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Catalyzed Transfer Hydrogenation by 2-propanol for Highly Selective PAHs Reduction Научная публикация

Журнал Catalysis Today
ISSN: 0920-5861 , E-ISSN: 1873-4308
Вых. Данные Год: 2021, Том: 379, Страницы: 15-22 Страниц : 8 DOI: 10.1016/j.cattod.2020.06.060
Ключевые слова Polyaromatic hydrocarbons; 2-Propanol; Raney® nickel; Transfer hydrogenation; Hydrogenative dearomatization
Авторы Philippov A.A. 1 , Chibiryaev A.M. 1 , Martyanov O.N. 1
Организации
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Academician Lavrentiev Avenue 5, 630090 Novosibirsk, Russia

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 18-29-06022
2 Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) 075-15-2019-1876

Реферат: Catalytic hydrogenation of mono-, di- and trinuclear aromatic compounds has been studied under hydrogen transfer conditions at 150 °C and 82 °C in 2-PrOH as a hydrogen donor and with Raney® nickel as a catalyst. In contrast to conjugated or condensed aromatic rings, isolated ones demonstrated low reactivity in transfer hydrogenation (TH) that can be used to increase the hydrogenation selectivity of the reaction. So, naphthalene and biphenyl are partially hydrogenated into tetralin and cyclohexylbenzene, respectively, with excellent conversion (≥ 96%) and selectivity (≥ 98%) for 5–6 h at 82 °C. Increasing the reaction temperature to 150 °C results expectedly in the hydrogenation of second aromatic ring, which occurs slowly enough. Only 8% of decaline and 42% of dicyclohexyl, correspondingly, were obtained after 5 h at 150 °C. At the same time, TH of trinuclear anthracene and phenanthrene at 150 °C resulted in the formation of deeper hydrogenated octahydro-anthracenes and -phenanthrenes, respectively.
Библиографическая ссылка: Philippov A.A. , Chibiryaev A.M. , Martyanov O.N.
Catalyzed Transfer Hydrogenation by 2-propanol for Highly Selective PAHs Reduction
Catalysis Today. 2021. V.379. P.15-22. DOI: 10.1016/j.cattod.2020.06.060 WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 30 окт. 2019 г.
Принята к публикации: 23 июн. 2020 г.
Опубликована online: 30 июн. 2020 г.
Опубликована в печати: 1 нояб. 2021 г.
Идентификаторы БД:
Web of science: WOS:000686897100003
Scopus: 2-s2.0-85087773275
РИНЦ: 45481357
Chemical Abstracts: 2020:1391050
OpenAlex: W3037248221
Цитирование в БД:
БД Цитирований
Scopus 18
РИНЦ 13
Web of science 17
OpenAlex 19
Альметрики: