Leda Amanda, Hassani Mina, Rebis Tomasz, Falkowski Michal, Piskorz Jaroslaw, Mlynarczyk Dariusz T, McNeice Peter, Milczarek Grzegorz
Institute of Chemistry and Technical Electrochemistry, Faculty of Chemical Technology, Poznan University of Technology, Berdychowo 4, 60-965 Poznan, Poland.
Department of Medicinal Chemistry, Collegium Medicum in Bydgoszcz, Faculty of Pharmacy, Nicolaus Copernicus University in Torun, Dr. A. Jurasza 2, 85-089 Bydgoszcz, Poland.
Nanomaterials (Basel). 2023 Feb 25;13(5):862. doi: 10.3390/nano13050862.
A metal-free porphyrazine derivative with peripheral phthalimide substituents was metallated with a nickel(II) ion. The purity of the nickel macrocycle was confirmed using HPLC, and characterized by MS, UV-VIS, and 1D (H, C) and 2D (H-C HSQC, H-C HMBC, H-H COSY) NMR techniques. The novel porphyrazine was combined with various carbon nanomaterials, such as carbon nanotubes-single walled (SWCNTs) and multi-walled (MWCNTs), and electrochemically reduced graphene oxide (rGO), to create hybrid electroactive electrode materials. The carbon nanomaterials' effect on the electrocatalytic properties of nickel(II) cations was compared. As a result, an extensive electrochemical characterization of the synthesized metallated porphyrazine derivative on various carbon nanostructures was carried out using cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). An electrode modified with carbon nanomaterials GC/MWCNTs, GC/SWCNTs, or GC/rGO, respectively, was shown to have a lower overpotential than a bare glassy carbon electrode (GC), allowing for the measurement of hydrogen peroxide in neutral conditions (pH 7.4). It was shown that among the tested carbon nanomaterials, the modified electrode GC/MWCNTs/ exhibited the best electrocatalytic properties in the direction of hydrogen peroxide oxidation/reduction. The prepared sensor was determined to enable a linear response to HO in concentrations ranging between 20-1200 µM with the detection limit of 18.57 µM and sensitivity of 14.18 µA mM cm. As a result of this research, the sensors produced here may find use in biomedical and environmental applications.
一种带有周边邻苯二甲酰亚胺取代基的无金属卟吩嗪衍生物与镍(II)离子进行了金属化反应。使用高效液相色谱法(HPLC)确认了镍大环化合物的纯度,并通过质谱(MS)、紫外可见光谱(UV-VIS)以及一维(H、C)和二维(H-C HSQC、H-C HMBC、H-H COSY)核磁共振技术对其进行了表征。这种新型卟吩嗪与各种碳纳米材料相结合,如单壁碳纳米管(SWCNTs)、多壁碳纳米管(MWCNTs)和电化学还原氧化石墨烯(rGO),以制备混合电活性电极材料。比较了碳纳米材料对镍(II)阳离子电催化性能的影响。结果,使用循环伏安法(CV)、计时电流法(CA)和电化学阻抗谱(EIS)对合成的金属化卟吩嗪衍生物在各种碳纳米结构上进行了广泛的电化学表征。分别用碳纳米材料GC/MWCNTs、GC/SWCNTs或GC/rGO修饰的电极显示出比裸玻碳电极(GC)更低的过电位,从而能够在中性条件(pH 7.4)下测量过氧化氢。结果表明,在所测试的碳纳米材料中,修饰电极GC/MWCNTs在过氧化氢氧化/还原方向上表现出最佳的电催化性能。所制备的传感器在20-1200 μM浓度范围内对HO表现出线性响应,检测限为18.57 μM,灵敏度为14.18 μA mM cm。这项研究的结果表明,这里生产的传感器可能在生物医学和环境应用中找到用途。