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离子液体导向的耐碱锌金属有机框架用于水相中抗生素和硝基芳香族炸药的检测

Aqueous-phase detection of antibiotics and nitroaromatic explosives by an alkali-resistant Zn-MOF directed by an ionic liquid.

作者信息

Qin Jian-Hua, Huang Ya-Dan, Shi Ming-Yu, Wang Hua-Rui, Han Min-Le, Yang Xiao-Gang, Li Fei-Fei, Ma Lu-Fang

机构信息

College of Chemistry and Chemical Engineering, Henan Key Laboratory of Function-Oriented Porous Materials, Luoyang Normal University Luoyang 471934 China

College of Chemistry and Chemical Engineering, Henan Polytechnic University Jiaozuo 454000 PR. China.

出版信息

RSC Adv. 2020 Jan 8;10(3):1439-1446. doi: 10.1039/c9ra08733h. eCollection 2020 Jan 7.

DOI:10.1039/c9ra08733h
PMID:35494702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9047407/
Abstract

An alkali-resistant Zn-MOF directed by [BMI]Br ionic liquid, (BMI)[Zn(ptptc)] (1), based on a π-electron-rich terphenyl-tetracarboxylic acid, has been synthesized under the combination of hydro/solvothermal and ionothermal condition (BMI = 1-butyl-3-methylimidazolium, Hptptc = -terphenyl-3,3'',5,5''-tetracarboxylic acid). In 1, the trinuclear Zn(ii) clusters are linked by the organic moieties of the ptptc ligands, resulting in a 3D anionic framework structure with highly disordered [BMI] cations filled in the pores. 1 exhibits good chemical stability in water and NaOH solutions (pH range of 7-12), which allow it to detect antibiotics and nitroaromatic explosives in an aquatic system. 1 represents high fluorescence quenching efficiency toward NFs (furazolidone, FZD; nitrofurazone, NZF; nitrofurantoin, NFT), NMs (ronidazole, RDZ; metronidazole, MDZ; dimetridazole, DTZ; ornidazole, ODZ) and nitrophenol (2-nitrophenol, 2-NP; 3-nitrophenol, 3-NP; 4-nitrophenol, 4-NP; 2,4,6-trinitrophenol, TNP) in water solution, respectively.

摘要

由[BMI]Br离子液体导向的一种耐碱锌基金属有机框架化合物(BMI)[Zn(ptptc)](1),基于富π电子的三联苯四羧酸,在水热/溶剂热和离子热条件相结合的情况下合成(BMI = 1-丁基-3-甲基咪唑鎓,Hptptc = 三联苯-3,3'',5,5''-四羧酸)。在化合物1中,三核Zn(ii)簇通过ptptc配体的有机部分相连,形成一种三维阴离子框架结构,孔隙中填充有高度无序的[BMI]阳离子。化合物1在水和NaOH溶液(pH范围为7 - 12)中表现出良好的化学稳定性,这使其能够在水生系统中检测抗生素和硝基芳香族炸药。化合物1对水溶液中的硝基呋喃类药物(呋喃唑酮,FZD;呋喃西林,NZF;呋喃妥因,NFT)、硝基咪唑类药物(甲硝唑,RDZ;甲硝唑,MDZ;二甲硝唑,DTZ;奥硝唑,ODZ)和硝基苯酚(2-硝基苯酚,2-NP;3-硝基苯酚,3-NP;4-硝基苯酚,4-NP;2,4,6-三硝基苯酚,TNP)分别表现出高荧光猝灭效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/31e9adf33f98/c9ra08733h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/4ae75f5f554a/c9ra08733h-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/c667c0a53b37/c9ra08733h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/963f16729be8/c9ra08733h-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/1cacd6381c21/c9ra08733h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/31e9adf33f98/c9ra08733h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/4ae75f5f554a/c9ra08733h-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/c667c0a53b37/c9ra08733h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/963f16729be8/c9ra08733h-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/1cacd6381c21/c9ra08733h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36c/9047407/31e9adf33f98/c9ra08733h-f4.jpg

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