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Mobility of Stable pi-Complexes of Ethylene with Ag+ Cations in Ag/H-ZSM-5 Zeolite: A H-2 Solid-State NMR Study Научная публикация

Журнал The Journal of Physical Chemistry C
ISSN: 1932-7447 , E-ISSN: 1932-7455
Вых. Данные Год: 2016, Том: 120, Номер: 9, Страницы: 4993-5000 Страниц : 8 DOI: 10.1021/acs.jpcc.5b12687
Ключевые слова Light polarization; Methane; Molecules; Nuclear magnetic resonance spectroscopy; Positive ions; Rotation; Silver; Zeolites
Авторы Kolokolov Daniil I. 1,2 , Arzumanov Sergei S. 1,2 , Freude Dieter 3 , Haase Juerger 3 , Stepanov Alexander G. 1,2
Организации
1 Boreskov Institute of Catalysis, Siberian Branch of Russian Academy of Sciences, Prospekt Akademika Lavrentieva 5, Novosibirsk 630090, Russia
2 Faculty of Natural Sciences, Department of Physical Chemistry, Novosibirsk State University, Pirogova Street 2, Novosibirsk 630090, Russia
3 Fakultat fur Physik und Geowissenschaften, Universitat Leipzig, Linne ̈ straße 5, 04103 Leipzig, Germany

Информация о финансировании (3)

1 Федеральное агентство научных организаций России V.44.2.11.
2 Российский фонд фундаментальных исследований 14-03-91333
3 German Research Foundation HA 1893/16

Реферат: Ethylene has-been established to form stable pi-complexes with Ag+ cations in Ag-modified zeolite H-ZSM-5 (Ag/H-ZSM-5), which strongly affect the reactivity of ethylene on this catalyst. With the aim Of revealing the catalytic and adsorptive properties of Ag+ cations in Ag/H-ZSM-5, a characterization of the mobility of ethylene pi-complex, located in the zeolite pores, has been performed with H-2 solid-state NMR spectroscopy. Ethylene molecules were established to remain bound to the Ag+ cations at temperatures up to 556 K. In the bound state, ethylene exhibits a H-2 NMR line shape typical for anisotropic motions. It is inferred that being adsorbed on Ag+ cation, ethylene molecule is involved in two internal rotations about its symmetry axes: along the C-2 axis aligned with the C=C bond and about the second C-2' axis orthogonal to the molecule plane. The first rotation occurs with the rate, k(1), of 10-40 kHz and activation barrier E-1 = 2.3 kJ mol(-1), while the second motion occurs with the rate k(2) of 10-400 kHz and E-2 = 4.7 kJ mol(-1). The latter motion is faster than the former One. Both motions occur by four-site jump exchange mechanism. When methane is coadsorbed on the zeolite, the dynamical picture becomes different within two different temperature regions, with T <= 392 K and T > 392 K. Below 392 K, the rotation mechanism is similar to that without methane coadsortion. However, the barrier for the rotation about the C-2' axis increases (E-2(II) = 7.4 kJ mol(-1)), which is evidence for the methane interaction with the ethylene pi-complex. At temperatures as high as 392 K, the 2H NMR line shape of adsorbed ethylene becomes typical for isotropic-like motion. The barrier of the motion, E = 25 kJ mol(-1), is accounted for by involvement of ethylene in the presence of methane in some isotropic or translational motions. At T >= 491 K, the line shape analysis reveals an H/D exchange between C2D4 and CH4.
Библиографическая ссылка: Kolokolov D.I. , Arzumanov S.S. , Freude D. , Haase J. , Stepanov A.G.
Mobility of Stable pi-Complexes of Ethylene with Ag+ Cations in Ag/H-ZSM-5 Zeolite: A H-2 Solid-State NMR Study
The Journal of Physical Chemistry C. 2016. V.120. N9. P.4993-5000. DOI: 10.1021/acs.jpcc.5b12687 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 29 дек. 2015 г.
Принята к публикации: 16 февр. 2016 г.
Опубликована online: 26 февр. 2016 г.
Опубликована в печати: 10 мар. 2016 г.
Идентификаторы БД:
Web of science: WOS:000372042600030
Scopus: 2-s2.0-84961118098
РИНЦ: 27098799
Chemical Abstracts: 2016:283645
Chemical Abstracts (print): 164:338419
OpenAlex: W2280978860
Цитирование в БД:
БД Цитирований
Web of science 12
Scopus 13
РИНЦ 12
OpenAlex 13
Альметрики: