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A Mesoionic Diselenolene Anion and the Corresponding Radical Dianion
Dichalcogenolenes are archetypal redox non‐innocent ligands with numerous applications. Herein, a diselenolene ligand with fundamentally different electronic properties is described. A mesoionic diselenolene was prepared by selenation of a C2‐protected imidazolium salt. This ligand is diamagnetic, w...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322424/ https://www.ncbi.nlm.nih.gov/pubmed/35388932 http://dx.doi.org/10.1002/chem.202200893 |
Sumario: | Dichalcogenolenes are archetypal redox non‐innocent ligands with numerous applications. Herein, a diselenolene ligand with fundamentally different electronic properties is described. A mesoionic diselenolene was prepared by selenation of a C2‐protected imidazolium salt. This ligand is diamagnetic, which is in contrast to the paramagnetic nature of standard dichalcogenolene monoanions. The new ligand is also redox‐active, as demonstrated by isolation of a stable diselenolene radical dianion. The unique electronic properties of the new ligand give rise to unusual coordination chemistry. Thus, preparation of a hexacoordinate aluminum tris(diselenolene) complex and a Lewis acidic aluminate complex with two ligand‐centered unpaired electrons was achieved. |
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