4.6 Article

Toluene nitration in irradiated nitric acid and nitrite solutions

Journal

RADIATION PHYSICS AND CHEMISTRY
Volume 80, Issue 4, Pages 554-560

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.radphyschem.2010.12.005

Keywords

Toluene radiolysis; HPLC; UV spectra; LC-MS; Free-radicals; Electrophilic substitution

Funding

  1. U.S. Department of Energy (DOE), Office of Nuclear Energy, Science and Technology [DEAC07-99ID13727]
  2. Office of Basic Energy Sciences, U.S. Department of Energy

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The kinetics, mechanisms, and stable products produced for the nitration of aryl alkyl mild ortho-para director toluene in irradiated nitric acid and neutral nitrite solutions were investigated using gamma and pulse radiolysis. Electron pulse radiolysis was used to determine the bimolecular rate constants for the reaction of toluene with different transient species produced by irradiation. HPLC with UV detection, GC-MS and LC-MS, were used to assess the stable reaction products. Free-radical based nitration reaction products were found in irradiated acidic and neutral media. In 6.0 M HNO(3), ring substitution, side chain substitution, and oxidation, produced different nitrated toluene products. For ring substitution, nitrogen oxide radicals were added mainly to cyclohexadienyl radicals, whereas for side chain substitution, these radicals were added to the carbon-centered benzyl radical produced by H-atom abstraction. In neutral nitrite solutions, radiolytically-induced ring nitration products approached a statistically random distribution, suggesting a direct free-radical reaction involving addition of the (center dot)NO(2) radical. (C) 2010 Elsevier Ltd. All rights reserved.

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