Calculations of One-Electron Redox Potentials of Oxoiron(IV) Porphyrin Complexes

Ludovic Castro, Michael Buehl*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

43 Citations (Scopus)
4 Downloads (Pure)

Abstract

Density functional theory calculations have been performed to calculate the one-electron redox potential for a series of oxoiron(IV) porphyrin complexes of the form [(TMP)Fe-IV(O)(L)] (TMP = 5,10,15,20-tetramesitylporphyrinate). Different axial ligands were chosen (L = none, Im, ClO4-, CH3CO2-, Cl-, F-, SCH3-) in order to compare the results with recent electrochemical experiments. The redox potentials were calculated with a Born-Haber cycle and the use of an internal reference, i.e. the absolute redox potential of ferrocene. Diverse methodologies were tested and show that the computed redox potentials depend strongly on the functional, the basis set, and the continuum models used to compute the solvation energies. Globally, BP86 gives better results for the geometries of the complexes than B3LYP and M06-L as well as more consistent values for the redox potentials. Although the results fit the experimental data for L = Im and L = ClO4-, the addition of the other anionic axial ligands to the oxoiron(IV) porphyrin complex strongly lowers the redox potential, which is in disagreement with experimental observations. This important discrepancy is discussed.

Original languageEnglish
Pages (from-to)243-251
Number of pages9
JournalJournal of Chemical Theory and Computation
Volume10
Issue number1
Early online date20 Nov 2013
DOIs
Publication statusPublished - Jan 2014

Keywords

  • Solvation free energies
  • Cation radical complexes
  • Continuum dielectric theory
  • Transition metal complexes
  • Density functional theory
  • Axial ligand
  • CYTOCHROME-P450 ENZYMES
  • Compound I
  • Horseradish peroxidase
  • Computational electrochemistry

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