https://scholars.lib.ntu.edu.tw/handle/123456789/611479
標題: | Bioinspired Metal-Organic Framework for Trace CO2 Capture | 作者: | Bien C.E. Chen K.K. Chien S.-C. Reiner B.R. Lin L.-C. Wade C.R. Ho W.S.W. LI-CHIANG LIN |
關鍵字: | Carbon dioxide;Carbonic anhydrase;Crystalline materials;Density functional theory;Hydrogen bonds;Organometallics;Trace elements;Alpha-carbonic anhydrase;Fixation mechanisms;Hydrogen bonding interactions;Ligand exchanges;Metal organic framework;Mild temperatures;Spectroscopic data;Thermal activation;Zinc compounds;benzotriazole;biomimetic material;carbon dioxide;carbonate dehydratase;metal organic framework;triazole derivative;zinc;chemistry;enzyme active site;hydrogen bond;isolation and purification;molecular model;synthesis;Biomimetic Materials;Carbon Dioxide;Carbonic Anhydrases;Catalytic Domain;Hydrogen Bonding;Metal-Organic Frameworks;Models, Molecular;Triazoles;Zinc | 公開日期: | 2018 | 卷: | 140 | 期: | 40 | 起(迄)頁: | 12662-12666 | 來源出版物: | Journal of the American Chemical Society | 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. Copyright ? 2018 American Chemical Society. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054344948&doi=10.1021%2fjacs.8b06109&partnerID=40&md5=7837b4a56db02e3654d6b6697893a75d https://scholars.lib.ntu.edu.tw/handle/123456789/611479 |
DOI: | 10.1021/jacs.8b06109 |
顯示於: | 化學工程學系 |
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