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Updated: Jun 25, 2026
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Published on: December 16, 2013
Energetics and structural consequences of axial ligand coordination in nonplanar nickel porphyrins
Yujiang Song1, Raid E Haddad, Song-Ling Jia
1Biomolecular Materials and Interfaces Department, Sandia National Laboratories, Albuquerque, New Mexico 87185, USA.
Abstract:
The effects of ruffling on the axial ligation properties of a series of nickel(II) tetra(alkyl)porphyrins have been investigated with UV-visible absorption spectroscopy, resonance Raman spectroscopy, X-ray crystallography, classical molecular mechanics calculations, and normal-coordinate structural decomposition analysis. For the modestly nonplanar porphyrins, porphyrin ruffling is found to cause a decrease in binding affinity for pyrrolidine and piperidine, mainly caused by a decrease in the binding constant for addition of the first axial ligand; ligand binding is completely inhibited for the more nonplanar porphyrins. The lowered affinity, resulting from the large energies required to expand the core and flatten the porphyrin to accommodate the large high-spin nickel(II) ion, has implications for nickel porphyrin-based molecular devices and the function of heme proteins and methyl-coenzyme M reductase.
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