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揭示共价键合碳基质对铁氮活性位点的调控以增强类漆酶活性:用于酚类污染物的先进检测与降解

Unraveling the modulation of covalently bonded carbon matrix on Fe-N active sites for enhanced laccase-like activity: toward advanced detection and degradation of phenolic pollutants.

作者信息

Zhang Guo-Qi, Long Xia, Shi Yu-Han, Wu Wei, Zhou Xin-Yue, Jiang Wen-Cai, Li Tian-Qi, Xiang Wen-Jing, Liu Wei-Ping, Zhao Yan

机构信息

Department of Chemistry, School of Science, Xihua University, Chengdu, 610039, People's Republic of China.

Department of Transfusion Medicine, Zigong First People's Hospital, Zigong, 643000, People's Republic of China.

出版信息

Mikrochim Acta. 2025 Jun 28;192(7):464. doi: 10.1007/s00604-025-07314-7.

Abstract

Herein, we present a proof-of-concept investigation into the assessment of the laccase-like activity of covalently bonded carbon environments connected to Fe-N sites, using the closed π conjugated phthalocyanine-based intrinsic covalent organic polymers (COP) with well-designed structures. Based on the theoretical prediction and experimental implementation, the impact of the covalent-bonded carbon matrix on the laccase-like activity of COP-X (X represents the degree of conjugation) was systematically investigated. Further calculation results by density functional theory showed that the strongest laccase-like catalytic activity of COP-2 may be due to the facile desorption of catalytic intermediates, and the laccase-like catalytic mechanism of COP-2 nanozymes was also deeply understood. As anticipated, the utilization of COP-2 nanozymes with laccase-like activity enabled the achievement of excellent sensitivity for monitoring epinephrine in human serum. In addition, the COP-2 nanozymes also facilitate the detection and degradation of phenolic pollutants present in the environment. This finding presents a novel perspective for the rational design of high-performance laccase-like iron based nanozymes, and also lays the foundation for clarifying the origin of the laccase-like activity of nanozymes.

摘要

在此,我们展示了一项概念验证研究,该研究利用具有精心设计结构的基于封闭π共轭酞菁的本征共价有机聚合物(COP),对连接到Fe-N位点的共价键合碳环境的漆酶样活性进行评估。基于理论预测和实验实施,系统地研究了共价键合碳基质对COP-X(X代表共轭程度)的漆酶样活性的影响。密度泛函理论的进一步计算结果表明,COP-2最强的漆酶样催化活性可能归因于催化中间体的易于解吸,并且对COP-2纳米酶的漆酶样催化机制也有了深入了解。正如预期的那样,利用具有漆酶样活性的COP-2纳米酶能够实现对人血清中肾上腺素监测的优异灵敏度。此外,COP-2纳米酶还促进了环境中存在的酚类污染物的检测和降解。这一发现为高性能漆酶样铁基纳米酶的合理设计提供了新的视角,也为阐明纳米酶漆酶样活性的起源奠定了基础。

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