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Assembling triazolated calix[4]semitubes by means of copper(I)-catalyzed azide–alkyne cycloadditionстатья Исследовательская статья
Статья опубликована в высокорейтинговом журнале
Информация о цитировании статьи получена из
Web of Science,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 17 августа 2021 г.
- Авторы: Gorbunov Alexander, Ozerov Nikolay, Malakhova Maria, Eshtukov Artur, Cheshkov Dmitry, Bezzubov Stanislav, Kovalev Vladimir, Vatsouro Ivan
- Журнал: Organic Chemistry Frontiers
- Том: 8
- Номер: 14
- Год издания: 2021
- Первая страница: 3853
- Последняя страница: 3866
- DOI: 10.1039/D1QO00636C
- Аннотация: Nine pairs of cone and 1,3-alternate calix[4]arenes having distal propargyl or 2-azidoethyl groups at their phenolic oxygen atoms were thoroughly studied during macrocyclization under copper(I) catalysis (CuAAC, copper(I)-catalyzed azide–alkyne cycloaddition). Though the formation of undesired polymeric species was not avoidable, the conditions for the preparation and purification of calix[4]semitubes comprising two calixarenes linked by two triazole units were found for all the bis(alkyne)/bis(azide) combinations, and the features of the reacting counterparts which affected the semitube/polymer ratio were analyzed. Formation of larger multi(macrocycles) was also observed in the interactions of sterically hindered bis(alkyne)/bis(azide) pairs under CuAAC conditions that was confirmed by mass spectrometry and diffusion NMR measurements. The molecular structures of the prepared triazolated multi(macrocycles) were confirmed using X-ray diffraction data in most cases. A preliminary complexation study demonstrated the ability of the triazolated calix[4]semitubes to bind Zn2+ or Ag+ cations, which was managed by the shape of the calixarene core (cone or 1,3-alternate) at the ‘alkyne sides’ of the semitubes and the steric hindrance in the molecules of the bis(calixarenes).
- Добавил в систему: Вацуро Иван Михайлович