阳离子聚合
金属有机骨架
化学
分子
有机分子
金属
纳米技术
分子识别
对接(动物)
组合化学
材料科学
有机化学
医学
吸附
护理部
作者
Qiaowei Li,Wenyu Zhang,Ognjen Š. Miljanić,Andrew C.‐H. Sue,Yanli Zhao,Lihua Liu,Carolyn B. Knobler,J. Fraser Stoddart,Omar M. Yaghi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2009-08-13
卷期号:325 (5942): 855-859
被引量:383
标识
DOI:10.1126/science.1175441
摘要
The use of metal-organic frameworks (MOFs) so far has largely relied on nonspecific binding interactions to host small molecular guests. We used long organic struts (approximately 2 nanometers) incorporating 34- and 36-membered macrocyclic polyethers as recognition modules in the construction of several crystalline primitive cubic frameworks that engage in specific binding in a way not observed in passive, open reticulated geometries. MOF-1001 is capable of docking paraquat dication (PQT2+) guests within the macrocycles in a stereoelectronically controlled fashion. This act of specific complexation yields quantitatively the corresponding MOF-1001 pseudorotaxanes, as confirmed by x-ray diffraction and by solid- and solution-state nuclear magnetic resonance spectroscopic studies performed on MOF-1001, its pseudorotaxanes, and their molecular strut precursors. A control experiment involving the attempted inclusion of PQT2+ inside a framework (MOF-177) devoid of polyether struts showed negligible uptake of PQT2+, indicating the importance of the macrocyclic polyether in PQT2+ docking.
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