Yan Yun, Huang Jianbin, Tang Ben Zhong
Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory for Structural Chemistry of Unstable and Stable Species, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
Chem Commun (Camb). 2016 Oct 14;52(80):11870-84. doi: 10.1039/c6cc03620a. Epub 2016 Aug 5.
Supramolecular self-assembly into various nano- or microscopic structures based on non-covalent interactions between molecules has been recognized as a very efficient approach that leads to functional materials. Since most non-covalent interactions are relatively weak and form and break without significant activation barriers, the thermodynamic equilibrium of many supramolecular systems can be easily influenced by processing pathways that allow the system to stay in a kinetically trapped state. Thus far, kinetic traps have been found to be very important in producing more elaborate structural and functional diversity of self-assembled systems. In this review, we try to summarize the approaches that can produce kinetically trapped self-assemblies based on examples made by us. We focus on the following subjects: (1) supramolecular pathway dependent self-assembly, including kinetically trapped self-assemblies facilitated by host-guest chemistry, coordination chemistry, and electrostatic interactions; (2) physical processing pathway dependent self-assembly, including solvent quality controlled self-assembly, evaporation induced self-assembly and crystallization induced self-assembly.
基于分子间非共价相互作用的超分子自组装形成各种纳米或微观结构,已被认为是一种非常有效的制备功能材料的方法。由于大多数非共价相互作用相对较弱,其形成和断裂无需显著的活化能垒,许多超分子体系的热力学平衡很容易受到加工途径的影响,这些途径可使体系处于动力学捕获状态。到目前为止,人们发现动力学捕获在产生更精细的自组装体系结构和功能多样性方面非常重要。在这篇综述中,我们试图根据我们所举的例子总结能够产生动力学捕获自组装体的方法。我们关注以下主题:(1)依赖超分子途径的自组装,包括由主客体化学、配位化学和静电相互作用促进的动力学捕获自组装;(2)依赖物理加工途径的自组装,包括溶剂质量控制的自组装、蒸发诱导自组装和结晶诱导自组装。