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Theoretical Insights into the Reaction Mechanism between 2,3,7,8-Tetrachlorodibenzofuran and Hydrogen Peroxide: A DFT Study

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journal contribution
posted on 07.01.2019, 09:17 by Nana Bai, Weihua Wang, Yun Zhao, Wenling Feng, Ping Li
A detailed knowledge of the reactivity of 2,3,7,8-tetrachlorodibenzofuran (TCDF) at the molecular level is important to better understand the transformation of dioxins analogous to TCDF in the environment. To clarify the reactivity of the organic hydroperoxides toward TCDF, the reaction of the TCDF with hydrogen peroxide (H2O2) and its anion has been investigated theoretically. For the reaction of the neutral H2O2, a molecular complex can be formed between TCDF and H2O2 first. Then, the nucleophilic aromatic substitution of TCDF by H2O2 occurs in the presence of the water molecules to form an intermediate containing an O–O bond. Finally, the O–O bond cleavages homolytically for the above intermediate. On the other hand, as for the reaction of the anion of H2O2 (HO2), the nucleophilic addition of HO2 to TCDF can also occur besides the nucleophilic aromatic substitution reaction mentioned above, resulting in the dissociation of the C–O bond of TCDF. Unlike the reaction involving neutral H2O2, no water molecules are required. In addition, the selected substitution effects, such as F-, Br-, and CH3-substituents, on the reactivity of the above reaction have also been explored. Hopefully, the present results can enable us to gain insights into the reactivity of the organic hydroperoxides with TCDF-like environmental pollutants.

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