Perfluorinated resinsulphonic acid (Nafion-H1) catalyzed highly efficient oxidations of organic compounds with hydrogen peroxide
IR@IIP: CSIR-Indian Institute of Petroleum, Dehradun
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Creator |
Jain, Suman L
Sain, Bir |
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Date |
2009-06-12T10:32:23Z
2009-06-12T10:32:23Z 2009-06-12T10:32:23Z |
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Identifier |
http://hdl.handle.net/123456789/145
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Description |
Perfluorinated resinsulphonic acid (Nafion-H1) was found to be highly efficient, environmentally friendly, recyclable heterogeneous catalyst
for the oxidation of sulphides to sulphones, tertiary amines to N-oxides, secondary alcohols to esters/lactones and aldehydes to methyl esters in
excellent yields under mild reaction conditions using 30% hydrogen peroxide as an oxidant. Alkyl sulphides in general were found to be more
reactive than aryl sulphides. Similarly, aliphatic tertiary amines and pyridines substituted with electron donating groups were found to be more
reactive. Among the various secondary alcohols and aldehydes studied, alicyclic alcohols and substituted benzaldehydes were found to be more
reactive. Acetonitrile and 1,2-dichloroethane were found to be the most suitable solvents for these transformations.
# 2005 Elsevier B.V. All rights reserved.
Keywords: Nafion; Oxidation; Hydrogen peroxide; Perfluorinated resinsulphonic acid; Heterogeneous catalysis
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Language |
en_US
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Subject |
Hydrogen Peroxide
Oxidation |
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Title |
Perfluorinated resinsulphonic acid (Nafion-H1) catalyzed highly efficient oxidations of organic compounds with hydrogen peroxide
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Type |
Article
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