| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1304927 | Inorganic Chemistry Communications | 2007 | 4 Pages |
A new dicadmium(II) complex [Cd2(L)2(H2O)2](NO3)4 · 8H2O (1) with the tripodal amide ligand L (tris[3-aza-2-oxo-4-(2-pyridyl)butyl]amine) was synthesized and structurally characterized. Complex 1 is revealed as a dinuclear 2:2 (Cd:L) complex, in which each cadmium(II) ion is hepta-coordinated with the coordination surrounding of distorted monocapped octahedral geometry. Two cadmium(II) ions are dibridged by two carbonyl μ-O atoms forming a Cd2(μ-O)2 parallelogram-type moiety. Interestingly, the dinuclear coordination sphere can be seen as resulting from the fusion of two distorted monocapped octahedral [Cd(L)(H2O)]2+ units through sharing one edge originated from the two carbonyl μ-O atoms as a first example. Comparative NMR, IR and FAB-mass data of 1 are also discussed.
Graphical abstractA new dicadmium(II) complex [Cd2(L)2(H2O)2](NO3)4 · 8H2O (1) with the tripodal amide ligand L (tris[3-aza-2-oxo-4-(2-pyridyl)butyl]amine) was synthesized and structurally characterized. Complex 1 is revealed as a dinuclear 2:2 (Cd:L) complex, in which each cadmium(II) ion is hepta-coordinated with the coordination surrounding of distorted monocapped octahedral geometry.Figure optionsDownload full-size imageDownload as PowerPoint slide
