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Nucleophilic reactivity. Kinetics of reactions between diarylamines N-anions and hexafluorobenzene or pentafluoropyridine in dimethyl sulfoxide Научная публикация

Журнал Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Вых. Данные Год: 2001, Том: 37, Номер: 2, Страницы: 260-269 Страниц : 10 DOI: 10.1023/A:1012391231937
Авторы Os'kina I.A. 1 , Vlasov V.M. 1
Организации
1 (Данные Web of science) Russian Acad Sci, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: Rate constants of reactions between sodium salts of diarylamines N-anions and hexafluorobenzene and pentafluoropyridine in DMSO at 25 degreesC were determined. The Bronsted factors for substrates under consideration are 0.14 and 0.34 respectively. These data evidence a considerable effect of substrate electrophilicity on the reactivity of diarylamines N-anions in the SNAr reactions. Deviations of the Bronsted plot from linearity for the reactions of hexafluorobenzene with aryl-and diarylamines N-anions may be due to the difference in internal barriers of these reactions.
Библиографическая ссылка: Os'kina I.A. , Vlasov V.M.
Nucleophilic reactivity. Kinetics of reactions between diarylamines N-anions and hexafluorobenzene or pentafluoropyridine in dimethyl sulfoxide
Russian Journal of Organic Chemistry. 2001. V.37. N2. P.260-269. DOI: 10.1023/A:1012391231937 WOS Scopus РИНЦ РИНЦ OpenAlex
Идентификаторы БД:
Web of science: WOS:000170448400016
Scopus: 2-s2.0-0035255831
РИНЦ: 13372510 | 5048806
OpenAlex: W1229721811
Цитирование в БД:
БД Цитирований
Web of science 5
Scopus 4
РИНЦ 4
OpenAlex 4
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