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Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene Научная публикация

Журнал Molecules
, E-ISSN: 1420-3049
Вых. Данные Год: 2021, Том: 26, Номер: 3, Номер статьи : 526, Страниц : DOI: 10.3390/molecules26030526
Ключевые слова perfluorinated tetrathiacalix[4]arene; perfluoro-m-xylene; dioxadithiacalix[4]arenes; tetraoxadithiacalix[6]arene; thiourea; 2; 5-difluoro-4; 6-bis(trifluoromethyl)benzene-1; 3-dithiol; X-ray analyses
Авторы Kovtonyuk Vladimir N. 1 , Gatilov Yuri V. 1 , Nikul'shin Pavel V. 1 , Bredikhin Roman A. 1
Организации
1 (Данные Web of science) SB RAS, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Academician Lavrentjev Ave, Novosibirsk 630090, Russia

Реферат: Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 degrees C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively.
Библиографическая ссылка: Kovtonyuk V.N. , Gatilov Y.V. , Nikul'shin P.V. , Bredikhin R.A.
Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene
Molecules. 2021. V.26. N3. 526 . DOI: 10.3390/molecules26030526 WOS Scopus РИНЦ OpenAlex
Файлы: Полный текст от издателя
Даты:
Опубликована online: 20 янв. 2021 г.
Идентификаторы БД:
Web of science: WOS:000615460700001
Scopus: 2-s2.0-85100480243
РИНЦ: 46745294
OpenAlex: W3122502936
Цитирование в БД:
БД Цитирований
Web of science 3
Scopus 3
РИНЦ 1
OpenAlex 3
Альметрики: