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首页> 外文期刊>Inorganica Chimica Acta >Synthesis, crystalline structure and photoluminescence investigations of the new trivalent rare earth complexes (Sm3+, Eu3+ and Tb3+) containing 2-thiophenecarboxylate as sensitizer
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Synthesis, crystalline structure and photoluminescence investigations of the new trivalent rare earth complexes (Sm3+, Eu3+ and Tb3+) containing 2-thiophenecarboxylate as sensitizer

机译:含有2-噻吩羧酸盐作为敏化剂的新型三价稀土配合物(Sm3 +,Eu3 +和Tb3 +)的合成,晶体结构和光致发光研究

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New complexes with the general formula [RE(TPC)(3) (.) (H2O)(2)], where RE = Eu3+, Sm3+, Gd3+, Tb3+ and TPC = 2-thiophenecarboxylate, have been prepared and investigated by photoluminescence spectroscopy. These compounds were characterized by complexometric titration, elemental analyses and infrared spectroscopy. The X-ray crystal structure has been determined for the [Eu(TPC)(3) (.) (H2O)(2)] compound, indicating that this complex is in dimeric form bridged by two carboxylate ions with monoclinic crystal system and space group P2(1). The coordination polyhedron can be described as a distorted square antiprism, where six oxygen atoms belong to the TPC ligand and two oxygen atoms belong to the water molecules, with site symmetry close to C-2v. The theoretical value of the intensity parameter Omega(2), which is in agreement with the experimental one, indicates that the Eu3+ ion is in a highly polarizable chemical environment. Based on the luminescence spectra, the energy transfer from the ligand triplet state (T) of TPC to the excited levels of the Eu3+ ion is discussed. The emission quantum efficiency of the D-5(0) emitting level of the Eu3+ ion was also determined. In the case of the Tb3+ ion, the photoluminescence data show the high emission intensity of the characteristic transitions D-5(4) --> F-7(J) (J = 0-6), indicating that the TPC ligand is a good sensitizer. It is also noticed that the complexes with the Eu3+ and Tb3+ ions are more luminescent than the complex with the Sm3+ ion. (C) 2003 Elsevier B.V. All rights reserved. [References: 32]
机译:制备了具有通式[RE(TPC)(3)(。)(H2O)(2)]的新配合物,其中RE = Eu3 +,Sm3 +,Gd3 +,Tb3 +和TPC = 2-噻吩羧酸酯,并通过光致发光光谱法进行了研究。 。这些化合物通过络合滴定,元素分析和红外光谱进行表征。已确定[Eu(TPC)(3)(。)(H2O)(2)]化合物的X射线晶体结构,表明该络合物为二聚体形式,由两个具有单斜晶体系统和空间的羧酸根离子桥接组P2(1)/ n。配位多面体可以描述为扭曲的方形反棱镜,其中六个氧原子属于TPC配体,两个氧原子属于水分子,且位置对称性接近C-2v。强度参数Omega(2)的理论值与实验值一致,表明Eu3 +离子处于高度可极化的化学环境中。基于发光光谱,讨论了从TPC的配体三重态(T)到Eu3 +离子激发能级的能量转移。还确定了Eu3 +离子的D-5(0)发射能级的发射量子效率。在Tb3 +离子的情况下,光致发光数据显示特征转变D-5(4)-> F-7(J)(J = 0-6)的高发射强度,表明TPC配体是好敏化剂。还应注意,与Eu3 +和Tb3 +离子形成的配合物比与Sm3 +离子形成的配合物更发光。 (C)2003 Elsevier B.V.保留所有权利。 [参考:32]

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