材料科学
连接器
金属有机骨架
亚胺
共价键
苯乙炔
共价有机骨架
组合化学
氧气储存
纳米技术
多孔性
化学工程
氧气
有机化学
化学
催化作用
计算机科学
工程类
吸附
复合材料
操作系统
作者
Jiafei Lyu,Xuan Zhang,Zhijie Chen,Ryther Anderson,Xingjie Wang,Megan C. Wasson,Peng Bai,Xianghai Guo,Timur İslamoğlu,Diego A. Gómez‐Gualdrón,Omar K. Farha
标识
DOI:10.1021/acsami.9b14439
摘要
The last decade has witnessed significant advances in the scale-up synthesis of metal-organic frameworks (MOFs) using commercially available and affordable organic linkers. However, the synthesis of MOFs using elongated and/or multitopic linkers to access MOFs with large pore volume and/or various topologies can often be challenging due to multistep organic syntheses involved for linker preparation. In this report, a modular MOF synthesis strategy is developed by utilizing the coordination and covalent bonds formation in one-pot strategy where monoacid-based ligands reacted to form ditopic ligands, which then assembled into a three-dimensional MOF with Zr6 clusters. Chemical stability of the resulting materials was significantly enhanced through converting the imine bond into robust linkage via cycloaddition with phenylacetylene. Oxygen storage capacities of the MOFs were measured, and enhanced volumetric O2 uptake was observed for the stabilized MOF, NU-401-Q.
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