Are the reduction and oxidation properties of nitrocompounds dissolved in water different from those produced when
Liudmyla K Sviatenko1, Olexandr Isayev, Leonid Gorb
1Department of Chemistry and Biochemistry, Interdisciplinary Nanotoxicity Center, Jackson State University, Jackson, Mississippi, 39217; Department of Organic Chemistry, Oles Honchar Dnipropetrovsk National University, Dnipropetrovsk, 49010, Ukraine.
Abstract:
The reduction and oxidation properties of four nitrocompounds (trinitrotoluene [TNT], 2,4-dinitrotoluene, 2,4-dinitroanisole, and 5-nitro-2,4-dihydro-3H-1,2,4-triazol-3-one [NTO]) dissolved in water as compared with the same properties for compounds adsorbed on a silica surface were studied. To consider the influence of adsorption, cluster models were developed at the M05/tzvp level. A hydroxylated silica (001) surface was chosen to represent a key component of soil. The PCM(Pauling) and SMD solvation models were used to model water bulk influence. The following properties were analyzed: electron affinity, ionization potential, reduction Gibbs free energy, oxidation Gibbs free energy, and reduction and oxidation potentials. It was found that adsorption and solvation decrease gas phase electron affinity, ionization potential, and Gibbs free energy of reduction and oxidation, and thus, promote redox transformation of nitrocompounds. However, in case of solvation, the changes are more significant than for adsorption. This means that nitrocompounds dissolved in water are easier to transform by reduction or oxidation than adsorbed ones. Among the considered compounds, TNT was found to be the most reactive in an electron attachment process and the least reactive for an electron detachment transformation. During ionization, a deprotonation of adsorbed NTO was found to occur.
More Related Videos
Related Concept Videos
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Oxidation and Reduction of Organic Molecules
The removal of an electron from a molecule, results in a...
Redox Titration: Other Oxidizing and Reducing Agents
2° Amines to N-Nitrosamines: Reaction with NaNO2
Reactions at the Benzylic Position: Oxidation and Reduction
Balancing Redox Equations


