|
ИСТИНА |
Войти в систему Регистрация |
ИСТИНА ЦЭМИ РАН |
||
Interaction of N,N'-Di(4-chlorophenyl)diimide 1,1'-Binaphtyl-4,4',5,5',8,8'-hexacarboxylic Acid with Thiourea Dioxide in Solution and Thin Filmстатья
Информация о цитировании статьи получена из
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 9 октября 2024 г.
- Авторы: Nikitin K.S., Polenov Yu V., Kazak A.V., Egorova E.V., Usol’tseva N.V.
- Журнал: Crystallography Reports
- Том: 65
- Номер: 5
- Год издания: 2020
- Издательство: Maik Nauka/Interperiodica Publishing
- Местоположение издательства: Russian Federation
- Первая страница: 779
- Последняя страница: 785
- DOI: 10.1134/s1063774520050156
- Аннотация: The reactions of interaction of N,N'-di(4-chlorophenyl)diimide 1,1'-binaphtyl-4,4',5,5',8,8'-hexa-carboxylic acid (cubogen red) with thiourea dioxide in a water-alkaline solution and a Langmuir–Blodgett thin film, obtained on quartz and silicon substrates, have been investigated. Electron absorption spectroscopy have revealed that the reaction of reductive cyclization of cubogen with formation of perylenetetracarboxylic acid diimide derivatives occurs in a water-alkaline solution. At the same time, the interaction of thiourea dioxide with a cubogen thin film does not lead to the formation of cyclization products; nevertheless, it changes the film structure. One might suggest that soluble leuco forms of J aggregates are formed in this case, whereas H aggregates remain intact in the structure.
- Добавил в систему: Никитин Константин Сергеевич