Molecular-level insights into intrinsic peroxidase-like activity of nanocarbon oxides

Chemistry. 2015 Jan 12;21(3):960-4. doi: 10.1002/chem.201404647. Epub 2014 Nov 20.

Abstract

Nanocarbon oxides have been proved to possess great peroxidase-like activity, catalyzing the oxidation of many peroxidase substrates, such as 3,3',5,5'-tetramethylbenzidine (TMB) and o-phenylenediamine dihydrochloride (OPD), accompanied by a significant color change. This chromogenic reaction is widely used to detect glucose and occult blood. The chromogenic reaction was intensively investigated with density functional theory and molecular-level insights into the nature of peroxidase-like activity were gained. A radical mechanism was unraveled and the carboxyl groups of nanocarbon oxides were identified as the reactive sites. Aromatic domains connected with the carboxyl groups were critical to the peroxidase-like activity.

Keywords: carboxyl; density functional calculations; nanocarbon oxides; peroxidase; reaction mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzidines / chemistry
  • Benzidines / metabolism
  • Catalysis
  • Hydrogen Peroxide / chemistry
  • Nanotubes, Carbon / chemistry*
  • Oxidation-Reduction
  • Oxides / chemistry*
  • Peroxidase / chemistry
  • Peroxidase / metabolism
  • Phenylenediamines / chemistry
  • Phenylenediamines / metabolism
  • Thermodynamics

Substances

  • Benzidines
  • Nanotubes, Carbon
  • Oxides
  • Phenylenediamines
  • 3,3',5,5'-tetramethylbenzidine
  • Hydrogen Peroxide
  • Peroxidase