一种基于噻唑烷酮的新型生物活性偶氮染料,用于裸眼比色检测氰化物离子

IF 0.7 4区 化学 Q4 CHEMISTRY, ORGANIC Letters in Organic Chemistry Pub Date : 2024-01-25 DOI:10.2174/0115701786278059231122061237
Zahra Zamiraei, Kurosh Rad-Moghadam
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引用次数: 0

摘要

:设计并合成了一种嵌入噻唑烷酮杂环核心的新型生物活性偶氮染料,用于抗菌和有机溶液中氰离子(CNˉ)的比色感应。通过 1H NMR、FT-IR 和 UV-vis 光谱数据阐明了所制备染料的结构。事实证明,它是一种用于检测 CNˉ 的快速、灵敏的显色传感器。为了研究不同浓度的 CNˉ 对检测效率的影响,还进行了光谱研究。此外,研究表明,其他阴离子对合成染料检测 CNˉ 的灵敏度没有明显的竞争或影响。约伯图显示,染料和 CNˉ 在它们的彩色复合物中的化学计量为 1:1。通过使用涂有染料的纤维素纸,进一步开发了肉眼检测低浓度水溶液中 CNˉ 的方法。所制备的检测纸可在低至 2 μM 的浓度下感知 CNˉ。使用井扩散技术对该染料的抗菌活性进行评估后发现,其对区域试验中使用的细菌菌株的抑制活性至少与氨苄西林相当,在某些情况下甚至优于氨苄西林。在 CN¯ 的作用下,染料的颜色从黄色变为红棕色,这说明它与 CNˉ 发生了显著的相互作用,并提供了一种无需借助任何光谱仪器的肉眼感应方法:氰离子是一种严重的工业废水污染物,对哺乳动物有剧毒:设计并合成了一种嵌入噻唑烷酮杂环核心的新型生物活性偶氮染料,用于抗菌和有机溶液中氰离子的比色传感:通过 1H NMR、FTIR 和 UV-vis 光谱确认了所制备染料的结构。结果:......。针对 CN'离子,光谱研究了合成染料在与其他阴离子和不同浓度的氰离子竞争时与氰离子的相互作用。约伯图的结果表明,合成染料与 CN¯ 离子的化学结合比为 1:1。通过使用涂有染料的纤维素纸,进一步发展了肉眼检测低浓度水溶液中氰离子的方法。所制备的检测纸可在 2 µM 的浓度下感知 CN¯。使用井扩散技术对该染料的抗菌活性进行评估后发现,其对区域检测中使用的细菌菌株的抑制活性至少与氨苄西林相当,在某些情况下甚至优于氨苄西林。
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A New Bioactive Thiazolidinone-based Azo Dye for Naked-eye Colorimetric Detection of Cyanide Ions
: A new bioactive azo dye embedding a thiazolidinone heterocyclic core was designed and synthesized for antibacterial application and colorimetric sensing of cyanide ion (CNˉ) in organic solutions. The structure of the prepared dye was elucidated from its 1H NMR, FT-IR and UV–vis spectral data. It proved to be a fast and sensitive colorogenic sensor for detection of CNˉ. Spectroscopic studies were carried out to investigate the effect of different CNˉ concentrations on the detection efficiency. Moreover, the studies revealed no significant competition or influence of other anions on sensitivity of CNˉ detection by the synthesized dye. A Job's plot indicated a 1:1 stoichiometry of the dye and CNˉ in their colorful complex. Further development of the method for naked-eye detection of CNˉ in low-concentration aqueous solutions was achieved by using the cellulose papers painted with the dye. The as-prepared testing paper allowed CNˉ sensing in concentrations as low as 2 μM. Evaluation of the dye for antibacterial activities using the well diffusion technique displayed that its inhibitory activity is at least as good as and in some cases superior to ampicillin against the bacterial strains employed in the zone assay. In response to CN¯, the dye changes color from yellow to reddish brown that accounts for its significant interactions with CNˉ and affords a naked-eye sensing method without resorting to any spectroscopic instrumentation. background: Cyanide ion is a serious pollutant of industrial wastewaters and is highly toxic for mammals. objective: A new bioactive azo dye embedding a thiazolidinone heterocyclic core was designed and synthesized for antibacterial application and colorimetric sensing of cyanide ions in organic solutions. method: The structures of prepared dyes were confirmed by 1H NMR, FTIR and UV–vis spectroscopies. It was found to be a fast and sensitive colorogenic sensor for detection of CN¯ ions. result: . In response to CN¯ ion, Spectroscopic studies were investigated of the interaction of synthesized dye with cyanide ion in competition with other anions and different concentrations of cyanide ion. The result of the Job's plot indicating that the stoichiometry binding ratios of synthesized dye and CN¯ is 1:1. Further development of the method for naked-eye detection of cyanide ion in low-concentration aquase solutions was achieved by using the cellulose papers painted with the dye. The as-prepared testing paper allowed CN¯ sensing in concentrations of 2 µM. Evaluation of the dye for antibacterial activities using the well diffusion technique displayed that its inhibitory activity is at least as good as and in some cases superior to ampicillin against the bacterial strains employed in the zone assay.
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来源期刊
Letters in Organic Chemistry
Letters in Organic Chemistry 化学-有机化学
CiteScore
1.30
自引率
12.50%
发文量
135
审稿时长
7 months
期刊介绍: Aims & Scope Letters in Organic Chemistry publishes original letters (short articles), research articles, mini-reviews and thematic issues based on mini-reviews and short articles, in all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is to publish quality papers rapidly by taking full advantage of latest technology for both submission and review of the manuscripts. The journal is an essential reading for all organic chemists belonging to both academia and industry.
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