Lee Jaechul, Chuah Chong Yang, Kim Jaheon, Kim Youngsuk, Ko Nakeun, Seo Younggyu, Kim Kimoon, Bae Tae Hyun, Lee Eunsung
Center for Self-assembly and Complexity, Institute for Basic Science (IBS), Pohang, 37673, Republic of Korea.
Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Angew Chem Int Ed Engl. 2018 Jun 25;57(26):7869-7873. doi: 10.1002/anie.201804442. Epub 2018 May 16.
Separation of acetylene from carbon dioxide and ethylene is challenging in view of their similar sizes and physical properties. Metal-organic frameworks (MOFs) in general are strong candidates for these separations owing to the presence of functional pore surfaces that can selectively capture a specific target molecule. Here, we report a novel 3D microporous cationic framework named JCM-1. This structure possesses imidazolium functional groups on the pore surfaces and pyrazolate as a metal binding group, which is well known to form strong metal-to-ligand bonds. The selective sorption of acetylene over carbon dioxide and ethylene in JCM-1 was successfully demonstrated by equilibrium gas adsorption analysis as well as dynamic breakthrough measurement. Furthermore, its excellent hydrolytic stability makes the separation processes highly recyclable without a substantial loss in acetylene uptake capacity.
鉴于乙炔与二氧化碳和乙烯的分子尺寸和物理性质相似,将它们分离具有挑战性。由于金属有机框架(MOF)存在功能性孔表面,能够选择性地捕获特定目标分子,因此总体上是这些分离的有力候选材料。在此,我们报道了一种名为JCM-1的新型三维微孔阳离子框架。该结构在孔表面具有咪唑鎓官能团,以吡唑盐作为金属结合基团,众所周知,它能形成强的金属-配体键。通过平衡气体吸附分析以及动态穿透测量,成功证明了JCM-1对乙炔相对于二氧化碳和乙烯的选择性吸附。此外,其优异的水解稳定性使得分离过程具有高度可回收性,且乙炔吸附容量不会有实质性损失。