Tautomerism of anthraquinones: IV. 1-Hydroxy-9,10-anthraquinone and its substituted derivatives

1-Hydroxyanthraquinone and its substituted derivatives exist as equilibrium mixtures of four tautomers and rotational isomers. Their anions have 9,10-and 1,10-quinoid structures. Each tautomer or conformer is characterized by a single π1,π*band in the electronic absorption spectrum. © 2006 Nauka/Interperiodica.

Авторы
Номер выпуска
10
Язык
Английский
Страницы
1469-1472
Статус
Опубликовано
Том
42
Год
2006
Организации
  • 1 Russian University of Peoples' Friendship, P.O. Box 453, Moscow 127349, Russian Federation
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/3331/