光致变色
小提琴手
金属有机骨架
化学
金属
抗生素
光化学
纳米技术
环境化学
组合化学
材料科学
有机化学
生物化学
吸附
作者
Shi Zhang,Yanping Zhao,Yudie Zhou,Qingfu Zhang,Xinyuan Zhang,Ziheng Xu,Guojian Chen,Kecai Xiong,Yanli Gai
标识
DOI:10.1021/acs.cgd.4c00765
摘要
A viologen-functionalized europium-based metal–organic framework, denoted as compound 1, has been synthesized solvothermally by employing 1,1′-bis(3,5-dicarboxyphenyl)-4,4′-bipyridinium dichloride (abbreviated as H4bdcbpCl2). Compound 1 possesses a 2-fold parallel self-interpenetrating structure composed of two sets of identical three-dimensional (3D) cationic frameworks with {4·84·12}2{42·82·102}{8}2 topology. The introduction of tetracarboxylic group-decorated viologen derivative not only facilitates the formation of a helix-based structure with high dimensionality and positively charged framework but also promotes the photoinduced electron transfer (PET)-caused photochromic property. Significantly, compound 1 demonstrates a rapid detection process for nitrofurantoin (NFT) and nitrofurazone (NFZ) in aqueous environments, exhibiting good recycling stability, large quenching coefficient (Ksv), low limit of detection (LOD), and high anti-interference ability through a fluorescence turn-off mechanism. This phenomenon was further investigated through spectroscopic analyses and density functional theory (DFT) calculations. Moreover, compound 1 also exhibits sensing capabilities for various ions in aqueous system, including Fe3+, Cr2O72–, and MnO4–, which further verify that compound 1 could serve as a multifunctional fluorescence sensor for molecular and ionic pollutants.
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