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Mechanism of replacement of the nitro group and fluorine atom in meta-substituted nitrobenzenes by phenols in the presence of potassium carbonate Научная публикация

Журнал Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Вых. Данные Год: 2005, Том: 41, Номер: 7, Страницы: 978-983 Страниц : 6 DOI: 10.1007/s11178-005-0280-1
Авторы Khalfina IA 1 , Vlasov VM 1
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: The relative mobilities of the nitro group and fluorine atom in 1,3-dinitrobenzene and 1-fluoro3-nitrobenzene by the action of phenols in the presence of potassium carbonate in dimethylformamide at 95-125 degrees C were studied by the competing reaction method. The rate constant ratios k(NO2)/k(F) were correlated with the differences between the corresponding activation parameters (Delta Delta H-double dagger and Delta AS(double dagger)). The greater mobility of the nitro group was found to be determined by the entropy control of the reactivity of arenes. The activation parameters (Delta H-double dagger and Delta S-double dagger) were calculated, and the enthalpy entropy compensation effect was revealed. The reaction mechanism is discussed.
Библиографическая ссылка: Khalfina I. , Vlasov V.
Mechanism of replacement of the nitro group and fluorine atom in meta-substituted nitrobenzenes by phenols in the presence of potassium carbonate
Russian Journal of Organic Chemistry. 2005. V.41. N7. P.978-983. DOI: 10.1007/s11178-005-0280-1 WOS Scopus РИНЦ OpenAlex
Оригинальная: Халфина И.А. , Власов В.М.
О механизме unco-замещения нитро-группы и атома фтора в мета-прот-водных нитробензола под действием фенолов в присутствии карбоната калия
Журнал органической химии (RUSS J ORG CHEM+). 2005. Т.41. №7. С.999-1005. РИНЦ
Даты:
Опубликована в печати: 1 июл. 2005 г.
Идентификаторы БД:
Web of science: WOS:000232449000007
Scopus: 2-s2.0-25144452868
РИНЦ: 13486297
OpenAlex: W1979054548
Цитирование в БД:
БД Цитирований
Web of science 8
Scopus 10
РИНЦ 10
OpenAlex 8
Альметрики: