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Mono- and dinuclear europium(III) complexes with thenoyltrifluoroacetone and 1,10-phenanthroline-5,6-dione

机译:单核和双核euro与壬基三氟丙酮和1,10-菲咯啉-5,6-二酮的配合物

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摘要

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 Eu-2(TTA)(6)(pdn). Both the mono- and dinuclear complexes were characterized by elemental analysis, IR, TG, MS, and H-1 NMR spectra. The results indicated that they both exhibited a characteristic red emission peak at 616 nm, corresponding to the D-5(0) -> F-7(2) 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.
机译:N,N'配位的单核复合物Eu(TTA)(3)(pdn),通过用Eu(TTA)(3)(H2O)(2)处理1,10-菲咯啉-5,6-二酮(pdn)制得)(HTTA = 2-thenoyltrifluoroacetone),可通过氧供体原子与另外的Eu(TTA)(3)(H2O)(2)前体反应,用作苯醌类配体,从而生成双核络合物Eu-2 (TTA)(6)(pdn)。单核和双核复合物均通过元素分析,IR,TG,MS和H-1 NMR光谱进行表征。结果表明,它们都在616 nm处显示了特征性的红色发射峰,对应于UV激发下Eu(III)离子的D-5(0)→F-7(2)跃迁。与单核配合物相比,双核配合物表现出更好的热稳定性和更强的发光性,使其成为有前途的光转换分子器件。

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