化学
锕系元素
钍
金属有机骨架
吸附
环己烷
碘酸盐
双功能
检出限
碘化物
碘
无机化学
金属
铀
放射化学
物理化学
有机化学
色谱法
核物理学
催化作用
物理
作者
Yu Ju,Zi‐Jian Li,Jie Qiu,Xiaoyun Li,Junpu Yang,Zhi‐Hui Zhang,Ming‐Yang He,Jian‐Qiang Wang,Jian Lin
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-05-15
卷期号:62 (21): 8158-8165
被引量:23
标识
DOI:10.1021/acs.inorgchem.3c00473
摘要
Actinide-bearing metal–organic frameworks (MOFs) encompass intriguing structures and properties, but the radioactivity of actinide cripples their applications. Herein, we have constructed a new thorium-based MOF (Th-BDAT) as a bifunctional platform for the adsorption and detection of radioiodine, a more radioactive fission product that can readily spread through the atmosphere in its molecular form or via solution as anionic species. The iodine capture within the framework of Th-BDAT from both the vapor phase and the cyclohexane solution has been verified, showing that Th-BDAT features maximum I2 adsorption capacities (Qmax) of 959 and 1046 mg/g, respectively. Notably, the Qmax of Th-BDAT toward I2 from cyclohexane solution ranks among the highest value for Th-MOFs reported to date. Furthermore, incorporating highly extended and π-electron-rich BDAT4– ligands renders Th-BDAT as a luminescent chemosensor whose emission can be selectively quenched by iodate with a detection limit of 1.367 μM. Our findings thus foreshadow promising directions that might unlock the full potential of actinide-based MOFs from the point of view of practical application.
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