Validation of Density Functional Modeling Protocols on Experimental Bis(μ-oxo)/μ-η2:η2-Peroxo Dicopper Equilibria
Lewin, J. L.; Heppner, D. E.; Cramer, C. J.
J. Biol. Inorg. Chem. 2007, 12, 1221.
The bis(μ-oxo)/μ-η2:η2-peroxo equilibria for seven supported Cu2O2 cores were studied with different hybrid and non-hybrid density functional theory models, namely BLYP, mPWPW, TPSS, TPSSh, B3LYP, mPW1PW, and MPW1K. Supporting ligands AN, MeAN, PYAN, MePY2, (MeO)2MePY2, (Me2N)2MePY2, and TACNiPr3 were chosen based on the availability of experimental data for comparison. Density functionals were examined with respect to their ability accurately to reproduce experimental properties including in particular geometries and relative energies for the bis(μ-oxo) and side-on peroxo forms. While geometries from both hybrid and non-hybrid functionals were in good agreement with experiment, the incorporation of Hartree Fock (HF) exchange in hybrid density functionals was found to have a large, degrading effect on predicted relative isomer energies. Specifically, hybrid functionals predicted the μ-η2:η2-peroxo isomer to be too stable by roughly 5-10 kcal mol-1 for each 10% of HF exchange incorporated into the model. Continuum solvation calculations predict electrostatic effects to favor bis(μ-oxo) isomers by 1-4 kcal mol-1 depending on ligand size, with larger ligands having smaller differential solvation effects. Analysis of computed molecular partition functions suggests that non-zero measured entropies of isomerization are likely to be primarily associated with interactions between molecular solutes and their first solvation shell.
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