Issue 66, 2019

Efficient catalytic oxidation of methyl aromatic hydrocarbon with N-alkyl pyridinium salts

Abstract

A series of N-alkyl pyridinium salts were synthesized and employed as metal-free catalyst for the selective oxidation of methyl aromatic hydrocarbon with molecular oxygen. The electronic effect of the substitutes was found to be an important factor for the catalytic performance. With the introduction of electron-donating substitute –N(CH3)2, the conversion of p-xylene and selectivity of p-toluic acid could be simultaneously increased. 1-Benzyl-4-N,N-dimethylaminopyridinium salt showed the highest catalytic activity, and 95% conversion with 84% of selectivity to p-toluic acid could be obtained for the selective oxidation of p-xylene. Several methyl aromatic hydrocarbons could all be efficiently oxidized with the reported catalyst at the absence of any metal species.

Graphical abstract: Efficient catalytic oxidation of methyl aromatic hydrocarbon with N-alkyl pyridinium salts

Supplementary files

Article information

Article type
Paper
Submitted
09 Oct 2019
Accepted
07 Nov 2019
First published
26 Nov 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 38891-38896

Efficient catalytic oxidation of methyl aromatic hydrocarbon with N-alkyl pyridinium salts

Q. Zhang, H. He, H. Wang, Z. Zhang and C. Chen, RSC Adv., 2019, 9, 38891 DOI: 10.1039/C9RA08185B

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements