Theoretical Chemistry Accounts

, Volume 127, Issue 1, pp 39–47

Solvolysis process of organophosphorus compound P-[2-(dimethylamino)ethyl]-N,N-dimethylphosphonamidic fluoride with simple and α-nucleophiles: a DFT study

  • Manoj K. Kesharwani
  • Md. Abdul Shafeeuulla Khan
  • Tusar Bandyopadhyay
  • Bishwajit Ganguly
Regular Article

DOI: 10.1007/s00214-009-0701-2

Cite this article as:
Kesharwani, M.K., Khan, M.A.S., Bandyopadhyay, T. et al. Theor Chem Acc (2010) 127: 39. doi:10.1007/s00214-009-0701-2

Abstract

Density functional theory (DFT) has been used to study the solvolysis process of the organophosphorus compound P-[2-(dimethylamino)ethyl]-N,N-dimethylphosphonamidic fluoride (GV) with simple nucleophile [hydroxide (HO)] and α-nucleophiles [hydroperoxide (HOO) and hydroxylamine anion (NH2O)]. The lowest energy conformer of GV used for the solvolysis process was identified with Monte Carlo conformational search (MCMM) algorithm employing MMFFs force field followed by DFT calculations. The profound effect was found for α-nucleophiles toward the solvolysis of GV compared to normal alkaline hydrolysis. Incorporation of solvent (water) employing SCRF (PCM) model at B3LYP/6-31+G* showed that solvolysis of GV with hydroperoxide (activation energy = 7.6 kcal/mol) is kinetically more favored compared to hydroxide and hydroxylamine anion (activation energy = 11.0 and 9.2 kcal/mol, respectively). The faster solvolysis of GV with hydroperoxide is achieved due to strong intermolecular hydrogen bonding in the transition state geometry compared to similar α-nucleophile hydroxylamine anion. Assistance of a water molecule in solvolysis of GV affects the activation barriers; however, the hydroperoxidolysis remains the preferential process. The topological properties of electron density distributions for (–X–H···O, X = O, N) intermolecular hydrogen bonding bridges have been analyzed in terms of Bader theory of atoms in molecules (AIM). Further, the analysis was extended by natural bond orbital (NBO) methods for the strength of intermolecular hydrogen bonding in the transition state geometries. This study showed that the reactivity of these α-nucleophiles toward the solvolysis of GV is a delicate balance between the nucleophilicity and hydrogen-bond strength. Solvation governs the overall thermodynamics for the destruction of GV, which otherwise is unfavored in the gas phase studies.

Keywords

Solvolysis Ab initio calculations α-Nucleophiles Nerve agent Hydroxylamine anion 

Supplementary material

214_2009_701_MOESM1_ESM.doc (700 kb)
Supplementary material 1 (DOC 700 kb)

Copyright information

© Springer-Verlag 2009

Authors and Affiliations

  • Manoj K. Kesharwani
    • 1
  • Md. Abdul Shafeeuulla Khan
    • 1
  • Tusar Bandyopadhyay
    • 2
  • Bishwajit Ganguly
    • 1
  1. 1.Analytical Science DisciplineCentral Salt and Marine Chemicals Research Institute (Council of Scientific and Industrial Research)BhavnagarIndia
  2. 2.Theoretical Chemistry Section, Chemistry GroupBhabha Atomic Research CentreTrombay, MumbaiIndia

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