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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.
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http://dx.doi.org/10.1038/s41557-023-01418-4 | DOI Listing |
Dalton Trans
September 2025
School of Optoelectronic Materials and Technology, Jianghan University, Wuhan 430056, China.
The reaction of [Os(N)(L)(CN)] (OsN, HL = 2-(2-hydroxy-5-nitrophenyl)-benzoxazole) with a mixture of acetone and 2,4,6-trimethylaniline (MesNH) affords [Os(L)(CN)(L)] (L = -mesityl-2-(mesitylimino)propanimidamide), where L is derived from the combination of an acetone molecule, a nitrido ligand, and two MesNH units. The reaction of OsN with acetone and the less bulky aniline gives [Os(L)(CN)(L)] (L = 1,3-diphenylguanidine) and phenylacetamide, where L is derived from the combination of three anilines, one acetone, and the nitrido ligand; this reaction results in C-C bond cleavage of acetone. C-C bond cleavage of ketone also occurs in the reaction of OsN with 2-butanone and aniline.
View Article and Find Full Text PDFInorg Chem
September 2025
Departamento de Química Orgánica e Inorgánica/IUQOEM, Universidad de Oviedo, Oviedo E-33071, Spain.
Reaction of [MoCp(μ-Cl)(μ-PBu)(NO)] with Na(Hg) in tetrahydrofuran gave a very air-sensitive species formulated as the oxido-nitrido radical [MoCp(N)(μ-O)(μ-PBu)(NO)] according to density functional theory (DFT) calculations, which follows from a fast N-O bond cleavage of a nitrosyl ligand. Reaction of the latter with (NH)PF yielded the diamagnetic cation [MoCp(μ-N)(O)(μ-PBu)(NO)] as a mixture of and isomers, which display bent-bridging nitrido and terminal oxido ligands, isolated as the corresponding BAr' salts (Ar' = 3,5-CH(CF); Mo-Mo = 2.8365(5) and 2.
View Article and Find Full Text PDFJ Am Chem Soc
July 2025
Anorganisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 276, D-69120 Heidelberg, Germany.
A protocol for the arylation of both N atoms in dinitrogen is presented. This protocol relies on the use of tungsten pincer complexes to split N and generate tungsten nitrides, which were shown to undergo nucleophilic aromatic substitution (SAr) reactions with electron-deficient aryl chlorides. Starting from (N), this two-step process was exploited for the preparation of different N-labeled aryl amines.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2025
Department of Chemistry, Yale University, 225 Prospect St., New Haven, Connecticut, USA.
Reactive rhenium(III) nitride complexes could result from filling Re─N π* orbitals, but such complexes lie beyond the "nitrido wall" and are rare due to their instability. Here, we describe a method for bypassing the nitrido wall by incorporating a redox-active isocyanide supporting ligand, which accommodates two electrons as shown by crystallographic, spectroscopic, and computational studies. These electrons can be returned to the metal during its facile reaction with CO to form a cyanate complex, demonstrating the nucleophilic reactivity of the nitride.
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