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Axial Chlorination Engineering of Single-Atom Nanozyme: Fe‑N4Cl Catalytic Sites for Efficient Peroxidase-Mimicking

Developing axial coordination engineering of single-atom nanozymes (SAzymes), directly regulating the axial coordination environment of the catalytic site, and optimizing the axial adsorption are meaningful and challenging for boosting the enzyme-like activities. Herein, the axial chlorination engin...

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Bibliographic Details
Published in:Journal of the American Chemical Society 2024-12, Vol.146 (48), p.33239-33248
Main Authors: Wei, Shengjie, Sun, Minmin, Huang, Juan, Chen, Zhengbo, Wang, Xijun, Gao, Lizeng, Zhang, Jijie
Format: Article
Language:English
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Summary:Developing axial coordination engineering of single-atom nanozymes (SAzymes), directly regulating the axial coordination environment of the catalytic site, and optimizing the axial adsorption are meaningful and challenging for boosting the enzyme-like activities. Herein, the axial chlorination engineering of SAzyme with the Fe-N4Cl catalytic site (Fe-N4Cl/CNCl) was first proposed, exhibiting superior peroxidase-like activity compared to the traditional Fe-N4/CN SAzyme with Fe-N4 site. The maximal reaction velocity (4.73 × 10–5 M min–1), the catalytic constant (246.4 min–1), and the specific activity (81 U/mg) catalyzed by the Fe-N4Cl/CNCl SAzyme were 4.9 times, 3.9 times, and 2.7 times those of the Fe-N4/CN SAzyme, revealing the enormous advantages of axial chlorination engineering of SAzymes for remarkably improving enzyme-like activities. Moreover, the Fe-N4Cl/CNCl SAzyme also exhibited an enhanced inhibition effect of tumor cell growth in vitro and in vivo. The density functional theory calculation revealed that the Fe-N4Cl site was more favorable for releasing •OH radical, lowering the energy barrier of rate-determining step, and accelerating the reaction rate compared to the Fe-N4 site. This work demonstrated the outstanding potential of axial chlorination engineering of SAzymes for improving enzyme-like activities and practical application in tumor therapy.
ISSN:0002-7863
1520-5126
1520-5126
DOI:10.1021/jacs.4c13335