Response to Comment on “Activation of methane to CH 3 + : A selective industrial route to methanesulfonic acid”

Author:

Díaz-Urrutia Christian1ORCID,Ott Timo1ORCID

Affiliation:

1. R&D Department, Chemical Division, Grillo-Werke AG, 47169 Duisburg, Germany.

Abstract

Roytman and Singleton argue that our proposed electrophilic mechanism for the sulfonation of methane in superacid conditions is “not plausible.” We clarify certain terms that might have caused misinterpretation of our proposed mechanism and supplement the discussion. We reaffirm that an electrophilic mechanism may be operative under our reaction conditions.

Funder

Grillo-Werke AG

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference14 articles.

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

2. Making more from methane

3. G. A. Olah G. K. S. Prakash A. Molnar S. Sommer Superacid Chemistry (Wiley ed. 2 2009). For the composition of oleum of sulfuric acid see Chapter 2.2.2.1; for the nonclassical carbocation CH 5 + and its reactivity see Chapter 3.5; for oxonium ions see Chapter 4.2.1; for oxenium ions see Chapter 4.3.4.1.

4. Homogeneous Functionalization of Methane

5. Oxyfunctionalization of hydrocarbons. 4. Fluorosulfuric acid-antimony pentafluoride, fluorosulfuric acid, sulfuric acid, and hydrofluoric acid induced electrophilic oxygenation of alkanes with hydrogen peroxide

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