Metadata of CSIR Papers
View Archive Info| Field | Value | |
| Creator |
Kesharwani, MK
Khan, MAS Bandyopadhyay, T Ganguly, B |
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| Subject |
Chemistry
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| Description |
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 alpha-nucleophiles [hydroperoxide (HOO(-)) and hydroxylamine anion (NH(2)O(-))]. 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 alpha-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 alpha-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 center dot center dot center dot 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 alpha-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.
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| Publisher |
SPRINGERNEW YORK233 SPRING ST, NEW YORK, NY 10013 USA
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| Date |
2011-09-20T12:03:12Z
2011-09-20T12:03:12Z 2010 |
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| Type |
Article
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| Identifier |
THEORETICAL CHEMISTRY ACCOUNTS
1432-881X http://hdl.handle.net/123456789/12215 |
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| Language |
English
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