Models of High-Valent Heme Protein Intermediates:  A Quantum Chemical Study of Iron(IV) Porphyrins with Two Univalent Axial π-Bonding Ligands Jeanet Conradie Jannie C. Swarts Abhik Ghosh 10.1021/jp030817p.s001 https://acs.figshare.com/articles/journal_contribution/Models_of_High_Valent_Heme_Protein_Intermediates_A_Quantum_Chemical_Study_of_Iron_IV_Porphyrins_with_Two_Univalent_Axial_Bonding_Ligands/3353989 This is a quantum chemical survey of a broad class of high-valent transition metal intermediates relevant to the catalytic cycles of the cytochromes P<sub>450</sub> and related heme proteins, viz. iron(IV) and manganese(IV) porphyrins with two univalent π-bonding axial ligands. The axial ligands in these intermediates invariably exhibit a bent geometry, reflecting a competitive interplay of σ- and π-bonding effects. Compared to an oxo ligand, the univalent ligands are distinctly less able to delocalize electronic spin density away from the metal center, which might have significant implications for the chemical reactivity of these species. 2004-01-08 00:00:00 Quantum Chemical Study quantum chemical survey intermediate chemical reactivity oxo ligand cytochromes P 450 heme proteins metal center