Fluorescent probe for Fe3+ detection based on a guest molecular luminescent metal–organic framework

IF 1 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
Lei Yang, Tangxuan Xu, Chenghao Li, Yuezhu Yang, Jing Huang
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引用次数: 0

Abstract

The zinc(II) bis-(8-hydroxyquinoline) (Znq2) has excellent photoluminescence properties, and its fluorescence emission can be significantly quenched by Fe3+ in water. To accelerate the detection response of Znq2 to Fe3+, a luminescent metal–organic framework Znq2@ZIF-8 based on guest molecular luminescence was constructed by growing zeolite imidazolate framework-8 (ZIF-8) on the outer surface of Znq2. The results show that the prepared Znq2@ZIF-8 has an octahedral core–shell structure, a particle size of approximately 1–3 μm, an enhanced specific surface area of 1105.41 m2 g−1, and with a stable green luminescence at 495 nm. A fluorescence analytical method was developed for the detection of Fe3+ in water, the correlation coefficients were significant in the Fe3+ concentration range of 0–600 μmol L−1, and the limit of detection was as low as 3.89 μmol L−1. The spiked recoveries of tap water samples demonstrated that the method could be applied to practical applications. The mechanism of fluorescence detection is that Fe3+ participates in the competitive coordination of Znq2@ZIF-8 metal centers, leading to the collapse of the crystal structure, meanwhile, Fe3+ produces a certain degree of competitive absorption of the excitation light of Znq2@ZIF-8. This method was applied for the detection of Fe3+ in water with good selectivity, anti-interference ability, and has the potential to be used as a rapid detection method.
基于客体分子发光金属有机框架的 Fe3+ 检测荧光探针
双(8-羟基喹啉)锌(II)(Znq2)具有优异的光致发光特性,其荧光发射可被水中的Fe3+显著淬灭。为了加速 Znq2 对 Fe3+ 的检测响应,研究人员在 Znq2 外表面生长沸石咪唑啉框架-8(ZIF-8),构建了基于客体分子发光的发光金属有机框架 Znq2@ZIF-8。结果表明,所制备的 Znq2@ZIF-8 具有八面体核壳结构,粒径约为 1-3 μm,比表面积增强至 1105.41 m2 g-1,并在 495 nm 波长处具有稳定的绿色发光。所建立的荧光分析方法可用于检测水中的 Fe3+,在 Fe3+浓度为 0-600 μmol L-1 的范围内相关系数显著,检出限低至 3.89 μmol L-1。自来水样品的加标回收率表明该方法可用于实际应用。荧光检测的机理是Fe3+参与了Znq2@ZIF-8金属中心的竞争配位,导致晶体结构塌缩,同时Fe3+对Znq2@ZIF-8的激发光产生一定程度的竞争吸收。该方法应用于水中Fe3+的检测,具有良好的选择性和抗干扰能力,有望作为一种快速检测方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemical Research
Journal of Chemical Research CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
2.30
自引率
0.00%
发文量
66
审稿时长
1.0 months
期刊介绍: The Journal of Chemical Research is a monthly journal which has a broad international authorship and publishes research papers and reviews in all branches of experimental chemistry. Established in 1977 as a joint venture by the British, French and German chemical societies it maintains the high standards set by the founding societies. Each paper is independently peer reviewed and only carefully evaluated contributions are accepted. Recent papers have described new synthetic methods, new heterocyclic compounds, new natural products, and the inorganic chemistry of metal complexes.
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