化学
水溶液
吡嗪
连接器
发光
硝基苯
沸石咪唑盐骨架
组合化学
微型多孔材料
金属有机骨架
咪唑酯
光化学
有机化学
无机化学
立体化学
操作系统
催化作用
计算机科学
吸附
光电子学
物理
作者
Fei‐Long Luo,Haobo Wang,Kun Wu,Dong Luo,Yifang Zhao,Yong‐Liang Huang,Weigang Lu
标识
DOI:10.1021/acs.inorgchem.5c01125
摘要
By employing a mix-linker strategy, we have successfully synthesized two isostructural anionic microporous biological metal-organic frameworks (Bio-MOFs), showing excellent chemical stability across a pH range of 3-14 in the aqueous phase. Luminescence titration studies reveal that replacing the benzene core of the carboxylate linker with pyrazine leads to markedly enhanced energy transfer from the linker to the metal cluster, significantly increasing the emission intensity. This linker engineering strategy endows the MOF with superior performance in antibiotic sensing with limits of detection of 1.5 μM for colchicine (COL) and 0.8 μM for nitrofurazone (NFZ). Additionally, the title MOF exhibited selective detection of COL and NFZ in the presence of potential interfering species, including other antibiotics or serum species. Moreover, a mixed matrix film was fabricated by dispersing the MOF crystalline powders on a polycaprolactone sheet, demonstrating real-time on-site monitoring of COL and NFZ in aqueous solutions.
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