Abstract

Immobilizing radioactive organic iodides (ROIs) is essential for radioactive-pollution remediation. However, conventional ROI sorbents often suffer from I<sup>-</sup> leakage, and the atomic-level mechanisms underlying ROI immobilization remain unclear. Herein, a reaction-induced postactivated nanotrap strategy is proposed for the leakage-resistant immobilization of trace-level methyl iodide. The nanotrap in a stable metal-organic framework (<b>SCU-365</b>) undergoes <i>in situ</i> activation by methylation during chemisorption and then precisely confines the generated I<sup>-</sup>, which enables the crystallographic visualization of chemisorbed ROI for the first time. Structural and computational analyses reveal that the synergy of multiple weak interactions for I<sup>-</sup> complexation rivals the strength of a covalent bond, endowing <b>SCU-365</b> with exceptional leakage resistance superior to that of state-of-the-art ROI sorbents. This work proposes a novel strategy for antileakage material design for nuclide sequestration and fills the gap of understanding how materials interact with ROI.

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Year
2025
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Zhiwei Li, Dan Zhou, Linwei He et al. (2025). Reaction-Induced Post-Activated Nanotrap Strategy for Leakage-Resistant Immobilization of Radioactive Organic Iodide. Journal of the American Chemical Society . https://doi.org/10.1021/jacs.5c15907

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DOI
10.1021/jacs.5c15907