Alkene Oxidation Catalyzed by Transition Metal Substituted Keggin-Type Heteropolyanions Научная публикация
Конференция |
EuropaCat-II: 2nd European Congress on Catalysis 03-08 сент. 1995 , Maastricht |
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Журнал |
Topics in Catalysis
ISSN: 1022-5528 , E-ISSN: 1572-9028 |
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Вых. Данные | Год: 1996, Том: 3, Номер: 3-4, Страницы: 313-325 Страниц : 13 DOI: 10.1007/BF02113857 | ||
Ключевые слова | Alkene oxidation, Dioxygen, Epoxidation mechanisms, Iodosylbenzene, Isobutyraldehyde, Oxidant activation, Tert-butyl hydroperoxide, Transition metal substituted heteropolytungstates | ||
Авторы |
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Организации |
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Информация о финансировании (1)
1 | International Science Foundation | RAUO00 |
Реферат:
Alkene oxidations with various oxidants (tert-butyl hydroperoxide, iodosylbenzene and molecular oxygen in the presence ofisobutyraldehyde (IBA)) catalyzed by transition metal monosubstituted heteropolyanions, PWHMO~ (PWn M; M = Co n, Mn n, Cu n, Ti N, Ru Iv, V v and NbV), have been studied. Orders of catalytic activity of PWHM are different for the oxidants studied. Radical chain mechanisms are proposed for t-BuOOH and O2/IBA. Preliminary coordination oftbe oxidant to PWHM is not a necessary step of its hemolytic activation. Epoxidation with PhIO requires its coordination to the catalyst and most likely includes the formation of active metal-oxo species.
Библиографическая ссылка:
Kholdeeva O.A.
, Grigoriev V.A.
, Maksimov G.M.
, Zamaraev K.I.
Alkene Oxidation Catalyzed by Transition Metal Substituted Keggin-Type Heteropolyanions
Topics in Catalysis. 1996. V.3. N3-4. P.313-325. DOI: 10.1007/BF02113857 WOS Scopus РИНЦ
Alkene Oxidation Catalyzed by Transition Metal Substituted Keggin-Type Heteropolyanions
Topics in Catalysis. 1996. V.3. N3-4. P.313-325. DOI: 10.1007/BF02113857 WOS Scopus РИНЦ
Даты:
Опубликована в печати: | 1 авг. 1996 г. |
Идентификаторы БД:
Web of science | WOS:A1996VG06600006 |
Scopus | 2-s2.0-0005575881 |
РИНЦ | 13224102 |
Chemical Abstracts | 1996:596529 |
Chemical Abstracts (print) | 125:275219 |
OpenAlex | W2085094613 |