Abstract
A new β-diiminate ligand (the bis(1-methyl-4,5-diphenyl-1H-imidazol-2-yl)methane anion, BMIMPh2−) is introduced, in which the ligand framework bears an extended imidazole-based π-system in conjugation with a formal β-diketiminates (NacNac) backbone. Bis-ligated transition metal complexes (Co, Zn) featuring this anionic ligand undergo a series of four consecutive single-electron oxidations that are all ligand-based. The singly and doubly oxidized complexes can be synthesized on a preparative scale and have been fully characterized by various spectroscopic techniques. This is in sharp contrast to the corresponding NacNac-based complexes in which only singly oxidized complexes were isolated and characterized. Single crystal X-ray structure determination revealed a correlation between the intra-ligand metrical parameters and the oxidation state of BMIMPh2−. These structural changes in the ligand framework make BMIMPh2− as a perceptible non-innocent ligand in contrast to NacNac type ligands.
Original language | English |
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Pages (from-to) | 10732-10737 |
Journal | Chemistry - A European Journal |
Volume | 23 |
Issue number | 45 |
DOIs | |
Publication status | Published - 10 Aug 2017 |
Keywords
- bis(alkylimidazole)methane
- cobalt and zinc complexes
- redox noninnocence
- β-diiminate
- π-radical ligand