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March 23, 2026Inorganic Chemistry0 citations

Iodine Capture and Transformation at a Hydrogen-Bond-Stabilized Dimethylammonium Site within a Uranyl-Based MOF

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ZWZimeng WangJLJing LiaoXFXuan Fu

Key Points

  • The aim is to develop a material for efficiently capturing radioactive iodine using a uranyl-based MOF.
  • Synthesis of IHEP-103 via solvothermal process.
  • Combination of Schiff base ligands with uranyl cations.
  • Characterization using XPS, Raman spectroscopy, and single-crystal X-ray diffraction.
  • IHEP-103 demonstrates enhanced iodine adsorption through dimethylammonium cation interactions.
  • Iodine species evolve from the (I2·I3)- complex to polyiodide anions I5-.
  • Structural features of IHEP-103 contribute to its effectiveness in trapping iodine.

Abstract

Due to its high volatility and long half-life, iodine poses a serious threat to the environment and human health. Therefore, trapping radioactive iodine is of significant importance. In this study, a novel uranyl-based metal-organic framework (MOF) material, IHEP-103, was synthesized via a solvothermal process by combining Schiff base ligands with uranyl cations. IHEP-103 features 1D rhombic channels functionalized by dimethylamine, uranyl acyl oxygen atoms, imine nitrogen atoms, aromatic rings, and alkyl hydrogen moieties. The structural characteristics of IHEP-103 (such as its multiple functional groups) give it potential applications in iodine capture, while the dimethylammonium cation further enhances iodine adsorption through electrostatic interactions and intermolecular C-H···I interactions. The results from XPS, Raman spectroscopy, and single-crystal X-ray diffraction reveal an evolution of the iodine species surrounding the dimethylamine group with increasing iodine loading: from the (I2·I3)- supramolecular complex structure to the polyiodide anions I5-.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/69c0de74fddb9876e79c1436https://doi.org/10.1021/acs.inorgchem.6c00748
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