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Some Like It Weak: Different Activity of Raney® Nickel in Transfer Hydrogenation under Air and Inert Atmosphere Научная публикация

Журнал Applied Catalysis A: General
ISSN: 0926-860X , E-ISSN: 1873-3875
Вых. Данные Год: 2020, Том: 605, Номер статьи : 117788, Страниц : 11 DOI: 10.1016/j.apcata.2020.117788
Ключевые слова Transfer hydrogenolysis; catalytic hydrogenation; carbonyl compounds; Ni catalyst; H-transfer; reduction; surface; 2-propanol; deoxygenation; activation
Авторы Philippov A.A. 1 , Chibiryaev A.M. 1 , Prosvirin I.P. 1 , Martyanov O.N. 1
Организации
1 Boreskov Institute of Catalysis SB RAS, Academician Lavrentiev ave. 5, Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 18-29-06022

Реферат: Transfer hydrogenation (TH) of six substrates catalyzed by Raney® nickel and conducted at 150 °C for 5 h under air or argon was studied. Significant decrease of conversion was observed under air as compared with TH under argon: 57% vs. 98% for menthone and 39% vs. 54% for camphor, respectively. Regardless of different reaction atmosphere used, aluminum segregated on the catalyst surface to form micron-sized alumina crystallites to modify the adsorption capacity, to inhibit the catalyst activity and to change the products selectivity of TH. Moreover, the changes of the catalyst structure under air entailed the change of reaction rates of both hydrodeoxygenation and dearomatization of acylbenzenes (ketones), as well as benzylic alcohols. Thus, manipulating by reaction atmosphere of TH catalyzed by Raney® nickel can be considered as an efficient tool to govern a chemo-, regio- and stereo-selectivity of products.
Библиографическая ссылка: Philippov A.A. , Chibiryaev A.M. , Prosvirin I.P. , Martyanov O.N.
Some Like It Weak: Different Activity of Raney® Nickel in Transfer Hydrogenation under Air and Inert Atmosphere
Applied Catalysis A: General. 2020. V.605. 117788 :1-11. DOI: 10.1016/j.apcata.2020.117788 WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 9 апр. 2020 г.
Принята к публикации: 13 авг. 2020 г.
Опубликована online: 14 авг. 2020 г.
Опубликована в печати: 5 сент. 2020 г.
Идентификаторы БД:
Web of science: WOS:000576786900008
Scopus: 2-s2.0-85089811368
РИНЦ: 45340392
Chemical Abstracts: 2020:1705912
OpenAlex: W3049066833
Цитирование в БД:
БД Цитирований
Scopus 7
Web of science 7
РИНЦ 6
OpenAlex 7
Альметрики: