Oxidative ammonolysis of 3,4-dimethylpyridine on the vanadium oxide catalysts

Oxidative ammonolysis of 3,4-dimethylpyridine on an individual vanadium oxide (V2O5) catalyst and binary vanadium oxide catalysts, modified by additions of SnO2 and ZrO2, has been studied. A connection between СН- acidity of the methyl groups of the substrate in the gaseous phase and in the chemosor...

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Bibliographic Details
Main Authors: Vorobyev Pavel, Serebryanskaya Anna, Yugay Olga, Mikhailovskaya Tatyana
Format: Article
Language:English
Published: Serbian Chemical Society 2020-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2020/0352-51391900107V.pdf
Description
Summary:Oxidative ammonolysis of 3,4-dimethylpyridine on an individual vanadium oxide (V2O5) catalyst and binary vanadium oxide catalysts, modified by additions of SnO2 and ZrO2, has been studied. A connection between СН- acidity of the methyl groups of the substrate in the gaseous phase and in the chemosorbed state and the sequence of their transformation into a cyano group has been established. It has been shown that nucleophilicity of vanadyl oxygen, calculated by the Density Functional Theory method, increases with V2O5 modification by SnO2 and ZrO2 additions. Herewith, an increasing yield of 3- methyl-4-cyanopyridine and imide of pyridine-3,4-dicarboxylic acid was observed. A proposed mechanism of the imide of pyridine-3,4-dicarboxylic acid formation has been discussed
ISSN:0352-5139
1820-7421