Abstract
The coordination chemistry of calix[4]azacrowns obtained from the reaction of a diester calix[4]arene with diethylenetriamine provided unusual copper(II) and manganese(II) complexes in which calix[4]azacrown acts as a bidentate N,O-donor ligand, in some cases, but as a unidentate N-donor ligand, in other cases. The first example of a binuclear ruthenium(II)/manganese(II) complex, involving the calix[4]arene framework as the bridging ligand, is also reported. The calix[4]arene framework consists of a bipyridyl unit connected at the upper rim of the calix[4]arene, through an amide linkage, and an azacrown unit at the lower rim, also connected through amide groups.
| Original language | English |
|---|---|
| Pages (from-to) | 749-756 |
| Number of pages | 8 |
| Journal | European Journal of Inorganic Chemistry |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 2007 |
Keywords
- Calix[4]arene
- Copper(II)
- EPR spectroscopy
- Heterometallic compounds
- Macrocyclic ligands
- Manganese(II)
- Ruthenium(II)
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