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自组装配位笼中结构和功能复杂性的增加。

Increasing structural and functional complexity in self-assembled coordination cages.

作者信息

Pullen Sonja, Tessarolo Jacopo, Clever Guido H

机构信息

Department of Chemistry and Chemical Biology, TU Dortmund University Otto-Hahn-Straße 6 44227 Dortmund Germany

Homogeneous, Supramolecular and Bio-Inspired Catalysis, Van't Hoff Institute for Molecular Sciences, University of Amsterdam Science Park 904 1098 XH Amsterdam The Netherlands

出版信息

Chem Sci. 2021 May 10;12(21):7269-7293. doi: 10.1039/d1sc01226f.

Abstract

Progress in metallo-supramolecular chemistry creates potential to synthesize functional nano systems and intelligent materials of increasing complexity. In the past four decades, metal-mediated self-assembly has produced a wide range of structural motifs such as helicates, grids, links, knots, spheres and cages, with particularly the latter ones catching growing attention, owing to their nano-scale cavities. Assemblies serving as hosts allow application as selective receptors, confined reaction environments and more. Recently, the field has made big steps forward by implementing dedicated functionality, catalytic centres or photoswitches to allow stimuli control. Besides incorporation in homoleptic systems, composed of one type of ligand, desire arose to include more than one function within the same assembly. Inspiration comes from natural enzymes that congregate, for example, a substrate recognition site, an allosteric regulator element and a reaction centre. Combining several functionalities without creating statistical mixtures, however, requires a toolbox of sophisticated assembly strategies. This review showcases the implementation of function into self-assembled cages and devises strategies to selectively form heteroleptic structures. We discuss first examples resulting from a combination of both principles, namely multicomponent multifunctional host-guest complexes, and their potential in application in areas such as sensing, catalysis, and photo-redox systems.

摘要

金属超分子化学的进展为合成功能日益复杂的纳米系统和智能材料创造了潜力。在过去的四十年里,金属介导的自组装产生了各种各样的结构基序,如螺旋体、网格、链、结、球体和笼状结构,尤其是后者因其纳米级的空腔而受到越来越多的关注。作为主体的组装体可作为选择性受体、受限反应环境等应用。最近,该领域通过引入专用功能、催化中心或光开关以实现刺激控制取得了重大进展。除了纳入由一种配体组成的同配体系外,人们还希望在同一组装体中包含多种功能。灵感来自天然酶,例如,天然酶聚集了一个底物识别位点、一个变构调节元件和一个反应中心。然而,要在不产生统计混合物的情况下组合多种功能,需要一套复杂的组装策略工具箱。本综述展示了功能在自组装笼状结构中的实现,并设计了选择性形成杂配结构的策略。我们讨论了结合这两种原理产生的首个实例,即多组分多功能主客体复合物,以及它们在传感、催化和光氧化还原系统等领域的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557b/8171321/4a98c8e6b85d/d1sc01226f-f1.jpg

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