Solvolysis of organophosphorus pesticide parathion with simple and α nucleophiles: a theoretical study View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2017-07-01

AUTHORS

Chandan Sahu, Abhijit K Das

ABSTRACT

Density functional theory (DFT) has been used to study the solvolysis process of the organophosphorus compound, O,O-diethyl p-nitrophenyl thiophosphate (Parathion, PTH) with α\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\upalpha $$\end{document}-nucleophiles [hydroxylamine anion (NH2O-\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\hbox {NH}_{2}\hbox {O}^{-}$$\end{document}), hydroperoxide (HOO-\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\hbox {HOO}^{-}$$\end{document}) and simple nucleophile methylthiolate (CH3S-\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\hbox {CH}_{3}\hbox {S}^{-}$$\end{document}) in both gas and aqueous phases. Formation of a trigonal bipyramidal intermediate at the phosphorus center followed by elimination of leaving group is considered to be the major solvolyzed pathway through addition-elimination scheme. In this study, although there are two possible orientations for incoming nucleophiles with respect to the substrate, the present reaction mechanism is found to be independent of this relative orientation. The proposed addition-elimination mechanism has been first explored here. The results indicate that the α\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\upalpha $$\end{document}-effect is observed in presence of solvent. Free energy barriers for NH2O-\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\hbox {NH}_{2}\hbox {O}^{-}$$\end{document} and HOO-\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\hbox {HOO}^{-}$$\end{document} are comparable and lower than that for the simple nulcleophile, CH3S-\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\hbox {CH}_{3}\hbox {S}^{-}$$\end{document}. An important physical insight of this study is that there is a significant influence of the reaction medium on the nucleophilic reaction for solvolysis of PTH irrespective of the relative orientation of incoming nucleophile group.Graphical Abstract Synopsis: Computational study of solovolysis of toxic organophosphorus pesticide, parathion by anionic nucleophiles has been reported in both gas and aqueous phase. The results suggest that there is significance effect of the medium on the mechanism and this reaction mechanism is independent of orientation of incoming nucleophiles. More... »

PAGES

1301-1317

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s12039-017-1322-2

DOI

http://dx.doi.org/10.1007/s12039-017-1322-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1090325673


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