Institute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.
Chem Soc Rev. 2014 Aug 21;43(16):5700-34. doi: 10.1039/c4cs00106k.
The assembly of metal ions with organic ligands through the formation of coordination bonds gives crystalline framework materials, known as metal-organic frameworks (MOFs), which recently emerged as a new class of porous materials. Besides the structural designability of MOFs at the molecular length scale, the researchers in this field very recently made important advances in creating more complex architectures at the mesoscopic/macroscopic scale, in which MOF nanocrystals are used as building units to construct higher-order superstructures. The structuring of MOFs in such a hierarchical order certainly opens a new opportunity to improve the material performance via design of the physical form rather than altering the chemical component. This review highlights these superstructures and their applications by categorizing them into four dimensionalities, zero-dimensional (0D), one-dimensional (1D), two-dimensional (2D), and three-dimensional (3D) superstructures. Because the key issue for structuring of MOFs is to spatially control the nucleation process in desired locations, this review conceptually categorizes the available synthetic methodologies from the viewpoint of the reaction system.
通过形成配位键将金属离子与有机配体组装在一起,得到了结晶骨架材料,即金属-有机骨架(MOFs),它最近成为一类新的多孔材料。除了 MOFs 在分子长度尺度上的结构可设计性之外,该领域的研究人员最近在介观/宏观尺度上创造更复杂结构方面取得了重要进展,其中将 MOF 纳米晶体用作构建单元来构建更高阶的超结构。MOFs 按这种层次结构进行结构化,无疑为通过设计物理形式而不是改变化学组成来改善材料性能开辟了新的机会。通过将它们分为零维 (0D)、一维 (1D)、二维 (2D) 和三维 (3D) 超结构,这篇综述强调了这些超结构及其应用。由于 MOFs 结构化的关键问题是在所需位置空间控制成核过程,因此,从反应体系的角度来看,本综述从概念上对现有的合成方法进行了分类。