Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1.
Chem Soc Rev. 2013 Feb 7;42(3):871-90. doi: 10.1039/c2cs35337g.
The study of traditional organic cavitands has been central in the development of supramolecular chemistry. As the field of supramolecular chemistry matures, a new class of cavitand, the metallocavitand, is quietly emerging. No central theme currently exists to unify these relatable supramolecules due to the structural diversity of metallocavitands. To provide a concrete foundation for future metallocavitand research, we define metallocavitands here as multimetallic complexes where metal coordination is necessary for cavity formation. This tutorial review highlights synthetic routes based on self-assembly and macrocycle-templating strategies to isolate bowl-shaped metallocavitands, and highlights interesting supramolecular phenomena observed with metallocavitands such as dimerization, host-guest encapsulation, catalysis, unique regioselective reactivity, and enantioselective guest recognition.
对传统有机主体化合物的研究一直是超分子化学发展的核心。随着超分子化学领域的成熟,一类新的主体化合物——金属主体化合物正在悄然出现。由于金属主体化合物的结构多样性,目前还没有一个中心主题将这些相关的超分子统一起来。为了为未来的金属主体化合物研究提供坚实的基础,我们在这里将金属主体化合物定义为多金属配合物,其中金属配位对于腔的形成是必要的。本综述重点介绍了基于自组装和大环模板策略的合成途径,以分离碗状金属主体化合物,并强调了观察到的有趣的超分子现象,如二聚化、主客体包封、催化、独特的区域选择性反应性和对映选择性客体识别。