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Clean Catalytic Oxidation of 8-Hydroxyquinoline to Quinoline-5,8-dione with tBuOOH in the Presence of Covalently Bound FePcS-SiO2 Catalysts Научная публикация

Журнал Green Chemistry
ISSN: 1463-9262 , E-ISSN: 1463-9270
Вых. Данные Год: 2010, Том: 12, Номер: 6, Страницы: 1076-1082 Страниц : 7 DOI: 10.1039/b923674k
Ключевые слова ANTITUMOR ANTIBIOTIC STREPTONIGRIN; SELECTIVE OXIDATION; HETEROCYCLIC QUINONES; BIOLOGICAL EVALUATION; AROMATIC-COMPOUNDS; AGENTS; DERIVATIVES; PHENOLS; ANALOGS; INHIBITORS
Авторы Zalomaeva Olga V. 1 , Sorokin Alexander B. 2 , Kholdeeva Oxana A. 1
Организации
1 Boreskov Institute of Catalysis
2 Institut de Recherches sur la Catalyse

Информация о финансировании (4)

1 Российский фонд фундаментальных исследований 05-03-34760
2 Российский фонд фундаментальных исследований 09-03-93109
3 French National Centre for Scientific Research
4 The French National Research Agency ANR-08-BLAN-0183-01

Реферат: The clean catalytic oxidation of 8-hydroxyquinoline (8-HQ) with tert-butyl hydroperoxide to quinoline-5,8-dione (QD), a molecular framework fragment of antitumor compounds, over silica-supported iron tetrasulfophthalocyanine catalysts (FePcS) is reported. The pronounced influence of the FePcS state (monomer vs. dimer) and the support (amorphous SiO2vs. mesoporous MCM-41) on the catalytic activity and selectivity is revealed. Depending on the catalyst structure, turnover frequency values determined from the initial rates of 8-HQ consumption varied from 215 to 3570 h−1.The effects of solvent, temperature, reagent concentrations and catalyst amounts on the substrate conversion and QD selectivity were studied to optimize the reaction conditions. With an optimal catalyst, the yield of the target product reached 66%. The truly heterogeneous nature of the catalysis was also demonstrated.
Библиографическая ссылка: Zalomaeva O.V. , Sorokin A.B. , Kholdeeva O.A.
Clean Catalytic Oxidation of 8-Hydroxyquinoline to Quinoline-5,8-dione with tBuOOH in the Presence of Covalently Bound FePcS-SiO2 Catalysts
Green Chemistry. 2010. V.12. N6. P.1076-1082. DOI: 10.1039/b923674k WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 13 нояб. 2009 г.
Принята к публикации: 15 мар. 2010 г.
Опубликована online: 22 апр. 2010 г.
Опубликована в печати: 8 июн. 2010 г.
Идентификаторы БД:
Web of science: WOS:000278534900024
Scopus: 2-s2.0-77953318938
РИНЦ: 15317866
Chemical Abstracts: 2010:708185
Chemical Abstracts (print): 153:505262
OpenAlex: W2042702581
Цитирование в БД:
БД Цитирований
Web of science 13
Scopus 15
РИНЦ 15
OpenAlex 14
Альметрики: