Peculiarities of exited state intramolecular proton transfer in 2-amino-3-(2′-benzazolyl)-quinolines
- Authors: Khimich M.N.1, Ivanov V.L.1, Mel’nikov M.Y.1, Uzhinov B.M.1
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Affiliations:
- Moscow State University
- Issue: Vol 51, No 1 (2017)
- Pages: 17-23
- Section: Photochemistry
- URL: https://journal-vniispk.ru/0018-1439/article/view/157094
- DOI: https://doi.org/10.1134/S0018143916060059
- ID: 157094
Cite item
Abstract
It has been shown that a low fluorescence quantum yield of 2-amino-3-(2′-benzoxazolyl)-quinoline (ABO) and 2-amino-3-(2′-benzothiazolyl)-quinoline (ABT) is due to the relaxation process caused by excited state intramolecular proton transfer (ESIPT). Quantum-chemical calculations have revealed that ESIPT in these compounds is characterized by overcoming a potential barrier, with the lower basicity of the proton-accepting moiety in ABO resulting in a higher barrier than in ABT and, thereby, determining a substantial difference in their fluorescence quantum yields.
About the authors
M. N. Khimich
Moscow State University
Author for correspondence.
Email: mikhail.nick.kh@gmail.com
Russian Federation, Moscow, 119991
V. L. Ivanov
Moscow State University
Email: mikhail.nick.kh@gmail.com
Russian Federation, Moscow, 119991
M. Ya. Mel’nikov
Moscow State University
Email: mikhail.nick.kh@gmail.com
Russian Federation, Moscow, 119991
B. M. Uzhinov
Moscow State University
Email: mikhail.nick.kh@gmail.com
Russian Federation, Moscow, 119991
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