多面体
化学
对称(几何)
各向同性
金属
纳米技术
分子对称性
化学物理
自组装
分子
结晶学
计算化学
有机化学
几何学
物理
材料科学
量子力学
数学
作者
Charlie T. McTernan,Jack A. Davies,Jonathan R. Nitschke
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2022-04-18
卷期号:122 (11): 10393-10437
被引量:176
标识
DOI:10.1021/acs.chemrev.1c00763
摘要
The field of metallosupramolecular chemistry has advanced rapidly in recent years. Much work in this area has focused on the formation of hollow self-assembled metal-organic architectures and exploration of the applications of their confined nanospaces. These discrete, soluble structures incorporate metal ions as 'glue' to link organic ligands together into polyhedra.Most of the architectures employed thus far have been highly symmetrical, as these have been the easiest to prepare. Such high-symmetry structures contain pseudospherical cavities, and so typically bind roughly spherical guests. Biomolecules and high-value synthetic compounds are rarely isotropic, highly-symmetrical species. To bind, sense, separate, and transform such substrates, new, lower-symmetry, metal-organic cages are needed. Herein we summarize recent approaches, which taken together form the first draft of a handbook for the design of higher-complexity, lower-symmetry, self-assembled metal-organic architectures.
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