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配体调控三种基于锌(II)的配位聚合物的不同结构以用于抗生素降解。

Ligand Modulation on the Various Structures of Three Zinc(II)-Based Coordination Polymers for Antibiotics Degradation.

机构信息

School of Chemistry and Environmental Engineering, Sichuan University of Science & Engineering, Zigong 643000, China.

Department of Chemistry, Berhampur University, Berhampur 760007, India.

出版信息

Molecules. 2023 Mar 24;28(7):2933. doi: 10.3390/molecules28072933.

DOI:10.3390/molecules28072933
PMID:37049696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10095641/
Abstract

The efficient removal of organic contaminants from wastewater is, nowadays, a prominent area of study due to its biological as well as environmental significance. Antibiotics are now found in wastewater because of their high use, which has become a source of aquatic pollution. These antibiotics have dangerous implications for people's health. Hence, effective pharmaceutical removal from wastewater and contaminated water bodies, especially the removal of antibiotics, is of major interest to global research organizations. This is why it is necessary to investigate this class of toxic material in wastewater discharge. We synthesized three different coordination polymers (CPs) in the presence of various assistant carboxylate linkers, namely, [Zn(Hbtc)(dip)] (), [Zn(1,2-bdc)(dip)] (), and [Zn(1,4-bdc)(dip)] () (3,5-di(1H-imidazol-1-yl)pyridine = dip, 1,3,5-benzenetricarboxylic acid = Hbtc, 1,2-benzenedicarboxylic acid = 1,2-Hbdc, and 1,4-benzendicarboxylic acid = 1,4-bdc). These CPs were characterized by using different techniques, including single-crystal X-ray diffraction. The structural studies demonstrated that in , there are four Zn(II) centers and both centers are in different coordination environments (Zn2 has distorted tetrahedral geometry, whereas Zn1, Zn3, and Zn4 have square pyramidal geometry). Hirshfeld surfaces analysis revealed that different types of intermolecular interactions (C⋯C, H⋯C, H⋯H, O⋯C, N⋯H, and O⋯H) are present in the synthesized CPs. We examined the different antibiotics, such as metronidazole (MDZ), nitrofurazone (NFZ), dimetridazole (DTZ), sulfasalazine(SLA), and oxytetracycline (OXY), degradation behaviors of the synthesized CPs, which showed remarkable degradation efficiency. showed photocatalytic behavior toward the NFZ antibiotic in an aqueous media. This study also showed that these catalysts are stable and reusable under mild conditions.

摘要

从废水高效去除有机污染物是目前生物和环境意义上的一个重要研究领域。由于抗生素的高使用率,现在在废水中也能发现抗生素,这已经成为了水环境污染的一个源头。这些抗生素对人们的健康有危险的影响。因此,从废水中和受污染的水体中有效去除药物,特别是去除抗生素,是全球研究机构的主要关注点。这就是为什么有必要调查废水中这类有毒物质的原因。

我们在存在不同辅助羧酸连接体的情况下合成了三种不同的配位聚合物(CPs),即[Zn(Hbtc)(dip)](),[Zn(1,2-bdc)(dip)]()和[Zn(1,4-bdc)(dip)]()(3,5-二(1H-咪唑-1-基)吡啶=dip,1,3,5-苯三甲酸=Hbtc,1,2-苯二甲酸=1,2-Hbdc,1,4-苯二甲酸=1,4-bdc)。这些 CPs 是通过使用不同的技术,包括单晶 X 射线衍射来表征的。结构研究表明,在中,有四个 Zn(II)中心,并且两个中心处于不同的配位环境(Zn2 具有扭曲的四面体形几何形状,而 Zn1、Zn3 和 Zn4 具有四方锥几何形状)。Hirshfeld 表面分析表明,在合成的 CPs 中存在不同类型的分子间相互作用(C⋯C、H⋯C、H⋯H、O⋯C、N⋯H 和 O⋯H)。我们研究了不同的抗生素,如甲硝唑(MDZ)、呋喃西林(NFZ)、二甲硝唑(DTZ)、柳氮磺胺吡啶(SLA)和土霉素(OXY),合成的 CPs 对这些抗生素的降解行为表现出了显著的降解效率。表现出对 NFZ 抗生素在水介质中的光催化行为。这项研究还表明,这些催化剂在温和条件下是稳定且可重复使用的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/f2de40cfabd2/molecules-28-02933-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/be701ddc0f7d/molecules-28-02933-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/7c62539c0bd5/molecules-28-02933-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/5c7542d8472b/molecules-28-02933-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/6c5210c51455/molecules-28-02933-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/384ad529176c/molecules-28-02933-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/401e57ddc0e6/molecules-28-02933-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/92eed3d97e18/molecules-28-02933-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/83c23782208a/molecules-28-02933-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/f2de40cfabd2/molecules-28-02933-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/be701ddc0f7d/molecules-28-02933-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/7c62539c0bd5/molecules-28-02933-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/5c7542d8472b/molecules-28-02933-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/6c5210c51455/molecules-28-02933-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/384ad529176c/molecules-28-02933-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/401e57ddc0e6/molecules-28-02933-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/92eed3d97e18/molecules-28-02933-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/83c23782208a/molecules-28-02933-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b74/10095641/f2de40cfabd2/molecules-28-02933-g007.jpg

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