Abstract

The N,N′-coordinated mononuclear complex Eu(TTA)3(pdn), prepared by treating 1,10-phenanthroline-5,6-dione (pdn) with Eu(TTA)3(H2O)2 (HTTA = 2-thenoyltrifluoroacetone), may be used as a benzoquinone-like ligand through the oxygen donor atoms in reaction with an additional Eu(TTA)3(H2O)2 precursor to give the dinuclear complex Eu2(TTA)6(pdn). Both the mono- and dinuclear complexes were characterized by elemental analysis, IR, TG, MS, and 1H NMR spectra. The results indicated that they both exhibited a characteristic red emission peak at 616 nm, corresponding to the 5D0 → 7F2 transition of Eu(III) ions under UV excitation. Compared with the mononuclear complex, the dinuclear complex presented better thermal stability and stronger luminescence, which makes it a promising light-conversion molecular device. .

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