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1,1-Difluoronaphthalen-2(1H)-ones as building blocks for fluorinated tetraphenes Научная публикация

Журнал Journal of Fluorine Chemistry
ISSN: 0022-1139
Вых. Данные Год: 2018, Том: 210, Страницы: 88-93 Страниц : 6 DOI: 10.1016/j.jfluchem.2018.03.008
Ключевые слова Diels-Alder cycloaddition; Organofluorine compounds; Polycyclic aromatic hydrocarbons
Авторы Dyan Ok Ton 1 , Zaikin Pavel A. 1 , Fadeev Dmitry S. 1 , Gatilov Yuri V. 1,2 , Borodkin Gennady I. 1,2
Организации
1 (Данные Web of science) NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Acad Lavrentiev Ave, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, 2 Pirogov St, Novosibirsk 630090, Russia

Реферат: 1,1-Difluoronaphthalen-2(1H)-ones were used as building blocks for synthesis of functionalized fluorinated tetraphenones via Diels-Alder reaction. Two effective methods of tetraphenone reductive aromatization were proposed. Fully aromatic stable fluorinated tetraphene derivative with high solubility and HOMO-LUMO gap of 3.08 eV was obtained.
Библиографическая ссылка: Dyan O.T. , Zaikin P.A. , Fadeev D.S. , Gatilov Y.V. , Borodkin G.I.
1,1-Difluoronaphthalen-2(1H)-ones as building blocks for fluorinated tetraphenes
Journal of Fluorine Chemistry. 2018. V.210. P.88-93. DOI: 10.1016/j.jfluchem.2018.03.008 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июн. 2018 г.
Идентификаторы БД:
Web of science: WOS:000433266600009
Scopus: 2-s2.0-85044106907
РИНЦ: 35495900
OpenAlex: W2794356578
Цитирование в БД:
БД Цитирований
Web of science 7
Scopus 7
РИНЦ 6
OpenAlex 6
Альметрики: