School of Chemistry and SFI AMBER Centre, Trinity College Dublin, College Green, Dublin 2, Ireland.
Dalton Trans. 2019 Nov 7;48(41):15487-15492. doi: 10.1039/c9dt02117e. Epub 2019 Jul 10.
A porous Zr-based MOF, [Zr(BTEB)(μ-O)(μ-OH)(HO)], which contains partially hydrated, 12-connected {Zr} nodes and extended carboxylate ligands (BTEB), was synthesized and physicochemically characterised. The resulting (12,3)-connected, 3D framework adopts an uncommon llj topology with a large, solvent accessible void volume of ca. 79% of the unit cell volume. The porous structure facilitates the uptake of N and activated samples give rise to BET surface areas of >1000 m g. Furthermore, the porosity and accessibility of Lewis acidic Zr(iv) sites promote the catalytic transformation of gaseous CO to cyclic carbonates via cycloaddition reactions using epoxide reactants, whereby solvated MOFs exhibit higher catalytic performance than thermally treated samples.
一种多孔的 Zr 基 MOF,[Zr(BTEB)(μ-O)(μ-OH)(HO)],它含有部分水合的 12 连接的 {Zr} 节点和扩展的羧酸盐配体(BTEB),被合成并进行了物理化学性质的表征。所得的(12,3)连接的 3D 骨架采用了不常见的 llj 拓扑结构,具有约 79%的单位晶胞体积的大的、可溶剂进入的空隙体积。多孔结构有利于 N 的吸收,并且经过活化后,BET 表面积大于 1000 m²/g。此外,Lewis 酸性 Zr(iv)位的多孔性和可及性促进了通过环加成反应使用环氧化物反应物将气态 CO 转化为环状碳酸酯,其中溶剂化的 MOF 表现出比热处理样品更高的催化性能。