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Peng C, Wang H, Hu P. Theoretical insights into how the first C-C bond forms in the methanol-to-olefin process catalysed by HSAPO-34. Phys Chem Chem Phys. 2016;18(21):14495-502doi: 10.1039/c5cp08029k.
Peng, C., Wang, H., & Hu, P. (2016). Theoretical insights into how the first C-C bond forms in the methanol-to-olefin process catalysed by HSAPO-34. Physical chemistry chemical physics : PCCP, 18(21), 14495-502. https://doi.org/10.1039/c5cp08029k
Peng, Chao, et al. "Theoretical insights into how the first C-C bond forms in the methanol-to-olefin process catalysed by HSAPO-34." Physical chemistry chemical physics : PCCP vol. 18,21 (2016): 14495-502. doi: https://doi.org/10.1039/c5cp08029k
Peng C, Wang H, Hu P. Theoretical insights into how the first C-C bond forms in the methanol-to-olefin process catalysed by HSAPO-34. Phys Chem Chem Phys. 2016 May 25;18(21):14495-502. doi: 10.1039/c5cp08029k. PMID: 27173579.
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Phys Chem Chem Phys. 2016 May 25;18(21):14495-502. doi: 10.1039/c5cp08029k.

Theoretical insights into how the first C-C bond forms in the methanol-to-olefin process catalysed by HSAPO-34.

Physical chemistry chemical physics : PCCP

Chao Peng, Haifeng Wang, P Hu

Affiliations

  1. Key Laboratory for Advanced Materials, Centre for Computational Chemistry and Research Institute of Industrial Catalysis, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China. [email protected].
  2. Key Laboratory for Advanced Materials, Centre for Computational Chemistry and Research Institute of Industrial Catalysis, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China. [email protected] and School of Chemistry and Chemical Engineering, The Queen's University of Belfast, Belfast BT9 5AG, UK. [email protected].

PMID: 27173579 DOI: 10.1039/c5cp08029k

Abstract

We report here a comprehensive understanding of the first C-C coupling during the induction period of the methanol-to-olefin process using density functional theory with the HSE06 hybrid functional. We illustrate the possible routes of formation for the active carbenium ion (CH3OCH2(+)), which has been identified to play an important part in triggering the formation of the first C-C bond and the hydrocarbon pool species. CH3OCH2(+) can be generated not only from dimethyl ether and Z(O)-CH3, but also from the reaction of HCHO and Z(O)-CH3, which has a lower effective barrier. An understanding of the dominance of CH3OCH2(+) over other carbocations and direct C-C coupling pathways is presented and quantitatively analysed. The charge distribution in the formation of CH3OCH2(+) is revealed and it is confirmed that the carbenium ion is thermodynamically more favoured than the radical. The subsequent reaction after the first C-C coupling was investigated, which uncovered some important active C2 species that possibly led to the formation of the active hydrocarbon pool intermediates and may finally realize the catalytic cycle.

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