铀酰
铀
螯合作用
化学
取代基
组合化学
海水
锕系元素
氢键
多孔性
材料科学
核化学
分子
无机化学
有机化学
海洋学
冶金
地质学
作者
Qi Sun,Briana Aguila,Jason A. Perman,Aleksandr S. Ivanov,Vyacheslav S. Bryantsev,Lyndsey D. Earl,Carter W. Abney,Łukasz Wojtas,Shengqian Ma
标识
DOI:10.1038/s41467-018-04032-y
摘要
Nature can efficiently recognize specific ions by exerting second-sphere interactions onto well-folded protein scaffolds. However, a considerable challenge remains to artificially manipulate such affinity, while being cost-effective in managing immense amounts of water samples. Here, we propose an effective approach to regulate uranyl capture performance by creating bio-inspired nano-traps, illustrated by constructing chelating moieties into porous frameworks, where the binding motif's coordinative interaction towards uranyl is enhanced by introducing an assistant group, reminiscent of biological systems. Representatively, the porous framework bearing 2-aminobenzamidoxime is exceptional in sequestering high uranium concentrations with sufficient capacities (530 mg g-1) and trace quantities, including uranium in real seawater (4.36 mg g-1, triple the benchmark). Using a combination of spectroscopic, crystallographic, and theory calculation studies, it is revealed that the amino substituent assists in lowering the charge on uranyl in the complex and serves as a hydrogen bond acceptor, boosting the overall uranyl affinity of amidoxime.
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