Résumé
New non-symmetrical, redox-active imino NHC pyridine pincer ligands, 2-(R1-imidazol-2-ylidene)-6-(R2NCH)-pyridine (R1 = 2,6-diisopropylphenyl (DiPP), R2 = 2,4,6-trimethylphenyl (Mes), 4B; R1 = R2 = DiPP, 4C), have been accessed by a ZnII-promoted modular synthesis involving the quaternization of R1-imidazole by [Zn(κNimineκNpyridine)(2-(R2NCH)-6-bromo-pyridine)Cl2], followed by ZnII removal and deprotonation of imidazolium pro-ligands. Redox active forms of 4B were implicated in the two complexes obtained by its reaction with FeBr2/KC8; metrical data analysis pointed to the occurrence of radical anionic and dianionic redox states of 4B.
| langue originale | Anglais |
|---|---|
| Pages (de - à) | 5955-5964 |
| Nombre de pages | 10 |
| journal | Dalton Transactions |
| Volume | 46 |
| Numéro de publication | 18 |
| Les DOIs | |
| état | Publié - 1 janv. 2017 |
| Modification externe | Oui |
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