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3-巯基丙酸根合钆(III)、铕(III)和铽(III)配合物的结构研究与荧光性质。

Structural investigation and photoluminescent properties of gadolinium(III), europium(III) and terbium(III) 3-mercaptopropionate complexes.

机构信息

Laboratory of Functional Materials - Institute of Chemistry, University of Campinas - UNICAMP, Campinas, SP, 13083-970, Brazil.

出版信息

J Fluoresc. 2014 Jan;24(1):203-11. doi: 10.1007/s10895-013-1288-5. Epub 2013 Aug 18.

Abstract

This work reports on the synthesis, crystallographic determination and spectroscopic characterization of gadolinium(III), terbium(III) and europium(III) 3-mercaptopropionate complexes, aqua-tris(3-mercaptopropionate)lanthanide(III)--[Ln(mpa)3(H2O)]. The Judd-Ofelt intensity parameters were experimentally determined from emission spectrum of the [Eu(mpa)3(H2O)]complex and they were also calculated from crystallographic data. The complexes are coordination polymers, where the units of each complex are linked together by carboxylate groups leading to an unidimensional and parallel chains that by chemical interactions form a tridimensional framework. The emission spectrum profile of the [Eu(mpa)3(H2O)] complex is discussed based on point symmetry of the europium(III) ion, that explains the bands splitting observed in its emission spectrum. Photoluminescent analysis of the [Gd(mpa)3(H2O)] complex show no efficient ligand excitation but an intense charge transfer band. The excitation spectra of the [Eu(mpa)3(H2O)] and [Tb(mpa)3(H2O)] complexes do not show evidence of energy transfer from the ligand to the excited levels of these trivalent ions. Therefore the emission bands are originated only by direct f-f intraconfigurational excitation of the lantanide(III) ions.

摘要

本工作报道了镝(III)、铽(III)和铕(III) 3-巯基丙酸配合物、水合三(3-巯基丙酸)镧系元素(III)--[Ln(mpa)3(H2O)]的合成、晶体结构测定和光谱表征。从[Eu(mpa)3(H2O)]配合物的发射光谱实验确定了 Judd-Ofelt 强度参数,并从晶体学数据计算得到了它们。这些配合物是配位聚合物,每个配合物的单元通过羧酸基团连接在一起,形成一维平行链,通过化学相互作用形成三维框架。基于镝(III)离子的点对称性讨论了[Eu(mpa)3(H2O)]配合物的发射光谱轮廓,解释了其发射光谱中观察到的带分裂。[Gd(mpa)3(H2O)]配合物的光致发光分析表明,没有有效的配体激发,但存在强烈的电荷转移带。[Eu(mpa)3(H2O)]和[Tb(mpa)3(H2O)]配合物的激发光谱没有证据表明从配体到这些三价离子的激发态发生能量转移。因此,发射带仅源于镧系元素(III)离子的直接 f-f 内组态激发。

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