Si Xuezhen, Pan Xuze, Xue Jintang, Yao Qingxia, Huang Xianqiang, Duan Wenzeng, Qiu Yi, Su Jie, Cao Minglei, Li Jun
School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory/Collaborative Innovation Center of Chemical Energy Storage and Novel Cell TechnologyLiaocheng University Liaocheng 252000 China
College of Chemistry and Molecular Engineering, Peking University Beijing 100871 PR China
RSC Adv. 2022 Nov 23;12(52):33501-33509. doi: 10.1039/d2ra06545b. eCollection 2022 Nov 22.
A family of microporous and robust Ln(iii)-based metal-organic frameworks (1-Ln, Ln = Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) have been obtained using 4,4',4''-nitrilotribenzoic acid (HNTB) in NMP-HCl solvent. Both single-crystal and powder X-ray diffraction analyses demonstrate that 1-Ln are isostructural and possess 3D frameworks with permanent porosity for Ar and CO adsorption. Strikingly, the incorporation of both Lewis acidic lanthanide ions and the basic triphenylamine group into 1-Ln makes them efficient acid-base catalysts for both cycloaddition of epoxides with CO and one-pot cascade deacetalization-Knoevenagel reactions. The systematic catalytic studies show that 1-Tb and 1-Yb possess the best catalytic activities for both reactions, indicating the catalytic activities of these Ln-MOFs are strongly dependent on metal Lewis acid sites embedded in the frameworks.
使用4,4',4''-次氮基三苯甲酸(HNTB)在NMP-HCl溶剂中获得了一系列微孔且坚固的基于Ln(iii)的金属有机框架(1-Ln,Ln = Sm、Eu、Gd、Tb、Dy、Ho、Er、Yb)。单晶和粉末X射线衍射分析均表明1-Ln具有同构结构,并拥有对Ar和CO吸附具有永久孔隙率的三维框架。引人注目的是,将路易斯酸性镧系离子和碱性三苯胺基团同时引入1-Ln中,使其成为用于环氧化物与CO环加成反应以及一锅法串联脱缩醛-Knoevenagel反应的高效酸碱催化剂。系统的催化研究表明,1-Tb和1-Yb对这两种反应均具有最佳催化活性,这表明这些Ln-MOFs的催化活性强烈依赖于嵌入框架中的金属路易斯酸位点。