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带 EDA 核的阴离子磺化和羧化 PPI 树状大分子:选择性金属络合剂的合成与表征。

Anionic sulfonated and carboxylated PPI dendrimers with the EDA core: synthesis and characterization of selective metal complexing agents.

机构信息

Departamento de Química Inorgánica, Universidad de Alcalá, Campus Universitario, E-28871 Alcalá de Henares, Spain.

出版信息

Dalton Trans. 2013 Apr 28;42(16):5874-89. doi: 10.1039/c3dt32870h.

DOI:10.1039/c3dt32870h
PMID:23462972
Abstract

Herein we describe the synthesis and characterization of new sulfonated and carboxylated poly(propyleneimino) (PPI) dendrimers with the ethylenediamino (EDA) core, at generations 1, 2 and 3. By means of UV-Vis and EPR spectroscopy, using Cu(2+) as a probe, we concluded that these dendrimers show a specific pattern in the coordination of metal ions. In agreement with the UV-Vis studies, EPR spectra of carboxylated compounds are constituted by 3 different signals which appear and then disappear with increasing copper concentration, corresponding to the saturation of different copper complexation sites. At the lowest copper concentration up to a 1:1 molar ratio between Cu(II) and the dendrimer, the spectrum is characteristic of a CuN2O2 coordination at the core of the dendrimer. The spectrum appearing at higher Cu(II) concentrations indicates a peripheral location of the ions coordinating one nitrogen and 3 oxygen atoms in a square planar geometry in restricted mobility conditions. For the highest concentrations tested, copper ions are confined at the external dendrimer surface with CuO4 coordination. For sulfonate systems, the EPR results are in line with a weaker interaction of Cu(II) with the nitrogen sites and a stronger interaction with the oxygen (SO3(-)) groups with respect to the interactions measured by EPR for carboxylate systems.

摘要

在此,我们描述了新型磺化和羧化聚(亚丙基亚胺)(PPI)树状大分子的合成与表征,其核心为乙二胺(EDA),代数为 1、2 和 3。通过使用 Cu(2+) 作为探针的紫外可见光谱和电子顺磁共振(EPR)光谱,我们得出结论,这些树状大分子在金属离子的配位中表现出特定的模式。与紫外可见研究一致,羧化化合物的 EPR 光谱由 3 个不同的信号组成,这些信号随着铜浓度的增加而出现和消失,对应于不同的铜络合位点的饱和。在最低的铜浓度下,直到 Cu(II) 和树状大分子之间的摩尔比达到 1:1,光谱特征为铜在树状大分子核心的 N2O2 配位。在更高的 Cu(II)浓度下出现的光谱表明,离子位于外围,以正方形平面几何构型在受限的迁移条件下配位一个氮原子和 3 个氧原子。对于测试的最高浓度,铜离子被限制在外部树状大分子表面,具有 CuO4 配位。对于磺酸酯系统,EPR 结果与 Cu(II)与氮位点的较弱相互作用以及与氧(SO3(-))基团的较强相互作用一致,与 EPR 测量的羧酸盐系统的相互作用相比。

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