Formation Mechanism of the First Carbon–Carbon Bond and the First Olefin in the Methanol Conversion into Hydrocarbons. (1st April 2016)

• Record Type: Journal Article
• Authors: Liu, Yue; Müller, Sebastian; Berger, Daniel; Jelic, Jelena; Reuter, Karsten; Tonigold, Markus; Sanchez‐Sanchez, Maricruz; Lercher, Johannes A.
• Is Part Of: Angewandte Chemie. Volume 128:Number 19(2016)
• Page Start: 5817
• Page End: 5820
• Publication Date: 2016-04-01
• Subjects: Carbonylierungen -- C-C-Kupplungen -- Methanol-zu-Kohlenwasserstoffen -- Olefine -- Zeolithe; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201511678
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: The elementary reactions leading to the formation of the first carbon–carbon bond during early stages of the zeolite‐catalyzed methanol conversion into hydrocarbons were identified by combining kinetics, spectroscopy, and DFT calculations. The first intermediates containing a C−C bond are acetic acid and methyl acetate, which are formed through carbonylation of methanol or dimethyl ether even in presence of water. A series of acid‐catalyzed reactions including acetylation, decarboxylation, aldol condensation, and cracking convert those intermediates into a mixture of surface bounded hydrocarbons, the hydrocarbon pool, as well as into the first olefin leaving the catalyst. This carbonylation based mechanism has an energy barrier of 80 kJ mol −1 for the formation of the first C−C bond, in line with a broad range of experiments, and significantly lower than the barriers associated with earlier proposed mechanisms.