Document Type
Article
Journal/Book Title
Journal of Chemical Physics
Publication Date
2002
Volume
116
First Page
3635
Last Page
3645
Abstract
The electronic structure and bonding in a series of unligated and ligated FeII porphyrins (FeP) are investigated by density functional theory (DFT). All the unligated four-coordinate iron porphyrins have a 3A2g ground state that arises from the (dxy)2(dz2)2(dπ)2 configuration. The calculations confirm experimental results on Fe tetraphenylporphine but do not support the resonance Raman assignment of Fe octaethylporphine as 3Eg, nor the early assignment of Fe octamethyltetrabenzporphine as 5B2g. For the six-coordinate Fe–P(L)2 (L = HCN, pyridine, CO), the strong-field axial ligands raise the energy of the Fe dz2 orbital, thereby making the iron porphyrin diamagnetic. The calculated redox properties of Fe–P(L)2 are in agreement with experiment. As models for deoxyheme, the energetics of all possible low-lying states of FeP(pyridine) and FeP(2-methylimidazole) have been studied in detail. The groundstate configuration of FeP(2-methylimidazole) was confirmed to be high-spin (dxy)2(dz2)1(dπ)2(dx2−y2)1; FeP (pyridine) is shown to be a poor model for high-spin deoxyheme. © 2002 American Institute of Physics.
Recommended Citation
Electronic structure and bonding in unligated and ligated Fe[sup II] porphyrins Meng-Sheng Liao and Steve Scheiner, J. Chem. Phys. 116, 3635 (2002), DOI:10.1063/1.1447902
Comments
Originally published by American Institute of Physics in the Journal of Chemical Physics.
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