Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis
Kinetics of the oxidation of primary aliphatic alcohols has been carried out using phase transferred monochromate in benzene. Tetrabutylammonium bromide (TBAB) and tetrabutylphosphonium bromide (TBPB) are used as phase transfer catalysts (PT catalyst). The reaction shows first order dependence on bo...
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Growing Science
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doaj-7376180148fe429b91f2dcfcd685e3602020-11-25T00:13:57ZengGrowing ScienceCurrent Chemistry Letters1927-72961927-730X2014-03-013210911410.5267/j.ccl.2013.12.001Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysisK. BijudasT. D. Radhakrishnan NairKinetics of the oxidation of primary aliphatic alcohols has been carried out using phase transferred monochromate in benzene. Tetrabutylammonium bromide (TBAB) and tetrabutylphosphonium bromide (TBPB) are used as phase transfer catalysts (PT catalyst). The reaction shows first order dependence on both [alcohol] and [monochromate ion]. The oxidation leads to the formation of corresponding aldehyde and no traces of carboxylic acid has been detected. The reaction mixture failed to induce the polymerization of added acrylonitrile which rules out the presence radical intermediates in the reaction. Various thermodynamic parameters have been evaluated and a suitable mechanism has been proposed.http://www.growingscience.com/ccl/Vol3/ccl_2013_29.pdfSelective oxidationPhase transfer catalysisKineticsMechanismPhase transferred monochromate |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
K. Bijudas T. D. Radhakrishnan Nair |
spellingShingle |
K. Bijudas T. D. Radhakrishnan Nair Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis Current Chemistry Letters Selective oxidation Phase transfer catalysis Kinetics Mechanism Phase transferred monochromate |
author_facet |
K. Bijudas T. D. Radhakrishnan Nair |
author_sort |
K. Bijudas |
title |
Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis |
title_short |
Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis |
title_full |
Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis |
title_fullStr |
Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis |
title_full_unstemmed |
Kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis |
title_sort |
kinetics and mechanism of the selective oxidation of primary aliphatic alcohols under phase transfer catalysis |
publisher |
Growing Science |
series |
Current Chemistry Letters |
issn |
1927-7296 1927-730X |
publishDate |
2014-03-01 |
description |
Kinetics of the oxidation of primary aliphatic alcohols has been carried out using phase transferred monochromate in benzene. Tetrabutylammonium bromide (TBAB) and tetrabutylphosphonium bromide (TBPB) are used as phase transfer catalysts (PT catalyst). The reaction shows first order dependence on both [alcohol] and [monochromate ion]. The oxidation leads to the formation of corresponding aldehyde and no traces of carboxylic acid has been detected. The reaction mixture failed to induce the polymerization of added acrylonitrile which rules out the presence radical intermediates in the reaction. Various thermodynamic parameters have been evaluated and a suitable mechanism has been proposed. |
topic |
Selective oxidation Phase transfer catalysis Kinetics Mechanism Phase transferred monochromate |
url |
http://www.growingscience.com/ccl/Vol3/ccl_2013_29.pdf |
work_keys_str_mv |
AT kbijudas kineticsandmechanismoftheselectiveoxidationofprimaryaliphaticalcoholsunderphasetransfercatalysis AT tdradhakrishnannair kineticsandmechanismoftheselectiveoxidationofprimaryaliphaticalcoholsunderphasetransfercatalysis |
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1725392197371559936 |