The Active Intermediates of Non-Heme-Iron-Based Systems for Catalytic Alkene Epoxidation with H2O2/CH3COOH Научная публикация
Журнал |
European Journal of Inorganic Chemistry
ISSN: 1434-1948 , E-ISSN: 1099-0682 |
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Вых. Данные | Год: 2007, Номер: 6, Страницы: 852-857 Страниц : 6 DOI: 10.1002/ejic.200600895 | ||
Ключевые слова | Acylperoxido complexes, EPR spectroscopy, Intermediates, NMR spectroscopy, Oxidation, Oxidoiron(IV) complexes, Paramagnetic | ||
Авторы |
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Организации |
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Информация о финансировании (1)
1 | Российский фонд фундаментальных исследований | 06-03-32214 |
Реферат:
Iron complexes with aminopyridine ligands [FeII(BPMEN)(CH3CN)2](ClO4)2 (1) [BPMEN = N,N′-dimethyl-N,N′-bis(2-pyridylmethyl)-1,2-diaminoethane] and [FeII(TPA)(CH3CN)2](ClO4)2 (2) [TPA = tris(2-pyridylmethyl)amine] are rare examples of iron-based catalysts for selective olefin epoxidation with H2O2/CH3COOH combination. Using 1,2H NMR and EPR spectroscopy, it was shown that the active species of the catalytic systems 1/H2O2/CH3COOH and 2/H2O2/CH3COOH are mononuclear iron(IV)-oxido complexes [(BPMEN)FeIV=O(S)]2+ and [(TPA)FeIV=O(S)]2+, respectively (S = solvent molecule). These intermediates are formed via decomposition of the corresponding acylperoxido complexes [(L)FeIII(O3CCH3)]2+ (L = BPMEN or TPA). The acylperoxido complex [(BPMEN)FeIII(O3CCD3)]2+ was identified in the catalytic system 1/H2O2/CD3COOD by 2H NMR spectroscopy. The improved epoxidation activity and selectivity of the catalytic systems 1/H2O2/CH3COOH and 2/H2O2/CH3COOH, with respect to 1/H2O2 and 2/H2O2, is caused by the effective formation of intermediates [(L)FeIV=O(S)]2+ via decomposition of the acylperoxido complexes [(L)FeIII(O3CCH3)]2+.
Библиографическая ссылка:
Duban E.A.
, Bryliakov K.P.
, Talsi E.P.
The Active Intermediates of Non-Heme-Iron-Based Systems for Catalytic Alkene Epoxidation with H2O2/CH3COOH
European Journal of Inorganic Chemistry. 2007. N6. P.852-857. DOI: 10.1002/ejic.200600895 WOS Scopus РИНЦ CAPlusCA OpenAlex
The Active Intermediates of Non-Heme-Iron-Based Systems for Catalytic Alkene Epoxidation with H2O2/CH3COOH
European Journal of Inorganic Chemistry. 2007. N6. P.852-857. DOI: 10.1002/ejic.200600895 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: | 25 сент. 2006 г. |
Опубликована online: | 15 янв. 2007 г. |
Опубликована в печати: | 1 февр. 2007 г. |
Идентификаторы БД:
Web of science: | WOS:000244906200008 |
Scopus: | 2-s2.0-34250710008 |
РИНЦ: | 13564075 |
Chemical Abstracts: | 2007:325235 |
Chemical Abstracts (print): | 148:144333 |
OpenAlex: | W2040924564 |