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

Alexander M. Genaev, George E. Salnikov, Konstantin Yu Koltunov

Результат исследования: Научные публикации в периодических изданияхстатьярецензирование

Аннотация

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-CD2Cl2acid system at 30 °C, this cation underwent a slight (<7%) protonation on the dimethylamino group, while the temperature decrease to −70 °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.

Язык оригиналаанглийский
Страницы (с-по)866-872
Число страниц7
ЖурналOrganic and Biomolecular Chemistry
Том19
Номер выпуска4
DOI
СостояниеОпубликовано - 28 янв 2021

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