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Syntheses, characterization, and luminescence of two lanthanide complexes [Ln_2(acetate)_6(H_2O)_4]·4H_2O (Ln=Tb(1), Sm(2)) 被引量:1

Syntheses, characterization, and luminescence of two lanthanide complexes [Ln_2(acetate)_6(H_2O)_4]·4H_2O (Ln=Tb(1), Sm(2))
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摘要 Two dinuclear compounds [Ln2(acetate)6(H2O)4]-4H2O (Ln=Tb(1), Sm(2)) were obtained by the hydrothermal reaction of Ln2O3 with malonic acid at 150 ℃. Both compounds were characterized by elemental analyses, infrared spectra, and single crystal X-ray diffraction. The results showed that complexes 1 and 2 were isomorphous and crystallize in triclinic space group P 1. The coordination geometry around Ln(Ⅲ) ions in the complexes 1 and 2 was a distorted tricapped trigonal prism with a nine coordination. In the crystal, the molecular organization was further stabilized by well-defined weak hydrogen bonding interactions between the neutral dinuclear molecular units that led to the formation of a three-dimensional network. The fluorescence properties of the two complexes 1 and 2 in organic solvents were also studied. The results show that the ligand acetate favored energy transfer to the emitting energy level of Tb(Ⅲ) in complex 1. Some factors that influence the fluorescent intensity were also discussed in the article. Two dinuclear compounds [Ln2(acetate)6(H2O)4]-4H2O (Ln=Tb(1), Sm(2)) were obtained by the hydrothermal reaction of Ln2O3 with malonic acid at 150 ℃. Both compounds were characterized by elemental analyses, infrared spectra, and single crystal X-ray diffraction. The results showed that complexes 1 and 2 were isomorphous and crystallize in triclinic space group P 1. The coordination geometry around Ln(Ⅲ) ions in the complexes 1 and 2 was a distorted tricapped trigonal prism with a nine coordination. In the crystal, the molecular organization was further stabilized by well-defined weak hydrogen bonding interactions between the neutral dinuclear molecular units that led to the formation of a three-dimensional network. The fluorescence properties of the two complexes 1 and 2 in organic solvents were also studied. The results show that the ligand acetate favored energy transfer to the emitting energy level of Tb(Ⅲ) in complex 1. Some factors that influence the fluorescent intensity were also discussed in the article.
出处 《Journal of Rare Earths》 SCIE EI CAS CSCD 2008年第2期178-184,共7页 稀土学报(英文版)
基金 the National Natural Science Foundation of China (20772037) the Natural Science Foundation of Guangdong Province (06025033)
关键词 rare earth dinuclear complexes X-ray crystal structure malonic acid fluorescence rare earths rare earth dinuclear complexes X-ray crystal structure malonic acid fluorescence rare earths
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