Sciact
  • EN
  • RU

Catalytic Performance of Zr‐Based Metal‐Organic Frameworks Zr‐abtc and MIP‐200 in Selective Oxidations with H2O2 Научная публикация

Журнал Chemistry - A European Journal
ISSN: 0947-6539 , E-ISSN: 1521-3765
Вых. Данные Год: 2021, Том: 27, Номер: 23, Страницы: 6985-6992 Страниц : 8 DOI: 10.1002/chem.202005152
Ключевые слова Metal-organic frameworks, Hydrogen peroxide, Epoxidation, Zr, α,β-Unsaturated Ketones
Авторы Maksimchuk Nataliya V. 1 , Ivanchikova Irina D. 1 , Cho Kyung Ho 2 , Zalomaeva Olga V. 1 , Evtushok Vasiliy Yu. 1,3 , Larionov Kirill P. 1,3 , Glazneva Tatiana S. 1 , Chang Jong-San 2,4 , Kholdeeva Oxana A. 1
Организации
1 Boreskov Institute of Catalysis
2 Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology
3 Department of Natural Sciences, Novosibirsk State University
4 Department of Chemistry, Sungkyunkwan University

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 18-29-04022
2 Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) 0239-2021-0009

Реферат: Catalytic performance of Zr-abtc and MIP-200 metal-organic frameworks consisted of 8-connected Zr6-clusters and tetratopic linkers was investigated in H2O2-based selective oxidations and compared with that of 12-coordinated UiO-66 and UiO-67. Zr-abtc demonstrated advantages in both substrate conversion and product selectivity for epoxidation of electron-deficient C=C bonds in α,β-unsaturated ketones. A significant predomination of 1,2-epoxide in carvone epoxidation, coupled to high sulfone selectivity in thioether oxidation, points to a nucleophilic oxidation mechanism over Zr-abtc. The superior catalytic performance in the epoxidation of unsaturated ketones correlates with a larger amount of weak basic sites in Zr-abtc. Electrophilic activation of H2O2 can also be realized, as evidenced by high activity of Zr-abtc in epoxidation of electron-rich C=C bond in caryophyllene. XRD and FTIR studies confirmed the retention of the Zr-abtc structure after the catalysis. Low activity of MIP-200 in H2O2-based oxidations is most likely related to its specific hydrophilicity, which disfavors adsorption of organic substrates and H2O2.
Библиографическая ссылка: Maksimchuk N.V. , Ivanchikova I.D. , Cho K.H. , Zalomaeva O.V. , Evtushok V.Y. , Larionov K.P. , Glazneva T.S. , Chang J-S. , Kholdeeva O.A.
Catalytic Performance of Zr‐Based Metal‐Organic Frameworks Zr‐abtc and MIP‐200 in Selective Oxidations with H2O2
Chemistry - A European Journal. 2021. V.27. N23. P.6985-6992. DOI: 10.1002/chem.202005152 WOS Scopus РИНЦ CAPlus PMID OpenAlex
Даты:
Поступила в редакцию: 1 дек. 2020 г.
Принята к публикации: 8 февр. 2021 г.
Опубликована online: 8 февр. 2021 г.
Опубликована в печати: 22 апр. 2021 г.
Идентификаторы БД:
Web of science: WOS:000628882000001
Scopus: 2-s2.0-85100933240
РИНЦ: 46748133
Chemical Abstracts: 2021:645633
PMID (PubMed): 33559238
OpenAlex: W3126712626
Цитирование в БД:
БД Цитирований
Scopus 22
Web of science 21
РИНЦ 19
OpenAlex 24
Альметрики: