摘要
A new lanthanide formate oxalate framework [Eu（C2O4）（HCOO）]n （1） has been synthesized via hydrothermal method and characterized by single-crystal X-ray diffraction （SC-XRD）. The framework crystallizes in the orthorhombic Pnma space group, with a = 7.0984（4）, b = 6.6442（3）, c = 10.6793（6） ？, V = 503.68（4） ？3, Z = 3, C3HO6Eu, Mr = 285.00 g/mol, Dc = 3.7581 g/cm3, F（000） = 520.3796, μ = 12.413 mm-1, the final R = 0.0264 and wR = 0.0628 for 797 observed reflections with I 〉 2σ（I）. The photoluminescence （PL） measurements reveal the significant red emission of the framework is dominated by the （5D0 → 7F2） electronic transition at 614 nm. Further variable-temperature powder X-ray diffraction （VT-PXRD） indicates that framework 1 shows slight negative thermal expansion （NTE） along the a-axis, and positive thermal expansion （PTE） along the b and c axes.
A new lanthanide formate oxalate framework [Eu（C2O4）（HCOO）]n （1） has been synthesized via hydrothermal method and characterized by single-crystal X-ray diffraction （SC-XRD）. The framework crystallizes in the orthorhombic Pnma space group, with a = 7.0984（4）, b = 6.6442（3）, c = 10.6793（6） ？, V = 503.68（4） ？3, Z = 3, C3HO6Eu, Mr = 285.00 g/mol, Dc = 3.7581 g/cm3, F（000） = 520.3796, μ = 12.413 mm-1, the final R = 0.0264 and wR = 0.0628 for 797 observed reflections with I 〉 2σ（I）. The photoluminescence （PL） measurements reveal the significant red emission of the framework is dominated by the （5D0 → 7F2） electronic transition at 614 nm. Further variable-temperature powder X-ray diffraction （VT-PXRD） indicates that framework 1 shows slight negative thermal expansion （NTE） along the a-axis, and positive thermal expansion （PTE） along the b and c axes.
基金
supported by the National Natural Science Foundation of China(21571072)
