用于选择性检测 Zn2+、Al3+ 和 F- 离子的基于水杨醛的双响应 "开启 "荧光化学传感器:理论研究以及在斑马鱼幼体活细胞成像和分子逻辑门操作中的应用。

Abbas Khaja Raees Ahmed, Ramalingam Gajendhiran, Sivaraj Mithra, Seepoo Abdul Majeed, Azeez Sait Sahul Hameed, Rajakkani Paulpandiyan, Subbaiah Maniyammai, Gurusamy Thangavelu Senthil Andavan, MohamedHanifa NizamMohideen, Aziz Kalilur Rahiman
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引用次数: 0

摘要

四种基于水杨醛的双响应化学传感器 1,5-双(5-溴水杨醛)腙(R1)、1,5-双(5-溴水杨醛)硫代腙(R2)、合成并鉴定了 1,5-双(3-乙氧基水杨醛)腙(R3)和 1,5-双(3-乙氧基水杨醛)硫代腙(R4)。通过单晶 X 射线衍射技术确认了 R1 和 R3 的分子结构,它们分别在正方晶 Pbcn 和单斜晶 P21/n 空间群中结晶。通过比色法、吸收光谱法、荧光光谱法、1H NMR 光谱法和理论研究,考察了化学传感器分子对所选阳离子(K+、Ca2+、Mn2+、Co2+、Ni2+、Cu2+、Zn2+、Fe3+ 和 Al3+)和阴离子(F-、Cl-、Br-、I-、HSO4-、H2PO4-、ClO4-、N3- 和 NO3-)的识别特性。传感器分子对 Co2+、Ni2+、Cu2+ 和 Fe3+ 阳离子以及 F- 阴离子显示出比色反应。有趣的是,Zn2+ 和 Al3+ 阳离子只显示出 "开启 "荧光反应,而 F- 阴离子则同时显示出比色和荧光反应。利用荧光滴定法得出的贝尼尼-希尔德布兰德(B-H)方程确定了结合常数,发现 R3 与 Al3+ 阳离子的结合常数较高(2.03 × 106 M-1),检出限较低(1.79 μM);R4 与 F- 阴离子的结合常数较低(5.13 × 105 M-1),检出限较低(5.23 μM)。化学传感器建立了 1 : 2 和 1 :约伯图证实,化学传感器分别与被感应的阳离子和阴离子建立了 1 : 2 和 1 : 1 的结合比例关系。计算研究表明,与自由化学传感器相比,当化学传感器与被感应的无机离子结合时,其 HOMO-LUMO 带隙较低。此外,观察到的 Zn2+ 和 Al3+ 阳离子的荧光行为促使我们研究其在斑马鱼幼体活细胞成像以及分子逻辑门开发中的实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Salicylidene-based dual-responsive 'turn on' fluorometric chemosensors for the selective detection of Zn2+, Al3+ and F- ions: theoretical investigation and applications in the live cell imaging of zebrafish larvae and molecular logic gate operation.

Four salicylidene-based dual-responsive chemosensors 1,5-bis(5-bromosalicylaldehyde)carbohydrazone (R1), 1,5-bis(5-bromosalicylaldehyde)thiocarbohydrazone (R2), 1,5-bis(3-ethoxysalicylaldehyde)carbohydrazone (R3) and 1,5-bis(3-ethoxysalicylaldehyde)thiocarbohydrazone (R4) were synthesized and characterized. The molecular structures of R1 and R3 were confirmed by single crystal X-ray diffraction technique, which crystallized in the orthorhombic Pbcn and monoclinic P21/n space groups, respectively. The chemosensor molecules were investigated for their recognition properties against the selected cations (K+, Ca2+, Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Fe3+ and Al3+) and anions (F-, Cl-, Br-, I-, HSO4-, H2PO4-, ClO4-, N3- and NO3-) by colorimetry, absorption spectroscopy, fluorescence spectroscopy, 1H NMR spectroscopy and theoretical studies. The sensor molecules showed colorimetric responses for the Co2+, Ni2+, Cu2+ and Fe3+ cations and the F- anion. Interestingly, the Zn2+ and Al3+ cations showed only the 'turn on' fluorometric response, whereas the F- anion showed both colorimetric and fluorometric responses. The binding constants were determined using the Benesi-Hildebrand (B-H) equation from the fluorescence titrations and found to be higher for R3 towards the Al3+ cation (2.03 × 106 M-1) with a low limit of detection (1.79 μM) and for R4 towards the F- anion (5.13 × 105 M-1) with a low limit of detection (5.23 μM). The chemosensors established 1 : 2 and 1 : 1 binding stoichiometries with the sensed cations and anion, respectively, as confirmed by Job's plots. The computational studies show a lower band gap of HOMO-LUMO when the chemosensors bind with the sensed inorganic ions compared to the free chemosensors. Furthermore, the observed fluorescent behaviour of the Zn2+ and Al3+ cations have motivated us to investigate the practical applications in the live cell-imaging of zebrafish larvae as well as in the development of a molecular logic gate.

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来源期刊
Journal of materials chemistry. B
Journal of materials chemistry. B 化学科学, 工程与材料, 生命科学, 分析化学, 高分子组装与超分子结构, 高分子科学, 免疫生物学, 免疫学, 生化分析及生物传感, 组织工程学, 生物力学与组织工程学, 资源循环科学, 冶金与矿业, 生物医用高分子材料, 有机高分子材料, 金属材料的制备科学与跨学科应用基础, 金属材料, 样品前处理方法与技术, 有机分子功能材料化学, 有机化学
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