CaMn₃^(IV)O₄ Cubane Models of the Oxygen Evolving Complex: Spin Ground States S < 9/2 and the Effect of Oxo Protonation

Abstract

We report the single crystal XRD and MicroED structure, magnetic susceptibility, and EPR data of a series of CaMn₃^(IV)O₄ and YMn₃^(IV)O₄ complexes as structural and spectroscopic models of the cuboidal subunit of the oxygen-evolving complex (OEC). The effect of changes in heterometal identity, cluster geometry, and bridging oxo protonation on the spin-state structure was investigated. In contrast to previous computational models, we show that the spin ground state of CaMn₃^(IV)O₄ complexes and variants with protonated oxo moieties need not be S = 9/2. Desymmetrization of the pseudo-C₃-symmetric Ca(Y)Mn₃^(IV)O₄ core leads to a lower S = 5/2 spin ground state. The magnitude of the magnetic exchange coupling is attenuated upon oxo protonation, and an S = 3/2 spin ground state is observed in CaMn₃^(IV)O₃(OH). Our studies complement the observation that the interconversion between the low-spin and high-spin forms of the S₂ state is pH-dependent, suggesting that the (de)protonation of bridging or terminal oxygen atoms in the OEC may be connected to spin-state changes.

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