Abstract
Successive chemical reductions of the heteroleptic complex [(tpy)Cr III(tphz)] 3+(tpy = terpyridine; tphz = tetrapyridophenazine) give rise to the mono- and di-radical redox isomers, [(tpy)Cr III(tphz? -)] 2+and [(tpy? -)Cr III(tphz? -)] +, respectively. As designed, the optimized overlap of the involved magnetic orbitals leads to extremely strong magnetic interactions between theS= 3/2 metal ion andS= 1/2 radical spins, affording well isolatedS T= 1 andS T= 1/2 ground states at room temperature.
| Original language | English |
|---|---|
| Pages (from-to) | 4906-4909 |
| Number of pages | 4 |
| Journal | Chemical Communications |
| Volume | 56 |
| Issue number | 36 |
| Early online date | 24 Mar 2020 |
| DOIs | |
| Publication status | Published - 4 May 2020 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- General Chemistry
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry