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The adsorption of dibenzyl disulfide (DBDS) on a pentagonal bipyramid Cu7 cluster was investigated by using density functional calculations, from energetic and electronic viewpoints. The resulting complexes are mainly driven by Cu···S interaction, and an extra stabilization can be conferred by a secondary π···Cu weak interaction. They were classified as physi- or chemisorption according to their binding energy, and by applying a distortion/interaction decomposition model. Disulfide bond dissociation was observed in the most stable complexes, which includes higher distortion energy. From an electronic viewpoint, an electronic flow from copper to DBDS was observed. [ABSTRACT FROM AUTHOR]

Hydroxyl radical reduction and peroxide bond breaking in hydrogen peroxide are reactions involved in various processes such as the Fenton reaction, which has applications as e.g. groundwater remediation. Here, we study these two reactions from a thermodynamical point of view through the bond dissociation energy (BDE) of the O-O bond in hydrogen peroxide and the electron affinity (EA) of the hydroxyl radical. High-level ab-initio calculations at the complete basis set (CBS) limit were carried out, and the performance of different DFT-based methods was addressed by following a specific classification on the basis of the Jacob’s ladder in combination with various Pople’s basis sets. The ab-initio calculations at the CBS limit are in agreement with experimental reference data and identify a significant contribution of the electron correlation energy to the BDE and EA. The studied DFT-based methods were able to reproduce the ab-initio reference values, although no functional was particularly detected as the best for both reactions. The inclusion of certain percentage of Hartree-Fock (HF) exchange in DFT functionals leads in most cases to smaller BDE and EA values, which might be related to the poor description of the two reactions by the HF method. Considering the computational cost, DFT methods provide better BDE and EA values than HF methods with an accuracy comparable to the MP2 or CCSD level of theory. Additionally, the quality of the hydrogen peroxide, hydroxyl radical and hydroxyl anion structures obtained from these functionals was compared to experimental reference data. In general, bond lengths were well reproduced and the errors in the angles were between one and two degrees with some systematic trend with respect to the basis set’s size. From our results we conclude that DFT methods present a computationally less expensive alternative to describe these two reactions that play a role in the Fenton reaction. The benchmark that is carried out in this study provides a systematic validation of various approximated Exc[ρ] functionals combined with different basis sets, which could serve as a stepping-stone for future research on the Fenton reaction. [ABSTRACT FROM AUTHOR]