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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Main Authors: S. Sheik Mansoor, S. Syed Shafi
Format: Article
Language:English
Published: Elsevier 2016-09-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535211001870
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spelling 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
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AT ssyedshafi correlationanalysisofreactivityintheoxidationofsomeorganicdiolsbytripropylammoniumfluorochromateinnonaqueousmedia
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