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基于大环的固态超分子聚合物。

Macrocycle-Based Solid-State Supramolecular Polymers.

机构信息

State Key Laboratory of Chemical Engineering, Stoddart Institute of Molecular Science, Department of Chemistry, Zhejiang University, Hangzhou 310027, China.

ZJU-Hangzhou Global Scientific and Technological Innovation Center, Hangzhou 311215, China.

出版信息

Acc Chem Res. 2022 Apr 5;55(7):1025-1034. doi: 10.1021/acs.accounts.2c00011. Epub 2022 Mar 24.

Abstract

Supramolecular polymers, generated by connecting monomers through noncovalent interactions, have received considerable attention over the past years, as they provide versatile platforms for developing diverse aesthetically pleasing polymeric structures with promising applications in a variety of fields, such as medicine, catalysis, and sensing. In the development of supramolecular polymers, macrocyclic hosts play a very important role. Benefiting from their abundant host-guest chemistry and self-assembly characteristics, macrocycles themselves or their host-guest complexes can self-assemble to form well-ordered supramolecular polymeric architectures including pseudopolyrotaxanes and polyrotaxanes. The integration of these topological structures into supramolecular polymeric materials also imbues them with some unforeseen functions. Current interest in macrocycle-based supramolecular polymers is mostly focused on the development of supramolecular soft materials in solution or gel-state, in which the dynamic nature of noncovalent interactions endows supramolecular polymers with a wealth of "smart" properties, such as multiresponsiveness and self-repair capabilities. While preparation of macrocycle-derived supramolecular polymers in the solid state is a relatively challenging but intriguing prospect, they are an important part of the field of supramolecular polymers. On one hand, the construction of macrocycle-based solid-state supramolecular polymers enables us to obtain new materials with novel properties and functions such as mechano-responsiveness. On the other hand, the molecular structures and arrangements in these materials are well-identified by X-ray crystallography techniques, offering a direct visual representation of the supramolecular polymerization process. The analysis of the role of noncovalent interactions in these architectures allows us to design more sophisticated and elegant supramolecular polymers in a highly rationalized and controllable manner. This Account serves to summarize the research progress on macrocycle-based solid-state supramolecular polymers (MSSPs), including the contributions toward this field made by our group. For constructing MSSPs, the key point is to control noncovalent interactions. Thus, in this Account, we primarily classify these MSSPs by different noncovalent interactions involved to connect the monomers, including metal-ligand interactions, host-guest interactions, π···π stacking, and halogen bonding. These noncovalent interactions are highly associated with the structures and functions of the resultant MSSPs. For instance, using metal-ligand interactions as driving forces, metal clusters can be introduced in MSSPs which afford systems with solid-state luminescence or proton conduction properties; supramolecular polymerization using macrocycle-based host-guest interactions can modulate the molecular arrangement of some specific molecules in the solid state, which further influences their solid-state properties; π···π stacking interactions and halogen bonding give chemists more choice to design MSSPs with various elements. The role of macrocyclic hosts in MSSPs is also revealed in these descriptions. Finally, the remaining challenges are identified for further development of future prospects. We hope that this Account can inspire new discoveries in the realm of supramolecular functional systems and offer new opportunities for the construction of supramolecular architectures and solid-state materials.

摘要

超分子聚合物通过非共价相互作用连接单体而产生,近年来受到了相当大的关注,因为它们为开发具有多种美感的聚合结构提供了多功能平台,这些聚合结构在医学、催化和传感等多个领域具有广阔的应用前景。在超分子聚合物的发展中,大环主体起着非常重要的作用。大环主体由于其丰富的主客体化学和自组装特性,自身或其主客体配合物可以自组装形成有序的超分子聚合结构,包括拟聚轮烷和聚轮烷。将这些拓扑结构集成到超分子聚合物材料中,也赋予了它们一些意想不到的功能。目前,基于大环的超分子聚合物的研究主要集中在开发溶液或凝胶态中的超分子软材料上,其中非共价相互作用的动态性质赋予超分子聚合物丰富的“智能”特性,如多重响应性和自修复能力。虽然大环衍生的超分子聚合物在固态中的制备是一个相对具有挑战性但又很有趣的前景,但它们是超分子聚合物领域的一个重要组成部分。一方面,构建基于大环的固态超分子聚合物使我们能够获得具有新颖性能和功能的新材料,例如机械响应性。另一方面,这些材料中的分子结构和排列可以通过 X 射线晶体学技术来识别,为超分子聚合过程提供了直接的可视化表示。分析非共价相互作用在这些结构中的作用,可以使我们以高度合理化和可控的方式设计更复杂和优雅的超分子聚合物。本综述旨在总结基于大环的固态超分子聚合物(MSSP)的研究进展,包括我们小组对此领域的贡献。为了构建 MSSP,控制非共价相互作用是关键。因此,在本综述中,我们主要根据连接单体的不同非共价相互作用对这些 MSSP 进行分类,包括金属-配体相互作用、主体-客体相互作用、π···π 堆积和卤键。这些非共价相互作用与所得 MSSP 的结构和功能密切相关。例如,利用金属-配体相互作用作为驱动力,可以将金属簇引入 MSSP 中,从而赋予系统固态发光或质子传导性能;利用大环主体-客体相互作用进行超分子聚合,可以调节某些特定分子在固态中的分子排列,从而进一步影响它们的固态性能;π···π 堆积相互作用和卤键为化学家提供了更多选择,可用于设计具有各种元素的 MSSP。大环主体在 MSSP 中的作用也在这些描述中得到了揭示。最后,确定了进一步发展未来前景的剩余挑战。我们希望本综述能够激发在超分子功能系统领域的新发现,并为构建超分子架构和固态材料提供新的机会。

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