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一种基于深共晶溶剂胶束中酸铜纳米簇的新型“关闭”荧光分析方法用于共聚集诱导荧光增强及其应用。

A novel"turn-off"fluorescence assay based on acid-copper nanoclusters in deep eutectic solvent micelles for co-aggregation inducing fluorescence enhancement and its application.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, PR China; College of Material and Chemical Engineering, Tongren University, Tongren, 554300, PR China.

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, PR China.

出版信息

Talanta. 2021 Feb 1;223(Pt 1):121731. doi: 10.1016/j.talanta.2020.121731. Epub 2020 Oct 6.

Abstract

As mixtures, deep eutectic solvent (DES) is designability. By adjusting the long alkyl chain hydrogen bond acceptors (HBAs) or hydrogen bond donors (HBDs), the DES displays surfactant characteristics and can form micelles. Hence, a novel, simple, facile and green natural organic acids capped copper nanoclusters (Aci-CuNCs) was synthesized and the spectrum behavior of Aci-CuNCs in DES micelles was researched. It was found that the surfactant-like DES can form micellar co-aggregation with Aci-CuNCs, resulting in the fluorescence (FL) intensive of Aci-CuNCs increase. Corresponding performance of spectral properties of Aci-CuNCs in DES medium were systematically studied by fourier transform infrared spectrometer, 3D FL spectroscopy, FL emission/excitation spectra, ultraviolet absorption spectroscopy. In the mechanism exploration part, on the one hand, the existence of micellar co-aggregation was confirmed by the conductivity, the mass effect of DES, dynamic light scattering and transmission electron microscopy. On the other hand, the influence of different kinds of DESs (types of HBAs/HBDs, molar ratio) and some possible factors (ionic strength and temperature) were discussed in detail to investigate the main driving forces for the formation of micellar co-aggregates. The results of mechanism exploration prove that the long alkyl chain of DES is amphiphilic which can form micellar co-aggregation with Aci-CuNCs through hydrogen bonding. The DES micelle provides Aci-CuNCs with a relatively stable and closed micro-environment which can effectively prevent collisions with water molecules and weakening of fluorescence intensity. On the basic of the above research, a "turn-off" fluorimetric method based on Aci-CuNCs in DES medium was applied for the determination of Fe. Under the optimum conditions, the assay worked in the Fe concentration ranges from 1 to -20 μM and had a detection limit of 0.0374 μM. Method validation study illustrates the proposed system can provide a good accuracy, repeatability and stability conditions. Furthermore, the real sample analysis result demonstrates that no obvious matrix effect is found. As a consequence, the FL assays (Aci-CuNCs-based DES) composed of natural organic acid capped CuNCs and green solvent DES provides a simple, gentle and environmentally friendly method for the detection of iron ions.

摘要

作为混合物,深共晶溶剂(DES)是可设计的。通过调整长链烷基氢键供体(HBDs)或氢键受体(HBAs),DES 显示出表面活性剂的特性,并能形成胶束。因此,合成了一种新型、简单、方便和绿色的天然有机酸封端铜纳米簇(Aci-CuNCs),并研究了 Aci-CuNCs 在 DES 胶束中的光谱行为。结果表明,具有表面活性剂性质的 DES 可以与 Aci-CuNCs 形成胶束共聚集,从而导致 Aci-CuNCs 的荧光(FL)强度增加。通过傅里叶变换红外光谱仪、3D FL 光谱仪、FL 发射/激发光谱仪、紫外吸收光谱仪系统地研究了 Aci-CuNCs 在 DES 介质中的光谱性质。在机制探索部分,一方面,通过电导率、DES 的质量效应、动态光散射和透射电子显微镜证实了胶束共聚集的存在。另一方面,详细讨论了不同类型的 DES(HBAs/HBDs 的类型、摩尔比)和一些可能的因素(离子强度和温度)对胶束共聚集形成的影响,以研究形成胶束共聚集的主要驱动力。机制探索的结果证明,DES 的长烷基链具有两亲性,可以通过氢键与 Aci-CuNCs 形成胶束共聚集。DES 胶束为 Aci-CuNCs 提供了一个相对稳定和封闭的微环境,有效地防止了与水分子的碰撞和荧光强度的减弱。在上述研究的基础上,建立了基于 DES 中 Aci-CuNCs 的“关闭”荧光测定铁的方法。在最佳条件下,该测定方法在 1 至 -20 μM 的铁浓度范围内工作,检测限为 0.0374 μM。方法验证研究表明,该体系具有良好的准确性、重复性和稳定性。此外,实际样品分析结果表明,没有明显的基质效应。因此,由天然有机酸封端的 CuNCs 和绿色溶剂 DES 组成的 FL 测定(基于 Aci-CuNCs 的 DES)为铁离子的检测提供了一种简单、温和、环保的方法。

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