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Chiral C-2-Symmetric Diimines with 4,5-Diazafluorene Units Научная публикация

Журнал Molecules
, E-ISSN: 1420-3049
Вых. Данные Год: 2019, Том: 24, Номер: 17, Номер статьи : 3186, Страниц : DOI: 10.3390/molecules24173186
Ключевые слова pinocarvone oxime; 4,5-diazafluorenon-9-one; chiral dipinodiazafluorenone; aromatic diamines; stable chiral diimines
Авторы Vasilyev Eugene S. 1 , Bizyaev Sergey N. 1 , Komarov Vladislav Yu. 2,3 , Gatilov Yury V. 1 , Tkachev Alexey V. 1,3
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Academician Lavrentiev Ave, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, Nikolaev Inst Inorgan Chem, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia

Реферат: A synthetic approach to a new group of stable chiral C-2-symmetric diimines with the 4,5-diazafluorene core has been developed based on condensation of dipinodiazafluorene with aromatic diamines. The chemical structures of new compounds were proven by spectroscopic methods and X-ray crystallography. All the compounds form solvates with organic solvents (chloroform, benzene, 1,4-dioxane) and water. Specific spectral data of the new compounds are explained using calculated data (DFT). Diimines of the pinodiazafluorene series give colored reactions with transition metal ions and can be regarded as prospective polydentate ligands with interesting luminescent and chiroptical properties.
Библиографическая ссылка: Vasilyev E.S. , Bizyaev S.N. , Komarov V.Y. , Gatilov Y.V. , Tkachev A.V.
Chiral C-2-Symmetric Diimines with 4,5-Diazafluorene Units
Molecules. 2019. V.24. N17. 3186 . DOI: 10.3390/molecules24173186 WOS Scopus РИНЦ OpenAlex
Файлы: Полный текст от издателя
Даты:
Опубликована online: 2 сент. 2019 г.
Идентификаторы БД:
Web of science: WOS:000488613700166
Scopus: 2-s2.0-85071736156
РИНЦ: 41636829
OpenAlex: W2971583560
Цитирование в БД:
БД Цитирований
Web of science 4
Scopus 4
РИНЦ 5
OpenAlex 7
Альметрики: