Abstract
The ligand 2,7-bis(6-methyl-2-pyridyl)-1,8-naphthyridine (MeL) acts as a dinucleating analogue of ubiquitous 2,2′-bipyridine ligands. Coordination of MeL to [Cu(NCMe)4]PF6 and Zn(OAc)2 led to isolation of monometallic [Zn(OAc)2(MeL)], homobimetallic [Cu2(MeL)2][PF6]2, and heterobimetallic [CuZn(μ-OAc)2(MeL)]PF6 complexes. The redox-active nature of the ligand enables access to four redox states of the complex [Cu2(MeL)2][PF6]2. DFT studies indicate that these comprise a metal-centered oxidative and ligand-centered reductive processes.
| Original language | English |
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| Pages (from-to) | 19333-19343 |
| Number of pages | 11 |
| Journal | Inorganic Chemistry |
| Volume | 61 |
| Issue number | 48 |
| DOIs | |
| Publication status | Published - 5 Dec 2022 |