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Resonance Raman study of oxoiron(IV) porphyrin π-cation radical complex: Porphyrin ligand effect on ν(Fe=O) frequency.
- Source :
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Journal of Inorganic Biochemistry . Jun2024, Vol. 255, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
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Abstract
- Resonance Raman (rR) spectroscopy has been applied to study the nature of the iron-oxo (Fe=O) moiety of oxoiron(IV) porphyrin π-cation radical complex (CompI). While the axial ligand effect on the nature of the Fe=O moiety has been studied with rR spectroscopy, the porphyrin ligand effect has not been studied well. Here, we investigated the porphyrin ligand effect on the Fe=O moiety with rR spectroscopy. The porphyrin ligand effect was modulated by the electron-withdrawing effect of the porphyrin substituent at the meso-position. This study shows that the frequency of the Fe=O stretching band, ν (Fe=O), hardly change even when the electron-withdrawing effect of the porphyrin substituent changes. This result is further supported by theoretical calculation of CompI. The natural atomic charge analysis reveals that the oxo and axial ligands work to buffer the electron-withdrawing effect of the porphyrin substituent. The electron-withdrawing porphyrin substituent shifts an electron population from the ferryl iron to the porphyrin, but the decreased electron population on the ferryl iron is compensated by the shift of the electron population from the oxo ligand and the axial ligand. The shift of the electron population makes the Fe–axial ligand bond length short, but the Fe=O bond length unchanged, resulting in the invariable ν (Fe=O) frequency. We investigated the electron-withdrawing effect of the porphyrin ligand on the iron-oxo (Fe=O) moiety with resonance Raman spectroscopy. This study shows that the frequency of the Fe=O stretching band hardly change even when the electron-withdrawing effect of the porphyrin substituent changes. [Display omitted] • Electron-withdrawing effect of the porphyrin ligand on the iron-oxo stretching band. • Frequency of the iron-oxo stretching band is insensitive to the porphyrin ligand effect. • The oxo and axial ligands work to buffer the porphyrin ligand effect. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 01620134
- Volume :
- 255
- Database :
- Academic Search Index
- Journal :
- Journal of Inorganic Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 176588886
- Full Text :
- https://doi.org/10.1016/j.jinorgbio.2024.112544