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Synthesis and study of new phenolic antioxidants with nitroaromatic and heterocyclic substituents
Authors:Email author" target="_blank">O?V?MikhalevEmail author  D?B?Shpakovsky  Yu?A?Gracheva  T?A?Antonenko  D?V?Albov  L?A?Aslanov  E?R?Milaeva
Institution:1.M. V. Lomonosov Moscow State University,Moscow, Russian Federation,Russia
Abstract:New polyfunctional aromatic, nitroaromatic, and heterocyclic compounds linked to the 2,6-di-tert-butylphenol moiety via –NH–, –C(O)NH–, –S–, or–C=N– spacers were synthesized. These structures provide intramolecular charge transfer (ICT) and exhibit antioxidant activity. The structures of the new compounds were established by X-ray diffraction. The novel compounds were evaluated for antioxidant activity using the DPPH assay. The presence of the 2,4,6-trinitrophenyl moiety in combination with the –NH– spacer leads to a considerable increase in the antioxidant activity of 2,6-di-tert-butylphenols. These compounds are also weak lipoxygenase inhibitors. The results of this study provide an opportunity to search for new types of antioxidants with ICT.
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