Tautomerism of anthraquinones: III. Tautomerization and rotational isomerization as processes responsible for the appearance of several π1,π*-bands in the absorption spectra of hydroxy-substituted quinones

Hydroxy-substituted anthraquinones, naphthoquinones, and naphthacenequinones exist as equilibrium mixtures of different tautomers and rotational isomers which give rise to several π1,π*bands in their electronic absorption spectra. Each π1,π*band can be assigned to a particular tautomer and conformer on the basis of the substituent constants σA. © 2006 Nauka/Interperiodica.

Авторы
Номер выпуска
10
Язык
Английский
Страницы
1464-1468
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/3328/