Literature DB >> 30898928

Activation of methane to CH3 +: A selective industrial route to methanesulfonic acid.

Christian Díaz-Urrutia1, Timo Ott2.   

Abstract

Direct methane functionalization to value-added products remains a challenge because of the propensity for overoxidation in many reaction environments. Sulfonation has emerged as an attractive approach for achieving the necessary selectivity. Here, we report a practical process for the production of methanesulfonic acid (MSA) from only two reactants: methane and sulfur trioxide. We have achieved >99% selectivity and yield of MSA. The electrophilic initiator based on a sulfonyl peroxide derivative is protonated under superacidic conditions, producing a highly electrophilic oxygen atom capable of activating a C-H bond of methane. Mechanistic studies support the formation of CH3 + as a key intermediate. This method is readily scalable with reactors connected in series for prospective production of up to 20 metric tons per year of MSA.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

Entities:  

Year:  2019        PMID: 30898928     DOI: 10.1126/science.aav0177

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  2 in total

1.  Ambient methane functionalization initiated by electrochemical oxidation of a vanadium (V)-oxo dimer.

Authors:  Jiao Deng; Sheng-Chih Lin; Jack Fuller; Jesus A Iñiguez; Danlei Xiang; Di Yang; Gary Chan; Hao Ming Chen; Anastassia N Alexandrova; Chong Liu
Journal:  Nat Commun       Date:  2020-07-23       Impact factor: 14.919

2.  Water enables mild oxidation of methane to methanol on gold single-atom catalysts.

Authors:  Laihao Luo; Jie Luo; Hongliang Li; Fangning Ren; Yifei Zhang; Andong Liu; Wei-Xue Li; Jie Zeng
Journal:  Nat Commun       Date:  2021-02-22       Impact factor: 14.919

  2 in total

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