Protonation of 1,4,5-tri-and 1,4,5,8-tetrahydroxyanthraquinones in sulfuric acid: Multistep reaction involving tautomers and conformers

The fi ne structure of the π l,π*-absorption of hydroxyanthraquinones solutions in sulfuric acid arises due to the existence of the protonated forms as equilibrium mixtures of tautomers and conformers distinguished by the positions of the π-bonds, charges, and the number of intramolecular hydrogen bonds. Using quantum-chemical calculations and correlation analysis of the absorption spectra tautomers were identifi ed of mono- and dications of 1,4,5-trihydroxyanthraquinone of 9,10-, 1,4-, and 1,10-isomeric structure. For 1,4,5,8-tetrahydroxyanthraquinone 9,10-, 1,4-, 1,10-, and 1,5-isomeric mono- and dications and their conformers were found. © 2012 Pleiades Publishing, Ltd.

Авторы
Номер выпуска
5
Язык
Английский
Страницы
667-675
Статус
Опубликовано
Том
48
Год
2012
Организации
  • 1 Russian University of Peoples' Friendship, Moscow, 117198, Russian Federation
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/2318/
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