarylethene, azobenzene, and spiropyran. Here, this work presents a simple methodology based on a photoresponsive precipitant for achieving color‐switchable photoluminescence. A luminescent dye, cyano‐substituted oligo(phenylenevinylene) (COPV), features both twisted intramolecular charge transfer and aggregation‐induced emission shift properties, leading to the change in the luminescence color from green to red upon precipitation. The COPV, together with photoisomerizable precipitant azobenzene (C6), is doped into spherical droplets of epoxy resin (ER) in a liquid state. The photoisomerization of C6 induced by UV irradiation and heating alternatively precipitates out and dissolves COPV in ER and changes the photoluminescence color, while maintaining the optical microresonator properties. This study will open a promising way for assembling/disassembling novel emission color‐switchable systems.
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Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Photochromic and Fluorescence Chemistry · Porphyrin and Phthalocyanine Chemistry
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Affiliations
Department of Materials Science Faculty of Pure and Applied Sciences and Tsukuba Research Center for Energy Materials Science (TREMS) University of Tsukuba 1‐1‐1 Tennodai Tsukuba Ibaraki 305‐8573 Japan
Research Institute for Advanced Electronics and Photonics National Institute of Advanced Industrial Science and Technology (AIST) Central 5, 1‐1‐1 Higashi Tsukuba Ibaraki 305‐8565 Japan
School of Environment Science and Research Center for Molecular Design Kochi University of Technology 185 Miyanokuchi, Tosayamada Kami Kochi 782‐8502 Japan
References (45)
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