Ab initio calculations explore iron(III) hydration dynamics, revealing detailed molecular interactions.
The energies, structures, and vibrational frequencies of [Fe(H2O)n]3+, n = 0–6, 18 have been calculated at the Hartree–Fock, second-order Møller–Plesset, and density functional (B3LYP) levels of theory using the 6−31G* and 6−31+G* basis sets. The metal–oxygen distances and stretching frequencies were compared with each other, with related crystal structure and solution measurements and with previous calculations. The Fe-O distances and stretching vibrational frequencies were well reproduced with an explicit model for the second hydration shell.
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Pye et al. (2026) studied this question.
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