Chemical Engineering and Science
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Chemical Engineering and Science. 2013, 1(2), 17-21
DOI: 10.12691/ces-1-2-1
Open AccessArticle

Semi-Empirical Evaluation of the Probability of Structural Rearrangements in Nitrone Spin Traps

F. N. Dultsev, and G. G. Dultseva

Pub. Date: April 07, 2013

Cite this paper:
F. N. Dultsev and G. G. Dultseva. Semi-Empirical Evaluation of the Probability of Structural Rearrangements in Nitrone Spin Traps. Chemical Engineering and Science. 2013; 1(2):17-21. doi: 10.12691/ces-1-2-1

Abstract

Structural rearrangements induced by the action of oxidizers in nitrone spin traps are investigated by means of the semi-empirical calculation of energy changes that accompany the processes assumed on the basis of experimental observations. The mechanisms of cyclization of acyclic nitrones and cycle opening in cyclic dinitrones are assumed on the basis of calculation results. It is shown that water as a solvent plays an important part in these structural rearrangements. Semi-empirical prediction of the reactivity of nitrones as spin traps in oxidative environments is demonstrated to be helpful as a preliminary step to study the spin-trapping capacity of various substituted nitrones.

Keywords:
spin trapping semi-empirical simulation cyclization nitrone

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References:

[1]  Janzen, E.G., Spin Trapping. Accounts Chem. Res. 4 (1971) 31-40.
 
[2]  Perkins, M.R., Spin Trapping. Adv. Phys. Org. Chem. 17 (1981) 1.
 
[3]  Zubarev, V.E., Spin Trapping. Applications in Chemistry, Biology and Medicine. Moscow, MSU Publishers, 1985.
 
[4]  Fleming, J., Grenzorbitale und Reaktionen organischer erbindungen. N.Y.: Chem.-Verl. 1979.
 
[5]  Dultsev, F.N., Structure of adsorption complex: Modeling and experiment. Journ. Structur. Chem. 47 (2006) 575.
 
[6]  Dultsev, F.N., Dultseva, G.G. Predictive capacity of semi-empirical MNDO/PM3 and molecular mechanics MM2 estimations of the reactivity of cyclic nitrones as spin traps. Chem. Phys. Lett. 429 (2006) 445.
 
[7]  Skubnevskaya, G.I., Dultseva, G.G., Shchukin, G.I., Volodarsky, L.B., Effect of pH on EPR spectra of the radical adducts of new spin trap 1,2,2,5,5-pentamethyl-3-imidazoline-3-oxide. Izv. AN SSSR ser. khimich. 2 (1987) 312.
 
[8]  Dultseva, G.G., Skubnevskaya, G.I., Volodarsky, L.B., Dulepova, N.V., Tikhonov, A.Ya., New spin traps: 2,3-dihydropyrazine-1,4-dioxides – cyclic conjugated α-dinitrones and α-phenylnitrones with functional groups. Izv. Sib. Otd. Akad. Nauk. Ser. Khim. Nauk, 1 (1989) 77.
 
[9]  Dultseva, G.G., Skubnevskaya, G.I., Tikhonov, A.Ya., Mazhukin, D.G., Volodarsky, L.B., Derivatives of dihydropyrazine-1,4-dioxide, 3-imidazoline 3-oxide and alpha-phenyl nitrones with functional groups as new spin traps in solution and in the gas phase. J. Phys. Chem. 100 (1996) 17523.
 
[10]  Dewar, M.J.S., Thiel, W.J., Ground states of molecules. 38. The MNDO method: approximations and parameters. Amer. Chem. Soc. 99 (1977) 4899.
 
[11]  Dewar, M.J.S., Zoebisch, E.G., Healy, E.F., Stewart, J.J.P., The development and use ofquantum mechanical molecular models. 76. AMI: a new general purpose quantum mechanical molecular model. J. Am. Chem. Soc. 107 (1985) 3902.
 
[12]  Zemel, H., Fessenden, R.W., Electron spin resonance studies of phenyl and pyridyl radicals in aqueous solution. J. Phys. Chem. 79 (1975) 1419.
 
[13]  Harbour, J.R., Chow, V., An Electron Spin Resonance Study of the Spin Adducts of OH and HOz Radicals with Nitrones in the Ultraviolet Photolysis of Aqueous Hydrogen Peroxide Solutions. Can. J. Chem. 52 (1974) 3549.
 
[14]  Wink, D.A., Desrosiers, M., Unusual spin-trap chemistry for the reaction of hydroxyl radical with the carcinogen N-nitrosodimethylamine. Radiat. Phys. Chem. 38 (1991) 467.
 
[15]  Joule, J.A., Mills, K., Heterocyclic Chemistry. Blackwel Science, Oxford, 2000.