Polido Legaria Elizabeth, Topel Seda Demirel, Kessler Vadim G, Seisenbaeva Gulaim A
Department of Chemistry and Biotechnology, BioCenter, Swedish University of Agricultural Sciences, Box 7015, 75007 Uppsala, Sweden.
Dalton Trans. 2015 Jan 21;44(3):1273-82. doi: 10.1039/c4dt03096f.
The binding and release of trivalent rare earth element (REE) cations (Dy(3+), Nd(3+) and La(3+)) from solutions by a new fully characterized magnetic nano adsorbent material, consisting of iminodiacetic acid ligand (H2IDA) grafted onto SiO2 covered γ-Fe2O3 nanoparticles, was investigated. The nano adsorbent revealed a slightly higher capacity towards heavier REE and appreciable selectivity, especially on desorption. It was found that the composition of the surface complex was RE(3+) : L = 1 : 1. The complexation of the molecular H2IDA with RE(3+) in this ratio under non-basic conditions was therefore investigated by X-ray crystallography to produce relevant molecular models. Unexpectedly big differences in coordination numbers and binding mode of IDA along with distinct analogies in packing of the ligand molecules in the obtained 2D-coordination polymer structures provided valuable insights into possible reasons for the observed selectivity.
研究了一种新型的、具有完全表征的磁性纳米吸附材料对三价稀土元素(REE)阳离子(Dy(3+)、Nd(3+)和La(3+))的吸附和解吸情况。该材料由接枝在SiO2包覆的γ-Fe2O3纳米颗粒上的亚氨基二乙酸配体(H2IDA)组成。这种纳米吸附剂对较重的REE显示出稍高的吸附容量和可观的选择性,特别是在解吸方面。研究发现表面络合物的组成是RE(3+) : L = 1 : 1。因此,通过X射线晶体学研究了在非碱性条件下分子H2IDA与RE(3+)以该比例的络合情况,以生成相关的分子模型。所得二维配位聚合物结构中IDA的配位数和结合模式存在意想不到的巨大差异,以及配体分子堆积方面的明显相似性,为观察到的选择性的可能原因提供了有价值的见解。