化学
对苯二甲酸
酰胺
选择性
配体(生物化学)
羧酸盐
组合化学
化学稳定性
催化作用
溶剂热合成
无机化学
立体化学
有机化学
聚酯纤维
生物化学
受体
作者
Yu‐Ke Lu,Haihua Wang,Qixuan Hu,Yao-Yu Ma,Lei Hou,Yao‐Yu Wang
标识
DOI:10.1016/j.jssc.2020.121890
摘要
By employing the ligand 2-(isonicotinamido)terephthalic acid (H2L) containing the amide functional groups, a Cd-MOF, {[Cd2L2(H2O)2]·4H2O}n (1) has been constructed by solvothermal synthesis. The dinuclear clusters [Cd2(COO)2] in 1 are linked by the pyridinyl and carboxylate groups of ligands to form a three-dimensional (3D) skeleton, containing 1D channels with the free amide groups. The activated framework shows good stability in water and high selectivity for CO2 over CH4. The open Cd2+ site as Lewis acidic center makes the MOF achieve efficiently catalytic conversion for CO2 cycloaddition with epoxides. Furthermore, 1 also exhibits good chemical stability in water, allowing the detection for ronidazole (RDZ) and dimetridazole (DTZ) with the low detection limit and rapid response.
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