| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1340252 | Polyhedron | 2009 | 5 Pages |
Two hexanuclear zinc(II) complexes, [Zn6(L1)2(μ2-OH)2(μ2-CH3COO)8] · CH3CN (1 · CH3CN) and [Zn6(L2)2(μ2-OH)2(μ2-CH3COO)8] · 4CH3CN (2 · 4CH3CN), where HL1 = 4-methyl-2,6-bis(cyclohexylmethyliminomethyl)-phenol and HL2 = 4-methyl-2,6-bis(1-naphthalylmethyliminomethyl)-phenol, have been synthesized and characterized by elemental analysis, FT-IR and fluorescence spectroscopic methods, and by X-ray diffraction analysis. In the asymmetric unit of complex 1, two of the three zinc atoms have pentacoordinate geometries and the other is tetrahedrally coordinated, whereas the three distinct Zn atoms in complex 2 adopt three different coordination environments, namely distorted octahedral, trigonal bipyramidal and tetrahedral. The fluorescence properties of the ligands and complexes have been investigated.
Graphical abstractTwo Schiff-base ligands, 4-methyl-2,6-bis(cyclohexanemethyliminomethyl)-phenol and 4-methyl-2,6-bis(1-naphthalenemethyliminomethyl)-phenol, have been synthesized and characterized. Two hexanuclear zinc(II) complexes with these N2O donor ligand have also been synthesized and characterized by X-ray diffraction analysis. Fluorescence property studies of the ligands and their complexes reveal that the quantum yields increase upon complexation.Figure optionsDownload full-size imageDownload as PowerPoint slide
