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设计并合成了一系列一维镧系配位聚合物,表现出发光和磁化缓慢弛豫的性质。

Design and synthesis of a family of 1D-lanthanide-coordination polymers showing luminescence and slow relaxation of the magnetization.

机构信息

Department of Chemistry and Physics, Research Centre CIAIMBITAL, University of Almería, Ctra. Sacramento s/n, 04120 Almería, Spain.

出版信息

Dalton Trans. 2018 Sep 18;47(36):12783-12794. doi: 10.1039/c8dt02592d.

Abstract

We have designed and synthesized eight isostructural 1D coordination polymers (CPs) with the general formula {[Ln(aapc)3(DMF)]}n [where Ln(iii) = Y (2), La (3), Nd (4), Eu (5), Gd (6), Tb (7), Dy (8), Er (9); and aapc = 3-((anthraquinone-1-yl)amino)propanoate]. These CPs consist of Ln-carboxylate infinite rods in which the bulky anthraquinone scaffolds arise from it in such a way that the resulting supramolecular packing exhibits isolated 1D chains. Solution structures have been corroborated through NMR methods including PGSE and EXSY NMR studies and, due to the presence of lanthanide ions, magnetic and luminescence properties have been studied. Alternating current magnetic measurements of compound 8 show slow relaxation of the magnetization, a characteristic of single molecule magnets (SMMs). The evaluation of solid-state photophysical properties reveals that the aapc scaffold sensitizes lanthanide(iii) based emission of compounds 4-9 both in the visible and near-infrared (NIR) regions at 10 K.

摘要

我们设计并合成了八个同构的 1D 配位聚合物(CPs),具有通式{[Ln(aapc)3(DMF)]}n [其中 Ln(iii) = Y(2)、La(3)、Nd(4)、Eu(5)、Gd(6)、Tb(7)、Dy(8)、Er(9);和 aapc = 3-((蒽醌-1-基)氨基)丙酸盐]。这些 CPs 由 Ln-羧酸酯无限棒组成,其中庞大的蒽醌支架以这样的方式出现,使得所得超分子堆积表现出孤立的 1D 链。通过包括 PGSE 和 EXSY NMR 研究在内的 NMR 方法证实了溶液结构,并且由于存在镧系元素离子,研究了磁和发光性质。化合物 8 的交流磁测量显示出磁化强度的缓慢弛豫,这是单分子磁体(SMM)的特征。固态光物理性质的评估表明,aapc 支架在可见和近红外(NIR)区域(10 K 时)均敏化化合物 4-9 的镧系元素(iii)发射。

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