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Direct Mechanism of the First Carbon–Carbon Bond Formation in the Methanol‐to‐Hydrocarbons Process
Author(s) -
Wu Xinqiang,
Xu Shutao,
Zhang Wenna,
Huang Jindou,
Li Jinzhe,
Yu Bowen,
Wei Yingxu,
Liu Zhongmin
Publication year - 2017
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201703902
Subject(s) - methanol , dimethyl ether , chemistry , catalysis , carbon–carbon bond , breakage , zeolite , reaction mechanism , ether , carbon fibers , photochemistry , organic chemistry , materials science , composite material , composite number
In the past two decades, the reaction mechanism of C−C bond formation from either methanol or dimethyl ether (DME) in the methanol‐to‐hydrocarbons (MTH) process has been a highly controversial issue. Described here is the first observation of a surface methyleneoxy analogue, originating from the surface‐activated DME, by in situ solid‐state NMR spectroscopy, a species crucial to the first C−C bond formation in the MTH process. New insights into the first C−C bond formation were provided, thus suggesting DME/methanol activation and direct C−C bond formation by an interesting synergetic mechanism, involving C−H bond breakage and C−C bond coupling during the initial methanol reaction within the chemical environment of the zeolite catalyst.

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