Boosting CO 2 chemical fixation over MOF-808 by the introduction of functional groups and defective Zr sites

CO cycloaddition has emerged as a promising approach for producing value-added cyclocarbonates and mitigating greenhouse gas emissions. Although MOF-808 serves as a stable catalyst for cycloaddition, its limited activity constrains broader applications. Through the modification with a fluoride group...

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Bibliographic Details
Published inChemical communications (Cambridge, England) Vol. 60; no. 23; pp. 3170 - 3173
Main Authors Zhou, Minghui, Qu, Zhengyan, Zhang, Jiuxuan, Jiang, Hong, Tang, Zhenchen, Chen, Rizhi
Format Journal Article
LanguageEnglish
Published England 14.03.2024
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Summary:CO cycloaddition has emerged as a promising approach for producing value-added cyclocarbonates and mitigating greenhouse gas emissions. Although MOF-808 serves as a stable catalyst for cycloaddition, its limited activity constrains broader applications. Through the modification with a fluoride group a ligand exchange method, F-MOF-808-1.5 exhibits exceptional performance, achieving a 98.8% conversion with 97.8% selectivity to epichlorohydrin carbonate-marking a substantial 100% improvement compared to pristine MOF-808. The defective Zr sites and the electron-withdrawing groups synergistically promote the ring opening of epoxides. Furthermore, the catalyst demonstrates high stability over multiple reaction cycles. Notably, without adding solvents and co-catalysts, F-MOF-808-1.5 outperforms most reported MOF-based catalysts.
ISSN:1359-7345
1364-548X
DOI:10.1039/D3CC06154J