化学
过氯酸盐
高氯酸盐
配位聚合物
联吡啶
俘获
高分子化学
聚合物
无机化学
锝
有机化学
核化学
铼
晶体结构
生态学
生物
作者
Beatriz Ehlke,Cambell S. Conour,Tyler J. Vandiver,Kevin C. Lofgren,Jeremy L. Barnett,Eric W. Reinheimer,John S. Wenger,Scott R. J. Oliver
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-05-01
卷期号:63 (19): 8674-8684
被引量:1
标识
DOI:10.1021/acs.inorgchem.4c00202
摘要
Pertechnetate, the most stable form of the radionuclide 99Tc in aerobic aqueous systems, is a hazardous anion present in nuclear waste. Its high mobility in water makes the remediation of the anion challenging. In the past decade, significant effort has been placed into finding materials capable of adsorbing this species. Here, we present the synthesis and high-resolution crystal structure of the coordination polymer [Ag(2,4′-bipyridine)]NO3, which is capable of sequestering perrhenate─a pertechnetate surrogate─through anion exchange to form another new coordination polymer, [Ag(2,4′-bipyridine)]ReO4. Both the beginning and end structures were solved by single-crystal X-ray diffraction and the adsorption reaction was monitored through inductively coupled plasma-optical emission spectroscopy and UV–vis spectroscopy. The exchange reaction follows a pseudo-second-order mechanism and the maximum adsorption capacity is 764 mg ReO4/g [Ag(2,4′-bipyridine)]NO3, one of the highest recorded for a coordination polymer or metal–organic framework. A solvent-mediated recrystallization mechanism was determined by monitoring the ion-exchange reaction by scanning electron microscopy–energy-dispersive spectroscopy and powder X-ray diffraction.
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