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Distinct Activity of the Oxyl Fe(III) -O Group in the Methane Dissociation by Activated Iron Hydroxide: DFT Predictions Научная публикация

Журнал Chemical Physics Letters
ISSN: 0009-2614 , E-ISSN: 1873-4448
Вых. Данные Год: 2015, Том: 640, Страницы: 94-100 Страниц : 7 DOI: 10.1016/j.cplett.2015.10.016
Ключевые слова WATER OXIDATION; PAIRED ORBITALS; HYDROXYLATION; CATALYSTS; DIOXYGEN; COMPLEXES; DENSITY; BOND; DETERMINANT; CONVERSION
Авторы Shubin Aleksandr A. 1 , Ruzankin Sergey Ph. 1 , Zilberberg Igor L. 1 , Parmon Valentin N. 1
Организации
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Prospekt Akademika Lavrentieva 5, Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Российский научный фонд 14-13-01155

Реферат: The abstraction of hydrogen from methane on the terminal iron-oxo group in the ferryl FeIVdouble bond; length as m-dashO and oxyl FeIIIsingle bondOradical dot states, the hydrogen peroxide group Fesingle bondOOH and the peroxo group Fesingle bondOOsingle bondFe created in iron hydroxide was modeled by means of the density functional theory. The active groups were built using the Fe4O4(OH)4 starting complex having one hydrogen removed imitating the effect of the external oxidizer. Among considered groups the oxyl group is predicted to have the highest reactivity. A clear distinction in reactivity between the FeIIIsingle bondOradical dot and FeIVdouble bond; length as m-dashO quasi-degenerate states has been attributed to the sign of terminal oxygen spin polarization.
Библиографическая ссылка: Shubin A.A. , Ruzankin S.P. , Zilberberg I.L. , Parmon V.N.
Distinct Activity of the Oxyl Fe(III) -O Group in the Methane Dissociation by Activated Iron Hydroxide: DFT Predictions
Chemical Physics Letters. 2015. V.640. P.94-100. DOI: 10.1016/j.cplett.2015.10.016 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 28 июл. 2015 г.
Принята к публикации: 8 окт. 2015 г.
Опубликована online: 23 окт. 2015 г.
Опубликована в печати: 1 нояб. 2015 г.
Идентификаторы БД:
Web of science: WOS:000365814500018
Scopus: 2-s2.0-84946039559
РИНЦ: 24968224
Chemical Abstracts: 2015:1674911
Chemical Abstracts (print): 163:666098
OpenAlex: W2180814668
Цитирование в БД:
БД Цитирований
Web of science 11
Scopus 11
РИНЦ 12
OpenAlex 15
Альметрики: