卟啉
电化学
电极
镍
共价键
催化作用
对乙酰氨基酚
化学
无机化学
材料科学
核化学
光化学
有机化学
物理化学
生物化学
作者
Lu Hou,Yue Jiang,Lizhen Chen,Shengfeng Zhang,Heng-Ye Li,Mei‐Jie Wei,Fen‐Ying Kong,Wei Wang
出处
期刊:Analytical Methods
[Royal Society of Chemistry]
日期:2024-01-01
卷期号:16 (45): 7789-7794
被引量:6
摘要
Covalent organic frameworks (COFs) can be rationally designed with functional organic ligands to improve the electrochemical responsiveness of the electrode toward certain medicinal compounds. In this study, we synthesized a COF-Ni electrocatalyst material, which is formed by covalent coupling of electron-rich 2,3,6,7-tetrakis (4-formylphenyl) tetrakis (4-imidazolyl) (TTF-4CHO) and hole-rich 5,10,15,20-tetrakis (4-aminophenyl) porphyrin nickel(II) (TAPP-Ni). The reasonable electron transfer path design, the large specific surface area of the COF and the physical properties of ordered nanopores, as well as the Ni-N4 bond as a highly active catalytic center, allow the COF-Ni material modified electrode to exhibit excellent sensing performance for acetaminophen (ACOP). The detection limit for ACOP is as low as 47.6 nM, with a linear range of 1-1500 μM, which is better than for most of the reported sensors. With superior interference resistance and good stability performance, COF-Ni is a highly suited electrode modification material for real-world sample detection, which provided a new perspective for application of COF materials in drug analysis.
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