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Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine Научная публикация

Журнал Organic and Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2021, Том: 19, Номер: 4, Страницы: 866-872 Страниц : 7 DOI: 10.1039/d0ob01893g
Авторы Genaev Alexander M. 1 , Salnikov George E. 1 , Koltunov Konstantin Yu. 2,3
Организации
1 (Данные Web of science) Vorozhtsov Novosibirsk Inst Organ Chem, Pr Lavrentieva 9, Novosibirsk 630090, Russia
2 (Данные Web of science) Boreskov Inst Catalysis, Pr Lavrentieva 5, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Univ, Pirogova 2, Novosibirsk 630090, Russia

Реферат: Stimuli-responsive and, in particular, temperature-responsive smart materials have recently gained much attention in a variety of applications. On the other hand, 4-(dimethylamino)pyridine (DMAP) and related structures are widely used as nucleophilic catalysts and also as specific parts of rationally designed molecules, where reversible reactions of the pyridinic nitrogen with electrophiles are involved. In our study, we have found an unexpectedly significant impact of temperature on the protonation degree of DMAP derivatives, especially in the case of protonation of the 4-(dimethylamino)-1-(2,3,5,6-tetrafluoropyridin-4-yl)pyridinium cation, derived from the reaction of DMAP with pentafluoropyridine. Thus, when dissolved in the TfOH-SO2ClF-CD2Cl2 acid system at 30 degrees C, this cation underwent a slight (<7%) protonation on the dimethylamino group, while the temperature decrease to -70 degrees C resulted in its complete protonation. Notably, such a scale of this phenomenon has never been observed before for other weak nucleophiles, being many times lower at the same change of temperature. The mechanistic aspects of these intriguing results are discussed.
Библиографическая ссылка: Genaev A.M. , Salnikov G.E. , Koltunov K.Y.
Unusual temperature-sensitive protonation behaviour of 4-(dimethylamino)pyridine
Organic and Biomolecular Chemistry. 2021. V.19. N4. P.866-872. DOI: 10.1039/d0ob01893g WOS Scopus РИНЦ OpenAlex
Идентификаторы БД:
Web of science: WOS:000614577400017
Scopus: 2-s2.0-85100392285
РИНЦ: 44957999
OpenAlex: W3111586764
Цитирование в БД:
БД Цитирований
Web of science 6
Scopus 4
РИНЦ 4
OpenAlex 6
Альметрики: