Partial deuterium substitution as a tool for identification of the most stable conformer of a polyatomic molecule. A case of the 2,5-bis(2-benzoxazolyl)-1,4-dimethoxybenzene in supersonic jet-Reference-Cited by-同舟云学术

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Partial deuterium substitution as a tool for identification of the most stable conformer of a polyatomic molecule. A case of the 2,5-bis(2-benzoxazolyl)-1,4-dimethoxybenzene in supersonic jet

Published:2012-12 Issue: Volume:554 Page:43-46
ISSN:0009-2614
Container-title:Chemical Physics Letters
language:en
Short-container-title:Chemical Physics Letters

Author:

Sepioł J.,Grabowska A.,Kijak M.,Borowicz P.,Mengesha E.,Nowacki J.

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Reference20 articles.

1. Intramolecular single and double proton transfer in benzoxazole derivatives

2. Dual fluorescence and excited-state intramolecular proton transfer in jet-cooled 2,5-bis(2-benzoxazolyl)hydroquinone

3. Kinetics of excited-state proton transfer in double benzoxazoles: 2,5-bis(2-benzoxazolyl)-4-methoxyphenol

4. Fluorescence studies of excited state intramolecular proton transfer (ESIPT) in molecules isolated in solid argon: 3-hydroxyflavone and 2,5-bis(2-benzoxazolyl)hydroquinone

5. Picosecond kinetics of the excited-state intramolecular proton transfer reaction: Confirmation of the intrinsic potential barrier in 2,5-bis-(benzoxazolyl)-hydroquinone

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1. Reactivity and H–D Exchange Rate of the α-Methylene of Deoxyvasicinone and its Homologs;Chemistry of Natural Compounds;2014-11-27

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