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A novel method of alkoxyamines homolysis activation via photochemical rearrangement Научная публикация

Журнал Physical Chemistry Chemical Physics
ISSN: 1463-9076 , E-ISSN: 1463-9084
Вых. Данные Год: 2024, Том: 26, Номер: 12, Страницы: 9754-9762 Страниц : 9 DOI: 10.1039/d3cp05815h
Авторы Cherkasov Sergey 1 , Parkhomenko Dmitriy 2 , Morozov Denis 2 , Bagryanskaya Elena 2
Организации
1 Novosibirsk State University
2 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of Siberian Branch of Russian Academy of Sciences

Реферат: Abstract We proposed the nitrone-oxaziridine rearrangement as a novel method for photochemical activation for the homolysis of alkoxyamine in Nitroxide-Mediated Polymerization. The photoisomerization of aldo-/ketonitrone-group into oxaziridine one in 2,5-dihydroimidazole 3-oxide-based alkoxyamines was studied; the products of photolysis have been identified, and quantum yields were measured. Conversion of the nitrone group into oxaziridine one was found to decrease the activation energy of alkoxyamine homolysis by ca. 10 kJ/mol.
Библиографическая ссылка: Cherkasov S. , Parkhomenko D. , Morozov D. , Bagryanskaya E.
A novel method of alkoxyamines homolysis activation via photochemical rearrangement
Physical Chemistry Chemical Physics. 2024. V.26. N12. P.9754-9762. DOI: 10.1039/d3cp05815h WOS Scopus OpenAlex
Даты:
Поступила в редакцию: 29 нояб. 2023 г.
Принята к публикации: 28 февр. 2024 г.
Опубликована online: 4 мар. 2024 г.
Идентификаторы БД:
Web of science: WOS:001183502400001
Scopus: 2-s2.0-85187649261
OpenAlex: W4392403354
Цитирование в БД:
БД Цитирований
OpenAlex 1
Web of science 1
Scopus 1
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