Abstract
AbstractComplexes of iron in high oxidation states are captivating research subjects due to their pivotal role as active intermediates in numerous catalytic processes. Structural and spectroscopic studies of well-defined model complexes often provide evidence of these intermediates. In addition to the fundamental molecular and electronic structure insights gained by these complexes, their reactivity also affects our understanding of catalytic reaction mechanisms for small molecule and bond-activation chemistry. Here, we report the synthesis, structural and spectroscopic characterization of a stable, octahedral Fe(VI) nitrido complex and an authenticated, unique Fe(VII) species, prepared by one-electron oxidation. The super-oxidized Fe(VII) nitride rearranges to an Fe(V) imide through an intramolecular amination mechanism and ligand exchange, which is characterized spectroscopically and computationally. This enables combined reactivity and stability studies on a single molecular system of a rare high-valent complex redox pair. Quantum chemical calculations complement the spectroscopic parameters and provide evidence for a diamagnetic (S = 0) d2 Fe(VI) and a genuine S = 1/2, d1 Fe(VII) configuration of these super-oxidized nitrido complexes.
Funder
Bundesministerium für Bildung und Forschung
Erlangen National High-Performance Computing Center NHR@FAU n100af10
Alexander von Humboldt-Stiftung
Deutsche Forschungsgemeinschaft
Max-Planck-Gesellschaft
European Synchrotron Radiation Facility
U.S. Department of Energy
Publisher
Springer Science and Business Media LLC
Cited by
6 articles.
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