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具有新型配体N-(萘-2-基)-N-苯基-2-(喹啉-8-基氧基)乙酰胺的稀土配合物:制备与光谱研究

Rare earth complexes with a novel ligand N-(naphthalen-2-yl)-N-phenyl-2-(quinolin-8-yloxy)acetamide: preparation and spectroscopic studies.

作者信息

Wu Wei-Na, Tang Ning, Yan Lan

机构信息

College of Chemistry and Chemical Engineering and State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, PR China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2008 Dec 15;71(4):1461-5. doi: 10.1016/j.saa.2008.05.001. Epub 2008 May 13.

Abstract

Six complexes of rare earth nitrates (Ln=La, Sm, Eu, Gd, Tb, Dy) with a new amide type ligand, N-(naphthalen-2-yl)-N-phenyl-2-(quinolin-8-yloxy)acetamide (L) have been prepared and characterized by elemental analysis, conductivity measurements, IR and and 1H NMR spectra. Under excitation, Eu(III) and Sm(III) complexes exhibited strong red emissions. And the luminescence intensity of Sm(III) complex is higher than that of Eu(III) complex. Thus the Eu(III) and Sm(III) complexes are the potential light conversion agent. However, the Tb(III) and Dy(III) complexes cannot exhibit characteristic emissions of terbium and dysprosium ions, respectively. The results of phosphorescence spectrum show that the triplet-state energy level of the ligand matches better to the resonance level of Eu(III) than Tb(III) ion. In addition, the luminescence of the Eu(III) complex is also relatively strong in highly diluted tetrahydrofuran solution (2 x 10(-4)mol/L) compared with the powder. This is not only due to the solvate effects but also to the changes of the structure of the Eu(III) complex after being dissolved into the solvents. Furthermore, owing to the co-luminescence effect, the proper La(III) or Gd(III) doped Eu(III) complexes show stronger luminescence than the pure Eu(III) complex.

摘要

制备了六种稀土硝酸盐配合物(Ln = La、Sm、Eu、Gd、Tb、Dy),其配体为一种新型酰胺类配体N-(萘-2-基)-N-苯基-2-(喹啉-8-氧基)乙酰胺(L),并通过元素分析、电导率测量、红外光谱和1H NMR光谱对其进行了表征。在激发下,Eu(III)和Sm(III)配合物表现出强烈的红色发射。并且Sm(III)配合物的发光强度高于Eu(III)配合物。因此,Eu(III)和Sm(III)配合物是潜在的光转换剂。然而,Tb(III)和Dy(III)配合物分别不能表现出铽离子和镝离子的特征发射。磷光光谱结果表明,配体的三重态能级与Eu(III)的共振能级比与Tb(III)离子的共振能级匹配得更好。此外,与粉末相比,Eu(III)配合物在高度稀释的四氢呋喃溶液(2×10(-4)mol/L)中的发光也相对较强。这不仅归因于溶剂化效应,还归因于Eu(III)配合物溶解到溶剂后结构的变化。此外,由于共发光效应,适当掺杂La(III)或Gd(III)的Eu(III)配合物比纯Eu(III)配合物表现出更强的发光。

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