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Chemically Triggered C–ON Bond Homolysis in Alkoxyamines. Part 2: DFT Investigation and Application of the pH Effect on NMP Научная публикация

Журнал Macromolecular Rapid Communications
Вых. Данные Год: 2012, Том: 33, Номер: 2, Страницы: 152-157 Страниц : 6 DOI: 10.1002/marc.201100590
Ключевые слова C—ON bond homolysis, kinetics, nitroxide-mediated polymerization, pH effect polymerization
Авторы Bagryanskaya Elena 1 , Brémond Paul 2 , Edeleva Mariya 1 , Marque Sylvain R.A. 2 , Parkhomenko Dmitriy 1 , Roubaud Valérie 2 , Siri Didier 2
Организации
1 International Tomography Center SB RAS
2 Aix Marseille Univ, CNRS, ICR

Реферат: In recent work, a 15-fold increase in the C–ON bond homolysis rate constant kd of 4-pyridylethyl-SG1-based alkoxyamine was observed upon protonation of the pyridyl moiety in organic solvent. In this report, the pH dependence of kd (pKa = 4.7) is investigated in D2O/CD3OD (v/v 1:1). A 64-fold increase in kd is observed at acidic pH. Calculations show that the increase in kd upon protonation is due to both an increase in the stabilization of the protonated 4-pyridylethyl radical and an increase of the destabilization of the starting materials through an increase in the polarity of the alkyl fragment. This new alkoxyamine is applied to NMP of styrene and sodium styrene sulfonate.
Библиографическая ссылка: Bagryanskaya E. , Brémond P. , Edeleva M. , Marque S.R.A. , Parkhomenko D. , Roubaud V. , Siri D.
Chemically Triggered C–ON Bond Homolysis in Alkoxyamines. Part 2: DFT Investigation and Application of the pH Effect on NMP
Macromolecular Rapid Communications. 2012. V.33. N2. P.152-157. DOI: 10.1002/marc.201100590 WOS Scopus РИНЦ OpenAlex
Даты:
Поступила в редакцию: 7 сент. 2011 г.
Опубликована online: 21 нояб. 2011 г.
Идентификаторы БД:
Web of science: WOS:000299102700008
Scopus: 2-s2.0-84856022363
РИНЦ: 17974221
OpenAlex: W2100788317
Цитирование в БД:
БД Цитирований
OpenAlex 34
Web of science 33
Scopus 33
Альметрики: