碳酸酐酶
咪唑酯
沸石咪唑盐骨架
化学
表面改性
催化作用
水解
金属有机骨架
组合化学
生物催化
活动站点
协同催化
酶
有机化学
反应机理
物理化学
吸附
作者
Fanchen Meng,Cheng Xu,Linghai Zhang,Xiaohan Huang,Xinglong Zhang,Wenlei Zhang,Yongqi Luo,Weina Zhang,Wei Huang,Fengwei Huo,Weina Zhang
出处
期刊:Research
[American Association for the Advancement of Science]
日期:2024-01-01
卷期号:7
标识
DOI:10.34133/research.0434
摘要
Metal-organic frameworks (MOFs) have been widely considered as ideal platforms for the preparation of biomimetic catalysts, but it remains challenging to fabricate MOF-based enzyme-like catalysts with optimal activity. Here, we leverage the inherent flexibility of MOFs and propose a novel trans-functionalization strategy to construct a carbonic anhydrase (CA) mimic by the structural transformation from ZIF-L to ZIF-8. Theoretical and experimental results reveal that during the structural transformation, the hydroxyl group will preferentially coordinate with the interlayer Zn clusters to form the CA-like active center Zn-N 3 -OH. Therefore, more accessible active centers are generated on the as-prepared ZIF-8-OH, resulting in substantially enhanced catalytic activity in the hydrolysis of para -nitrophenyl acetate.
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