Li Qiaowei, Zhang Wenyu, Miljanić Ognjen S, Sue Chi-Hau, Zhao Yan-Li, Liu Lihua, Knobler Carolyn B, Stoddart J Fraser, Yaghi Omar M
Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA.
Science. 2009 Aug 14;325(5942):855-9. doi: 10.1126/science.1175441.
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.
到目前为止,金属有机框架(MOFs)的应用在很大程度上依赖于与客体小分子的非特异性结合相互作用。我们使用了含有34元和36元大环聚醚的长有机支柱(约2纳米)作为识别模块,构建了几种晶体原始立方框架,这些框架以一种在被动、开放网状几何结构中未观察到的方式进行特异性结合。MOF-1001能够以立体电子控制的方式将百草枯二价阳离子(PQT2+)客体对接在大环内。这种特异性络合行为定量地产生了相应的MOF-1001准轮烷,这通过对MOF-1001、其准轮烷及其分子支柱前体进行的X射线衍射以及固态和溶液态核磁共振光谱研究得到证实。一项对照实验试图将PQT2+纳入不含聚醚支柱的框架(MOF-177)中,结果显示PQT2+的摄取量可忽略不计,这表明大环聚醚在PQT2+对接中的重要性。