TY - JOUR
T1 - Tailoring Electron-Rich Fluorescent Supramolecular Organic Frameworks for Efficient Capture and Visual Monitoring of Iodine
AU - Li, Qiang
AU - Guo, Wenfeng
AU - Wang, Zijian
AU - Tan, Li Li
AU - Shang, Li
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/1/15
Y1 - 2025/1/15
N2 - The efficient capture and monitor of radioactive iodine are crucial for managing radioactive nuclear waste and protecting human health. Herein, three metal–organic coordination compound-mediated supramolecular organic frameworks (MSOFs) are reported with distinct electron-rich structures for efficient iodine capture with fluorescence response. The electron-rich adsorption sites play crucial roles for electron-deficient iodine capture via charge transfer interactions, where π donors contribute greater than nitrogen heteroatom. Among three MSOFs, MSOF-3 with the maximum numbers of electron-rich π donors exhibited the highest iodine uptake capacity (3.70 g mmol−1). Prominently, the charge transfer interactions between iodine and MSOFs result in distinct fluorescence response during iodine uptake, establishing a real-time fluorescence monitoring system. To facilitate the personal health protection toward practical application, a mask with high iodine removal efficiency (99.1%) and real-time fluorescence response is successfully developed. This study underscores the great promise of electron-rich fluorescent MSOFs for capture and sensing of radioactive iodine, offering substantial prospects for the advance of protective equipment in the nuclear industry.
AB - The efficient capture and monitor of radioactive iodine are crucial for managing radioactive nuclear waste and protecting human health. Herein, three metal–organic coordination compound-mediated supramolecular organic frameworks (MSOFs) are reported with distinct electron-rich structures for efficient iodine capture with fluorescence response. The electron-rich adsorption sites play crucial roles for electron-deficient iodine capture via charge transfer interactions, where π donors contribute greater than nitrogen heteroatom. Among three MSOFs, MSOF-3 with the maximum numbers of electron-rich π donors exhibited the highest iodine uptake capacity (3.70 g mmol−1). Prominently, the charge transfer interactions between iodine and MSOFs result in distinct fluorescence response during iodine uptake, establishing a real-time fluorescence monitoring system. To facilitate the personal health protection toward practical application, a mask with high iodine removal efficiency (99.1%) and real-time fluorescence response is successfully developed. This study underscores the great promise of electron-rich fluorescent MSOFs for capture and sensing of radioactive iodine, offering substantial prospects for the advance of protective equipment in the nuclear industry.
KW - electron-rich adsorption sites
KW - fluorescence response
KW - health protection
KW - iodine capture
KW - supramolecular organic frameworks
UR - http://www.scopus.com/inward/record.url?scp=85203435805&partnerID=8YFLogxK
U2 - 10.1002/adfm.202413694
DO - 10.1002/adfm.202413694
M3 - 文章
AN - SCOPUS:85203435805
SN - 1616-301X
VL - 35
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 3
M1 - 2413694
ER -