DFT study of radical mechanism for the reaction of dihydroxifumaric acid with the stable radical DPPH<sup>•</sup>.

Автор(и)

  • I. Arsene Institute of Chemistry Tiraspol State University
  • M. Yu. Gorbachev Institute of Chemistry
  • N. N. Gorinchoy Institute of Chemistry

Анотація

Many organic compounds with enol or phenol groups are effective antioxidants which transform various free radicals into their diamagnetic derivatives [1]. From the literature it is known that dihydroxyfumaric acid (DHFA) is a very powerful antioxidant [2], having inhibitory properties pronounced against free radicals. In the work [3] we have proposed and studied the ionic mechanism describing interaction between dihydroxyfumaric acid (DHFA) and the stable radical DPPH.

Посилання

W. Brand-Williams, M.E. Cuvelier, C. Berset, Food Science and Technology, 1995, 28, 25–30.

N. Secara, Gh. Duca, L. Vlad, F. Macaev, Chem. J. Mold. 2010, 5 (2), 59–67

M. Gorbachev, N. Gorinchoy, I. Arsene, Chem. J. Mold. 2015, 10(1), 89–94.

D.N. Laikov, PRIRODA, Electronic Structure Code, Version 6, 2006.

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Номер

2020

Розділ

Квантова хімія