结晶学
铀酰
连接器
八面体
网状结缔组织
多面体
三角棱镜分子几何学
拓扑(电路)
化学
金属有机骨架
平面的
铀
配体(生物化学)
配位几何学
材料科学
晶体结构
几何学
分子
计算机科学
氢键
物理化学
有机化学
计算机图形学(图像)
操作系统
生物化学
医学
受体
病理
冶金
吸附
组合数学
数学
作者
Zhijie Chen,Penghao Li,Xuan Zhang,Mohammad Rasel Mian,Xingjie Wang,Peng Li,Zhichang Liu,M. O’Keeffe,J. Fraser Stoddart,Omar K. Farha
出处
期刊:Nano Research
[Springer Nature]
日期:2020-02-28
卷期号:14 (2): 376-380
被引量:35
标识
DOI:10.1007/s12274-020-2690-3
摘要
We report that the rational reticular design of metal–organic frameworks (MOFs) from building units of known geometries is essential for enriching the diversity of MOF structures. Unexpected and intriguing structures, however, can also arise from subtle changes in the rigidity/length of organic linkers and/or synthetic conditions. Herein, we report three uranium-based MOF structures—i.e., NU-135X (X = 0, 1, 2)—synthesized from trigonal planar uranyl nodes and triptycene-based hexacarboxylate ligands with variable arm lengths. A new chiral 3,6-connected nuc net was observed in NU-1350, while the extended versions of the ligand led to 3-fold catenated MOFs (NU-1351 and NU-1352) with rare 3,6-connected cml-c3 nets. Lastly, the differences in the topology of NU-1350 and NU-1351/NU-1352 could be attributed to the slight distortions of the shorter linker in the former from the ideal trigonal prism geometry to an octahedral geometry when coordinated to the trigonal planar uranyl nodes.
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