Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media
The kinetics of oxidation of some organic diols by tripropylammonium fluorochromate (TriPAFC) have been studied in dimethylsulfoxide (DMSO). The main product of oxidation is the corresponding hydroxy aldehydes. The reaction is first order with respect to TriPAFC and exhibited Michaelis-Menten type k...
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doaj-4fcee516a5fb471fb180d69a8480e84f2020-11-24T22:29:38ZengElsevierArabian Journal of Chemistry1878-53522016-09-019S1S602S60910.1016/j.arabjc.2011.07.004Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous mediaS. Sheik Mansoor0S. Syed Shafi1Post Graduate and Research Department of Chemistry, C. Abdul Hakeem College, Melvisharam 632 509, Tamil Nadu, IndiaPost Graduate and Research Department of Chemistry, Thiruvalluvar University, Vellore 635 106, Tamil Nadu, IndiaThe kinetics of oxidation of some organic diols by tripropylammonium fluorochromate (TriPAFC) have been studied in dimethylsulfoxide (DMSO). The main product of oxidation is the corresponding hydroxy aldehydes. The reaction is first order with respect to TriPAFC and exhibited Michaelis-Menten type kinetics with respect to organic diols. The reaction is catalyzed by hydrogen ions. The hydrogen ion dependence has the form: kobs = a + b[H+]. Various thermodynamic parameters for the oxidation have been reported and discussed along with the validity of isokinetic relationship. Oxidation of diols was studied in 18 different organic solvents. The rate data are showing satisfactory correlation with Kamlet–Taft solvotochromic parameters (α, β and π∗). A suitable mechanism of oxidation has been proposed.http://www.sciencedirect.com/science/article/pii/S1878535211001870Tripropylammonium fluorochromateDiolsSolvent effectKinetics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S. Sheik Mansoor S. Syed Shafi |
spellingShingle |
S. Sheik Mansoor S. Syed Shafi Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media Arabian Journal of Chemistry Tripropylammonium fluorochromate Diols Solvent effect Kinetics |
author_facet |
S. Sheik Mansoor S. Syed Shafi |
author_sort |
S. Sheik Mansoor |
title |
Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media |
title_short |
Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media |
title_full |
Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media |
title_fullStr |
Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media |
title_full_unstemmed |
Correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media |
title_sort |
correlation analysis of reactivity in the oxidation of some organic diols by tripropylammonium fluorochromate in non-aqueous media |
publisher |
Elsevier |
series |
Arabian Journal of Chemistry |
issn |
1878-5352 |
publishDate |
2016-09-01 |
description |
The kinetics of oxidation of some organic diols by tripropylammonium fluorochromate (TriPAFC) have been studied in dimethylsulfoxide (DMSO). The main product of oxidation is the corresponding hydroxy aldehydes. The reaction is first order with respect to TriPAFC and exhibited Michaelis-Menten type kinetics with respect to organic diols. The reaction is catalyzed by hydrogen ions. The hydrogen ion dependence has the form: kobs = a + b[H+]. Various thermodynamic parameters for the oxidation have been reported and discussed along with the validity of isokinetic relationship. Oxidation of diols was studied in 18 different organic solvents. The rate data are showing satisfactory correlation with Kamlet–Taft solvotochromic parameters (α, β and π∗). A suitable mechanism of oxidation has been proposed. |
topic |
Tripropylammonium fluorochromate Diols Solvent effect Kinetics |
url |
http://www.sciencedirect.com/science/article/pii/S1878535211001870 |
work_keys_str_mv |
AT ssheikmansoor correlationanalysisofreactivityintheoxidationofsomeorganicdiolsbytripropylammoniumfluorochromateinnonaqueousmedia AT ssyedshafi correlationanalysisofreactivityintheoxidationofsomeorganicdiolsbytripropylammoniumfluorochromateinnonaqueousmedia |
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