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Fractional transfer of a free unpaired electron to overcome energy barriers in the formation of Fe4+ from Fe3+ during the core contraction of macrocycles: implication for heme distortion
- Source :
- Organic & Biomolecular Chemistry. 13:2939-2946
- Publication Year :
- 2015
- Publisher :
- Royal Society of Chemistry (RSC), 2015.
-
Abstract
- The free unpaired electron in Fe(3+) ions cannot be directly removed, and needs a transfer pathway with at least four steps to overcome the high energy barriers to form Fe(4+) ions. Fine changes in the electronic structure of Fe(3+) ions on spin conversion were identified through a deeper analysis of the diffraction, spectral and electrochemical data for six non-planar iron porphyrins. Fe(3+) ions can form four d electron tautomers as the compression of the central ion is increased. This indicates that the Fe(3+) ion undergoes a multistep electron transfer where the total energy gap of electron transfer is split into several smaller gaps to form high-valent Fe(4+) ions. We find that the interchange of these four electron tautomers is clearly related to the core size of the macrocycle in the current series. The large energy barrier to produce iron(iv) complexes is overcome through a gradient effect of multiple energy levels. In addition, a possible porphyrin Fe(3+)˙ radical may be formed from its stable isoelectronic form, porphyrin Fe(3+), under strong core contraction. These results indicate the important role of heme distortion in its catalytic oxidation functions.
- Subjects :
- Models, Molecular
Porphyrins
Free Radicals
Iron
Molecular Conformation
Electrons
Heme
Electron
Electronic structure
Crystallography, X-Ray
Electrochemistry
Biochemistry
Catalysis
Ion
chemistry.chemical_compound
Electron transfer
Molecule
Physical and Theoretical Chemistry
Ions
Molecular Structure
Chemistry
Organic Chemistry
Electron Spin Resonance Spectroscopy
Cobalt
Porphyrin
Oxygen
Crystallography
Unpaired electron
Atomic physics
Oxidation-Reduction
Subjects
Details
- ISSN :
- 14770539 and 14770520
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- Organic & Biomolecular Chemistry
- Accession number :
- edsair.doi.dedup.....277b87be6e2bc2f63957947b8a791aab
- Full Text :
- https://doi.org/10.1039/c4ob02429j