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六硝酸钕离子液体的合成、结构及近红外光致发光

Synthesis, structure and near-infrared photoluminescence of hexanitratoneodymate ionic liquids.

作者信息

He Ling, Ji Shun-Ping, Tang Ning, Zhao Ying, Tao Guo-Hong

机构信息

College of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China.

出版信息

Dalton Trans. 2015 Feb 7;44(5):2325-32. doi: 10.1039/c4dt03294b.

Abstract

Five hexanitratoneodymate-based rare earth complexes () were synthesized using a straightforward method. Purple plate crystals of were isolated and the crystal structure was determined by single-crystal X-ray diffraction with respect to the coordination mode of the nitrate anion to the central Nd(iii) ion. (: monoclinic system P21/c, a = 15.9460(3) Å, b = 10.2457(6) Å, c = 33.323(3) Å, β = 91.8108(17)°, V = 3109.11(11) Å(3), Z = 4). The central Nd(iii) ion is surrounded by six bidentate nitrate ligands, with a major trend towards high symmetry of the Nd(NO3)6 anion as an icosahedron. Thermal properties were determined from differential scanning calorimetry (DSC) combined with thermogravimetric analysis (TGA) tests. Complexes are found to be room temperature liquids, and their excitation and emission spectra were recorded. These complexes exhibit intense near-infrared (NIR) luminescence emission, which originates from interconfigurational f-f transitions (4)F3/2→(4)IJ multiplet (J = 9/2-13/2). These liquid Nd(iii) complexes are of interest as potential NIR luminescent soft materials with high thermal stability.

摘要

采用一种简单的方法合成了五种基于六硝酸钕的稀土配合物()。分离出了紫色片状晶体,并通过单晶X射线衍射确定了其晶体结构,涉及硝酸根阴离子与中心Nd(III)离子的配位模式。(:单斜晶系P21/c,a = 15.9460(3) Å,b = 10.2457(6) Å,c = 33.323(3) Å,β = 91.8108(17)°,V = 3109.11(11) Å(3),Z = 4)。中心Nd(III)离子被六个双齿硝酸根配体包围,Nd(NO3)6阴离子具有向二十面体高对称性发展的主要趋势。通过差示扫描量热法(DSC)结合热重分析(TGA)测试确定了热性质。发现配合物在室温下为液体,并记录了它们的激发和发射光谱。这些配合物表现出强烈的近红外(NIR)发光发射,其源于组态间f-f跃迁(4)F3/2→(4)IJ多重态(J = 9/2 - 13/2)。这些液态Nd(III)配合物作为具有高热稳定性的潜在近红外发光软材料具有研究价值。

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