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Insights into the mechanism of the reaction between tetrachloro-p- benzoquinone and hydrogen peroxide and their implications in the catalytic role of water molecules in producing the hydroxyl radial

Journal Article


Abstract


  • Detailed mechanisms for the formation of hydroxyl or alkoxyl radicals in the reactions between tetrachloro-p-benzoquinone (TCBQ) and organic hydroperoxides are crucial for better understanding the potential carcinogenicity of polyhalogenated quinones. Herein, the mechanism of the reaction between TCBQ and H2O2 has been systematically investigated at the B3LYP/6-311++G** level of theory in the presence of different numbers of water molecules. We report that the whole reaction can easily take place with the assistance of explicit water molecules. Namely, an initial intermediate is formed first. After that, a nucleophilic attack of H2O2 onto TCBQ occurs, which results in the formation of a second intermediate that contains an OOH group. Subsequently, this second intermediate decomposes homolytically through cleavage of the O-O bond to produce a hydroxyl radical. Energy analyses suggest that the nucleophilic attack is the rate-determining step in the whole reaction. The participation of explicit water molecules promotes the reaction significantly, which can be used to explain the experimental phenomena. In addition, the effects of F, Br, and CH3 substituents on this reaction have also been studied. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

UOW Authors


  •   Sun, Qiao (external author)
  •   Zhao, Yan (external author)
  •   Du, Aijun (external author)
  •   Li, Ping (external author)
  •   Wang, Weihua (external author)
  •   Bi, Siwei (external author)
  •   Li, Zhen

Publication Date


  • 2013

Citation


  • Li, P., Wang, W., Sun, Q., Li, Z., Du, A., Bi, S. & Zhao, Y. (2013). Insights into the mechanism of the reaction between tetrachloro-p- benzoquinone and hydrogen peroxide and their implications in the catalytic role of water molecules in producing the hydroxyl radial. ChemPhysChem: a European journal of chemical physics and physical chemistry, 14 (12), 2737-2743.

Scopus Eid


  • 2-s2.0-84882601671

Ro Metadata Url


  • http://ro.uow.edu.au/aiimpapers/857

Has Global Citation Frequency


Number Of Pages


  • 6

Start Page


  • 2737

End Page


  • 2743

Volume


  • 14

Issue


  • 12

Abstract


  • Detailed mechanisms for the formation of hydroxyl or alkoxyl radicals in the reactions between tetrachloro-p-benzoquinone (TCBQ) and organic hydroperoxides are crucial for better understanding the potential carcinogenicity of polyhalogenated quinones. Herein, the mechanism of the reaction between TCBQ and H2O2 has been systematically investigated at the B3LYP/6-311++G** level of theory in the presence of different numbers of water molecules. We report that the whole reaction can easily take place with the assistance of explicit water molecules. Namely, an initial intermediate is formed first. After that, a nucleophilic attack of H2O2 onto TCBQ occurs, which results in the formation of a second intermediate that contains an OOH group. Subsequently, this second intermediate decomposes homolytically through cleavage of the O-O bond to produce a hydroxyl radical. Energy analyses suggest that the nucleophilic attack is the rate-determining step in the whole reaction. The participation of explicit water molecules promotes the reaction significantly, which can be used to explain the experimental phenomena. In addition, the effects of F, Br, and CH3 substituents on this reaction have also been studied. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

UOW Authors


  •   Sun, Qiao (external author)
  •   Zhao, Yan (external author)
  •   Du, Aijun (external author)
  •   Li, Ping (external author)
  •   Wang, Weihua (external author)
  •   Bi, Siwei (external author)
  •   Li, Zhen

Publication Date


  • 2013

Citation


  • Li, P., Wang, W., Sun, Q., Li, Z., Du, A., Bi, S. & Zhao, Y. (2013). Insights into the mechanism of the reaction between tetrachloro-p- benzoquinone and hydrogen peroxide and their implications in the catalytic role of water molecules in producing the hydroxyl radial. ChemPhysChem: a European journal of chemical physics and physical chemistry, 14 (12), 2737-2743.

Scopus Eid


  • 2-s2.0-84882601671

Ro Metadata Url


  • http://ro.uow.edu.au/aiimpapers/857

Has Global Citation Frequency


Number Of Pages


  • 6

Start Page


  • 2737

End Page


  • 2743

Volume


  • 14

Issue


  • 12