Standard Redox Potentials of Fe(III) Aqua Complexes Included into the Cavities of Cucurbit[ n]urils ( n = 6-8): A DFT...

An approach for estimating at the DFT level of the standard redox potentials of the inclusion compounds based on Fe(III) and Fe(II) aqua complexes inside the cavities of cucurbit[ n]urils ( n = 6-8) has been proposed. These inclusion compounds were established to have compositions which can be described by the formulas [Fe(H₂O)₆]^3+/2+@CB[6] and [Fe(H₂O)₆·4H₂O]^3+/2+@CB[7,8]. Redox potentials E⁰ relative to the standard hydrogen electrode for the half-reaction Fe(III)/Fe(II) in the CB[ n] cavities calculated at the PBE/TZVP level within the molecular-continuum solvation model are 1.607, 0.949, and 0.847 V for n = 6, 7, and 8, respectively. The obtained values indicate a relative increase of the oxidative ability of Fe(III) aqua-ions in the cavities of the examined CB[ n], especially in CB[6], compared to the calculated value ( E⁰ = 0.786 V) for the same half-reaction in the bulk of aqueous solution. Possible causes of the detected trend are discussed. The calculations also showed that the Fe(III) aqua complex inside the CB[6] changes its magnetic properties, transforming into a low-spin state with a total spin S = 1/2, whereas for all other systems high-spin states in accord with the classical ligand field theory are realized.