荧光
化学
检出限
共价键
选择性
分子内力
水溶液中的金属离子
光化学
组合化学
甲壳素
密度泛函理论
离子
咪唑
质子
嫁接
生物传感器
槲皮素
喹啉
金属
共价有机骨架
无机化学
费斯特共振能量转移
锌
化学改性
线性范围
作者
Ruyi He,Xijun Wang,Meng Xiao He,Xiang Zhouyang,Yun Li,Haisong Qi
标识
DOI:10.1021/acssuschemeng.5c09463
摘要
This study reports the development of a sustainable solid-state fluorescent chemosensor for selective detection of zirconium ions (Zr4+) by covalently grafting quercetin onto chitin via a Mannich reaction. The chitin-quercetin (Ch-Q) film exhibits a distinct “turn-on” yellow-green fluorescence response at 540 nm upon Zr4+ binding, attributed to chelation-enhanced fluorescence (CHEF) and the suppression of excited-state intramolecular proton transfer (ESIPT). The sensor exhibits exceptional selectivity for Zr4+ over competing metal ions, along with a low detection limit (1.157 μM), rapid response (<60 s), and broad operational pH range (2–8). Density functional theory (DFT) calculations confirm the optimal Zr4+ binding site and elucidate the underlying ligand-to-metal charge transfer (LMCT) mechanism. This biomass-derived platform offers a simple, sustainable, and eco-friendly solution for real-time Zr4+ monitoring in environmental applications.
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