化学
亲核细胞
碳酸酐酶
金属有机骨架
金属
密度泛函理论
配体(生物化学)
碳酸酐酶Ⅱ
无机化学
氢键
微量金属
锌
物理化学
分子
计算化学
有机化学
催化作用
吸附
酶
受体
生物化学
作者
Caitlin E. Bien,Kai K. Chen,Szu‐Chia Chien,Benjamin R. Reiner,Li‐Chiang Lin,Casey R. Wade,W.S. Winston Ho
摘要
A Zn benzotriazolate metal–organic framework (MOF), [Zn(ZnO2CCH3)4(bibta)3] (1, bibta2– = 5,5′-bibenzotriazolate), has been subjected to a mild CH3CO2–/HCO3– ligand exchange procedure followed by thermal activation to generate nucleophilic Zn–OH groups that resemble the active site of α-carbonic anhydrase. The postsynthetically modified MOF, [Zn(ZnOH)4(bibta)3] (2*), exhibits excellent performance for trace CO2 capture and can be regenerated at mild temperatures. IR spectroscopic data and density functional theory (DFT) calculations reveal that intercluster hydrogen bonding interactions augment a Zn–OH/Zn–O2COH fixation mechanism.
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