Fine tuning of the redox-active diguanidine ligand in cationic cobalt complexes for electronic structure control

In this work we show that the redox chemistry of hexacoordinated cobalt complexes with redox-active diguanidine ligands could be tuned by modifying the diguanidine and/or the co-ligands. In this way, one-electron oxidation could be directed to be either ligand- or metal-centered, leading to high-spi...

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Hauptverfasser: Osterbrink, Johanna (VerfasserIn) , Kaliske, Meret (VerfasserIn) , Schulz, Maximilian (VerfasserIn) , Koepcke, Hanna (VerfasserIn) , Hübner, Olaf (VerfasserIn) , Kaifer, Elisabeth (VerfasserIn) , Himmel, Hans-Jörg (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 2, 2025
In: Chemistry - a European journal
Year: 2025, Jahrgang: 31, Heft: 51, Pages: 1-15
ISSN:1521-3765
DOI:10.1002/chem.202501382
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/chem.202501382
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202501382
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Verfasserangaben:Johanna Osterbrink, Meret Kaliske, Maximilian Schulz, Hanna Koepcke, Olaf Hübner, Elisabeth Kaifer, and Hans-Jörg Himmel
Beschreibung
Zusammenfassung:In this work we show that the redox chemistry of hexacoordinated cobalt complexes with redox-active diguanidine ligands could be tuned by modifying the diguanidine and/or the co-ligands. In this way, one-electron oxidation could be directed to be either ligand- or metal-centered, leading to high-spin CoII complexes with an oxidized, radical-monocationic diguanidine ligand (ligand-centered oxidation) or low-spin CoIII complexes with a reduced, neutral diguanidine ligand. Further fine-tuning of the redox-active diguanidine ligand leads to a harmonization of the energies of both redox isomers. Consequently, ligand- as well as metal-centered one-electron oxidation is observed, resulting in a mixture of both redox isomers. Quantum-chemical calculations confirm the energetic proximity of the two redox isomers in this bistable system. The results of this work contribute to the development of a directed approach toward the design of bistable cobalt-guanidine complexes and their possible applications in spin-switching devices.
Beschreibung:Gesehen am 24.11.2025
Beschreibung:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.202501382