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Effect of photoswitchable azobenzene side chain on coumarins optical and chiroptical behavior
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YASEMİN AKDİŞ Master Thesis.pdf
Yasemin Akdiş.pdf
Date
2025-3-14
Author
Akdiş, Yasemin
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The conformation/configuration of the side chain in coumarin derivatives significantly impacts their features and applications, making them versatile in various scientific and industrial fields. This versatility can be attributed to their capacity to modify chemical reactivity, binding interactions, pharmacological activity, stability, solubility, and material qualities. In this context, the objective of this study was to investigate the effect of a change in the conformation/configuration of the azobenzene-containing side chain of coumarin linked to 3 rd and 7th positions. For this purpose, eight different compounds were synthesized. The fact that azobenzene derivatives can be irradiated with a specific wavelength of light to achieve photoisomerization from the trans to the cis form has allowed it to be used as a convenient and controllable side chain. To investigate the optical and chiroptical properties of the synthesized materials, we conducted a series of UV-Vis, fluorescence, and circular dichroism studies in various solvents, complemented by theoretical studies.
Subject Keywords
Azobenzene
,
Coumarin
,
Chirality
,
Photoisomerization
URI
https://hdl.handle.net/11511/114193
Collections
Graduate School of Natural and Applied Sciences, Thesis
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Y. Akdiş, “Effect of photoswitchable azobenzene side chain on coumarins optical and chiroptical behavior,” M.S. - Master of Science, Middle East Technical University, 2025.