Keilwerth Martin, Mao Weiqing, Malischewski Moritz, Jannuzzi Sergio A V, Breitwieser Kevin, Heinemann Frank W, Scheurer Andreas, DeBeer Serena, Munz Dominik, Bill Eckhard, Meyer Karsten
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Department of Chemistry and Pharmacy, Inorganic Chemistry, Erlangen, Germany.
Freie Universität Berlin, Institute of Chemistry and Biochemistry, Inorganic Chemistry, Berlin, Germany.
Nat Chem. 2024 Apr;16(4):514-520. doi: 10.1038/s41557-023-01418-4. Epub 2024 Jan 30.
Complexes 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) d Fe(VI) and a genuine S = 1/2, d Fe(VII) configuration of these super-oxidized nitrido complexes.
高氧化态铁的配合物是引人入胜的研究对象,因为它们在众多催化过程中作为活性中间体发挥着关键作用。对明确的模型配合物进行结构和光谱研究常常能为这些中间体提供证据。除了通过这些配合物获得的基本分子和电子结构见解外,它们的反应性也影响着我们对小分子和键活化化学催化反应机制的理解。在此,我们报告了一种稳定的八面体Fe(VI)氮化物配合物以及一种经鉴定的独特Fe(VII)物种的合成、结构和光谱表征,它们是通过单电子氧化制备的。超氧化的Fe(VII)氮化物通过分子内胺化机制和配体交换重排为Fe(V)亚胺,这一过程通过光谱和计算进行了表征。这使得能够对一个罕见的高价配合物氧化还原对的单一分子体系进行反应性和稳定性的联合研究。量子化学计算补充了光谱参数,并为这些超氧化氮化物配合物的抗磁性(S = 0)d Fe(VI)和真正的S = 1/2、d Fe(VII)构型提供了证据。