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调节非环状菲席夫碱中的金属离子亲和力:乙烯和亚苯基连接基的比较研究。

Tuning metal ion affinity in acyclic phenanthrene schiff bases: comparative study of ethylene and phenylene linkers.

作者信息

C Haritha, M Swathi, Swamy P Chinna Ayya

机构信息

Main Group Organometallics Optoelectronic Materials and Catalysis Lab, Department of Chemistry, National Institute of Technology Calicut-673601 India

出版信息

RSC Adv. 2025 Aug 11;15(35):28481-28491. doi: 10.1039/d5ra03617h.

Abstract

We have successfully designed and synthesized two structurally simple salen-type Schiff base probes, designated as SB-1 and SB-2, for the selective detection of biologically and environmentally relevant metal ions. Fluorescence studies revealed that SB-1 exhibits a distinct "turn-on" fluorescence response in the presence of Zn, Mg, Na, and K ions, while SB-2 demonstrated a selective fluorescence enhancement exclusively for Zn ions. In addition to its fluorescence response, SB-1 displayed distinct colorimetric changes upon interaction with Zn, Cu, Mg, Na, and K ions, highlighting its broad-spectrum sensing capability. In contrast, SB-2 exhibited selective colorimetric responses only toward Zn and Cu ions. These results underscore the dual-mode sensing potential of the probes, with SB-1 offering broader ion recognition and SB-2 demonstrating higher selectivity. To gain insights into the interaction mechanism and validate the spectral changes observed experimentally, density functional theory (DFT) calculations were performed. The computational results supported the experimental findings, confirming significant electronic transitions associated with metal ion binding and providing a detailed understanding of the coordination environment and binding modes of SB-1 and SB-2 with various metal ions. H NMR titration studies further substantiated these results by revealing that the metal ions coordinate with the imine (C[double bond, length as m-dash]N) moiety at the core of the Schiff base structure, consistent with the UV-visible absorption and fluorescence spectroscopy data. The binding stoichiometry between the probes and metal ions (Zn, Cu, Mg, Na, and K) was determined to be 1 : 1, as confirmed through Job's plot analysis and supported by UV-Vis, fluorescence, DFT, and H NMR (for Zn) studies. The binding affinities were quantified using the Benesi-Hildebrand method, with association constants ( ) found to be in the range of 0.88-2.28 × 10 M. The limit of detection (LOD) for each metal ion was calculated to be in the micromolar (μM) range (0.1 to 0.05 μM), demonstrating the high sensitivity of the probes for practical sensing applications.

摘要

我们成功设计并合成了两种结构简单的席夫碱型荧光探针,命名为SB - 1和SB - 2,用于选择性检测与生物和环境相关的金属离子。荧光研究表明,SB - 1在锌、镁、钠和钾离子存在下表现出明显的“开启”荧光响应,而SB - 2仅对锌离子表现出选择性荧光增强。除了荧光响应外,SB - 1与锌、铜、镁、钠和钾离子相互作用时还表现出明显的比色变化,突出了其广谱传感能力。相比之下,SB - 2仅对锌和铜离子表现出选择性比色响应。这些结果强调了探针的双模式传感潜力,SB - 1具有更广泛的离子识别能力,而SB - 2具有更高的选择性。为了深入了解相互作用机制并验证实验观察到的光谱变化,进行了密度泛函理论(DFT)计算。计算结果支持了实验结果,证实了与金属离子结合相关的显著电子跃迁,并详细了解了SB - 1和SB - 2与各种金属离子的配位环境和结合模式。¹H NMR滴定研究进一步证实了这些结果,表明金属离子与席夫碱结构核心的亚胺(C═N)部分配位,这与紫外可见吸收和荧光光谱数据一致。通过Job曲线分析确定探针与金属离子(锌、铜、镁、钠和钾)之间的结合化学计量比为1∶1,紫外可见光谱、荧光光谱、DFT和¹H NMR(针对锌)研究也支持这一结果。使用Benesi - Hildebrand方法对结合亲和力进行了量化,缔合常数( )在0.88 - 2.28×10⁵ M范围内。计算得出每种金属离子的检测限(LOD)在微摩尔(μM)范围内(0.1至0.05 μM),表明这些探针在实际传感应用中具有高灵敏度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca4/12377188/e5c5d19d4bbf/d5ra03617h-s1.jpg

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