Sciact
  • EN
  • RU

51V and 13C NMR Spectroscopic Study of the Peroxovanadium Intermediates in Vanadium Catalyzed Enantioselective Oxidation of Sulfides Научная публикация

Журнал Journal of Molecular Catalysis A: Chemical
ISSN: 1381-1169
Вых. Данные Год: 2001, Том: 171, Страницы: 73-80 Страниц : 8 DOI: 10.1016/S1381-1169(01)00106-6
Ключевые слова Asymmetric oxidations, Chiral Schiff bases, Intermediates, NMR, Peroxo complexes of vanadium, Sulfoxides
Авторы Bryliakov K.P. 1 , Karpy'shev N.N. 1 , Fominsky S.A. 1 , Tolstikov A.G. 1 , Talzi E.P. 1
Организации
1 Boreskov Institute of Catalysis, Pr. Ac. Lavrentieva 5, Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 00-03-32438

Реферат: Using 13C and 13C{1H} NMR spectroscopy, structure and reactivity of vanadium peroxo complexes formed in the catalytic system [VO(Oi-Pr)3]/Schiff base ligand/H2O2 for enantioselective oxidation of sulfides were concerned. It was shown, that two types of monoperoxo vanadium(V) species bearing one Schiff base ligand per vanadium atom predominated in this catalytic system at low temperature. These complexes are unstable at room temperature and decompose with half-life time of 20 min. The rate of this decomposition markedly increases in the presence of methyl phenyl sulfide. Addition of a fresh portion of H2O2 restores partially the peroxo vanadium intermediates. These data suggest that the peroxo vanadium species observed could be the active intermediates in enantioselective oxidation of sulfides. Two types of peroxo complexes found, probably, differ in the mode of Schiff base ligand coordination
Библиографическая ссылка: Bryliakov K.P. , Karpy'shev N.N. , Fominsky S.A. , Tolstikov A.G. , Talzi E.P.
51V and 13C NMR Spectroscopic Study of the Peroxovanadium Intermediates in Vanadium Catalyzed Enantioselective Oxidation of Sulfides
Journal of Molecular Catalysis A: Chemical. 2001. V.171. P.73-80. DOI: 10.1016/S1381-1169(01)00106-6 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 21 сент. 2000 г.
Принята к публикации: 10 янв. 2001 г.
Опубликована online: 31 мая 2001 г.
Опубликована в печати: 12 июн. 2001 г.
Идентификаторы БД:
Web of science: WOS:000169317100007
Scopus: 2-s2.0-0035849498
РИНЦ: 13374755
Chemical Abstracts: 2001:419458
Chemical Abstracts (print): 135:226591
OpenAlex: W1965740784
Цитирование в БД:
БД Цитирований
Web of science 50
Scopus 59
РИНЦ 59
OpenAlex 53
Альметрики: