Catechol oxidase activity of comparable dimanganese and dicopper complexes

Dalton Trans. 2018 Nov 21;47(43):15555-15564. doi: 10.1039/c8dt01378k. Epub 2018 Oct 22.

Abstract

Synthetic Cu complexes have been widely investigated as model systems for catechol oxidase enzymes. The catechol oxidase reactivity of Mn complexes has been less explored, and the effect of metal substitution in catecholase mimics has not been explored. A series of Mn and Cu complexes supported by the same poly-benzimidazole ligand framework have been synthesised and investigated in catecholase activity in acetonitrile medium using 3,5-di-tert-butylcatechol (3,5-DTBC) as a substrate. The Cu complexes proved to be good catechol oxidase mimics with moderate kcat values (∼45 h-1). The kinetic parameters for Mn complexes exhibited lower kcat values (∼8-40 h-1) when compared to the Cu complexes. Our findings demonstrate that later transition metals supported by relatively electron rich ligands yield the highest kcat values for catechol oxidation.

MeSH terms

  • Biomimetic Materials / chemical synthesis
  • Biomimetic Materials / chemistry*
  • Catechol Oxidase / metabolism*
  • Catechols / chemistry
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / chemistry*
  • Copper / chemistry*
  • Manganese / chemistry*
  • Models, Molecular
  • Molecular Conformation
  • Oxidation-Reduction

Substances

  • Catechols
  • Coordination Complexes
  • Manganese
  • Copper
  • Catechol Oxidase
  • catechol