Key Lab of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084, People's Republic of China.
Acc Chem Res. 2012 Apr 17;45(4):608-18. doi: 10.1021/ar200226d. Epub 2012 Jan 13.
The process of self-assembly spontaneously creates well-defined structures from various chemical building blocks. Self-assembly can include different levels of complexity: it can be as simple as the dimerization of two small building blocks driven by hydrogen bonding or as complicated as a cell membrane, a remarkable supramolecular architecture created by a bilayer of phospholipids embedded with functional proteins. The study of self-assembly in simple systems provides a fundamental understanding of the driving forces and cooperativity behind these processes. Once the rules are understood, these guidelines can facilitate the research of highly complex self-assembly processes. Among the various components for self-assembly, an amphiphilic molecule, which contains both hydrophilic and hydrophobic parts, forms one of the most powerful building blocks. When amphiphiles are dispersed in water, the hydrophilic component of the amphiphile preferentially interacts with the aqueous phase while the hydrophobic portion tends to reside in the air or in the nonpolar solvent. Therefore, the amphiphiles aggregate to form different molecular assemblies based on the repelling and coordinating forces between the hydrophilic and hydrophobic parts of the component molecules and the surrounding medium. In contrast to conventional amphiphiles, supra-amphiphiles are constructed on the basis of noncovalent interactions or dynamic covalent bonds. In supra-amphiphiles, the functional groups can be attached to the amphiphiles by noncovalent synthesis, greatly speeding their construction. The building blocks for supra-amphiphiles can be either small organic molecules or polymers. Advances in the development of supra-amphiphiles will not only enrich the family of conventional amphiphiles that are based on covalent bonds but will also provide a new kind of building block for the preparation of complex self-assemblies. When polymers are used to construct supra-amphiphiles, the resulting molecules are known as superamphiphiles. This Account will focus on the use of amphiphiles and supra-amphiphiles for self-assembly at different levels of complexity. We introduce strategies for the fabrication of robust assemblies through self-assembly of amphiphiles. We describe the supramolecular approach for the molecular design of amphiphiles through the enhancement of intermolecular interaction among the amphiphiles. In addition, we describe polymerization under mild conditions to stabilize the assemblies formed by self-assembly of amphiphiles. Finally, we highlight self-assembly methods driven by noncovalent interactions or dynamic covalent bonds for the fabrication of supra-amphiphiles with various topologies. Further self-assembly of supra-amphiphiles provides new building blocks for complex structures, and the dynamic nature of the supra-amphiphiles endows the assemblies with stimuli-responsive functions.
自组装过程可以从各种化学构建块自发地创建具有明确定义的结构。自组装可以包括不同程度的复杂性:它可以像两个小构建块通过氢键驱动的二聚化一样简单,也可以像细胞膜一样复杂,细胞膜是由嵌入功能性蛋白质的双层磷脂组成的卓越的超分子结构。对简单体系中自组装的研究为这些过程背后的驱动力和协同作用提供了基本的理解。一旦理解了规则,这些指导原则就可以促进对高度复杂的自组装过程的研究。在各种自组装成分中,两亲分子包含亲水和疏水部分,是最强大的构建块之一。当两亲分子分散在水中时,两亲分子的亲水部分优先与水相相互作用,而疏水部分则倾向于位于空气或非极性溶剂中。因此,两亲分子根据组成分子的亲水和疏水部分与周围介质之间的排斥和协调力聚集形成不同的分子组装体。与传统的两亲分子相比,超两亲分子是基于非共价相互作用或动态共价键构建的。在超两亲分子中,功能基团可以通过非共价合成连接到两亲分子上,从而大大加快其构建速度。超两亲分子的构建块可以是小分子有机分子或聚合物。超两亲分子的发展不仅丰富了基于共价键的传统两亲分子家族,而且为复杂自组装的制备提供了一种新的构建块。当聚合物用于构建超两亲分子时,所得分子称为超两亲分子。本专题将重点介绍在不同复杂程度下使用两亲分子和超两亲分子进行自组装的情况。我们介绍了通过自组装两亲分子制造坚固组装体的策略。我们描述了通过增强两亲分子之间的分子间相互作用进行两亲分子的分子设计的超分子方法。此外,我们描述了在温和条件下进行聚合以稳定由两亲分子自组装形成的组装体的方法。最后,我们强调了通过非共价相互作用或动态共价键驱动的自组装方法来制造具有各种拓扑结构的超两亲分子。超两亲分子的进一步自组装为复杂结构提供了新的构建块,并且超两亲分子的动态特性赋予了组装体对刺激的响应功能。