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AN in situ13C MAS NMR study of the zeolite-catalyzed alkylation of polar aromatics Научная публикация

Конференция 14th International Zeolite Conference
25-30 апр. 2004 , Cape Town
Журнал Studies in Surface Science and Catalysis
ISSN: 0167-2991
Вых. Данные Год: 2004, Том: 154. Part C, Страницы: 2221-2227 Страниц : 7 DOI: 10.1016/s0167-2991(04)80479-8
Авторы Ivanova I.I. 1 , Pomakhina E.B. 1 , Borodina I.B. 1 , Rebrov A.I. 2 , Wang W. 3 , Weitkamp J. 3 , Hunger M. 3
Организации
1 Lomonosov Moscow State University
2 Topchiev Institute of Petrochemical Synthesis RAS
3 University of Stuttgart
Реферат: In situ13C MAS NMR was applied to study the mechanisms of the N-alkylation of aniline and of the O-alkylation of phenol with methanol on acidic (H-Y) and basic (CsOH/CsNa-Y) zeolite Y catalysts. Methanol-13C was the labeled reactant. The results point to similar mechanisms of the N- and O-alkylation on Brønsted acid sites including a dehydration of methanol towards dimethyl ether (DME) or surface methoxy groups, which further react with aniline to N-methyalnilinium, N,N-dimethylanilinium, and N,N, N-trimethylanilinium cations or a direct reaction of phenol and methanol towards anisole. At variance, different mechanistic pathways were observed on basic zeolite Y: N-alkylation is shown to proceed via methanol dehydrogenation leading to the formation of formaldehyde species responsible for further methylation, while O-alkylation includes the formation of phenolate ions initiating the alkylation reaction.
Библиографическая ссылка: Ivanova I.I. , Pomakhina E.B. , Borodina I.B. , Rebrov A.I. , Wang W. , Weitkamp J. , Hunger M.
AN in situ13C MAS NMR study of the zeolite-catalyzed alkylation of polar aromatics
Studies in Surface Science and Catalysis. 2004. V.154. Part C. P.2221-2227. DOI: 10.1016/s0167-2991(04)80479-8 Scopus OpenAlex
Идентификаторы БД:
Scopus: 2-s2.0-11844249332
OpenAlex: W1536693421
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OpenAlex 4
Scopus 4
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