Molecular design and synthesis of methoxy-substitued spiropyrans with photomodulated NIR-fluorescence
Author:
Funder
Russian Science Foundation
State task of the Ministry of Science and Higher Education of Russia
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s43630-023-00479-1.pdf
Reference89 articles.
1. Bouas-Laurent, H., & Dürr, H. (2001). Organic photochromism (IUPAC Technical Report). Pure and Applied Chemistry, 73, 639–665. https://doi.org/10.1351/pac200173040639
2. Lukyanov, B. S., & Lukyanova, M. B. (2005). Spiropyrans: Synthesis, properties, and application. (Review). Chemistry of Heterocyclic Compounds, 4, 281–311. https://doi.org/10.1007/s10593-005-0148-x
3. Pugachev, A. D., Mukhanov, E. L., Ozhogin, I. V., Kozlenko, A. S., Metelitsa, A. V., & Lukyanov, B. S. (2021). Isomerization and changes of the properties of spiropyrans by mechanical stress: Advances and outlook. Chemistry of Heterocyclic Compounds, 57, 122–130. https://doi.org/10.1007/s10593-021-02881-y
4. Rad, J. K., Balzade, Z., & Mahdavian, A. R. (2022). Spiropyran-based advanced photoswitchable materials: A fascinating pathway to the future stimuli-responsive devices. Journal of Photochemistry and Photobiology C: Photochemistry Reviews, 51, 100487. https://doi.org/10.1016/j.jphotochemrev.2022.100487
5. Kozlenko, A. S., Ozhogin, I. V., Pugachev, A. D., Lukyanova, M. B., El-Sewify, I. M., & Lukyanov, B. S. (2023). A modern look at spiropyrans: From single molecules to smart materials. Topics in Current Chemistry, 381, 8. https://doi.org/10.1007/s41061-022-00417-2
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