Influence of a "Dangling" Co(II) Ion Bound to a [MnCo3O4] Oxo Cubane.
Andy I NguyenLucy E DaragoDavid BalcellsT Don TilleyPublished in: Journal of the American Chemical Society (2018)
Cobalt(II), in the presence of acetate and nitrate, quantitatively adds to the manganese-cobalt oxido cubane MnIVCoIII3O4(OAc)5(py)3 (1) to furnish the pentametallic dangler complex MnIVCoIII3CoIIO4(OAc)6(NO3)(py)3 (2). Complex 2 is structurally reminiscent of photosystem II's oxygen-evolving center, and is a rare example of a transition-metal "dangler" complex. Superconducting quantum interference device magnetometry and density functional theory calculations characterize 2 as having an S = 0 ground state arising from antiferromagnetic coupling between the CoII and MnIV ions. At higher temperatures, an uncoupled state dominates. The voltammogram of 2 has four electrochemical events, two more than that of its parent cubane 1, suggesting that addition of the dangler increases available redox states. Structural, electrochemical, and magnetic comparisons of complexes 1 and 2 allow a better understanding of the dangler's influence on a cubane.
Keyphrases
- density functional theory
- molecular dynamics
- molecularly imprinted
- transition metal
- electron transfer
- gold nanoparticles
- ionic liquid
- nitric oxide
- reduced graphene oxide
- energy transfer
- drinking water
- quantum dots
- carbon nanotubes
- molecular dynamics simulations
- monte carlo
- aqueous solution
- solid phase extraction
- metal organic framework
- simultaneous determination