烷基
催化作用
材料科学
薗头偶联反应
表面能
金属有机骨架
自组装
配体(生物化学)
化学工程
金属
钯
吸附
高分子化学
复合材料
纳米技术
化学
有机化学
工程类
受体
冶金
生物化学
作者
Neng‐Xiu Zhu,Zhang‐Wen Wei,Cheng‐Xia Chen,Dawei Wang,Chen‐Chen Cao,Qian‐Feng Qiu,Ji‐Jun Jiang,Hai‐Ping Wang,Cheng‐Yong Su
标识
DOI:10.1002/anie.201909912
摘要
Abstract We transformed the hydrophilic metal–organic framework (MOF) UiO‐67 into hydrophobic UiO‐67‐R s (R=alkyl) by introducing alkyl chains into organic linkers, which not only protected hydrophilic Zr 6 O 8 clusters to make the MOF interspace superoleophilic, but also led to a rough crystal surface beneficial for superhydrophobicity. The UiO‐67‐R s displayed high acid, base, and water stability, and long alkyl chains offered better hydrophobicity. Good hydrophobicity/oleophilicity were also possible with mixed‐ligand MOFs containing metal‐binding ligands. Thus, a (super)hydrophobic MOF catalyst loaded with Pd centers efficiently catalyzed Sonogashira reactions in water at ambient temperature. Studies of the hydrophobic effects of the coordination interspace and the outer surface suggest a simple de novo strategy for the synthesis of superhydrophobic MOFs that combine surface roughness and low surface energy. Such MOFs have potential for environmentally friendly catalysis and water purification.
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