Active template synthesis

IF 40.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Chemical Society Reviews Pub Date : 2024-09-05 DOI:10.1039/D4CS00430B
Romain Jamagne, Martin J. Power, Zhi-Hui Zhang, Germán Zango, Benjamin Gibber and David A. Leigh
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Abstract

The active template synthesis of mechanically interlocked molecular architectures exploits the dual ability of various structural elements (metals or, in the case of metal-free active template synthesis, particular arrangements of functional groups) to serve as both a template for the organisation of building blocks and as a catalyst to facilitate the formation of covalent bonds between them. This enables the entwined or threaded intermediate structure to be covalently captured under kinetic control. Unlike classical passive template synthesis, the intercomponent interactions transiently used to promote the assembly typically do not ‘live on’ in the interlocked product, meaning that active template synthesis can be traceless and used for constructing mechanically interlocked molecules that do not feature strong binding interactions between the components. Since its introduction in 2006, active template synthesis has been used to prepare a variety of rotaxanes, catenanes and knots. Amongst the metal–ion-mediated versions of the strategy, the copper(I)-catalysed alkyne–azide cycloaddition (CuAAC) remains the most extensively used transformation, although a broad range of other catalytic reactions and transition metals also provide effective manifolds. In metal-free active template synthesis, the recent discovery of the acceleration of the reaction of primary amines with electrophiles through the cavity of crown ethers has proved effective for forming an array of rotaxanes without recognition elements, including compact rotaxane superbases, dissipatively assembled rotaxanes and molecular pumps. This Review details the active template concept, outlines its advantages and limitations for the synthesis of interlocked molecules, and charts the diverse set of reactions that have been used with this strategy to date. The application of active template synthesis in various domains is discussed, including molecular machinery, mechanical chirality, catalysis, molecular recognition and various aspects of materials science.

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主动模板合成。
机械联锁分子结构的活性模板合成利用了各种结构元素(金属或在无金属活性模板合成的情况下,特定的官能团排列)的双重能力,既可作为组织构件的模板,又可作为促进构件之间形成共价键的催化剂。这样,缠绕或螺纹状的中间结构就能在动力学控制下被共价俘获。与传统的被动模板合成不同,用于促进组装的瞬时组分间相互作用通常不会 "存留 "在互锁产物中,这意味着主动模板合成可以是无迹可寻的,并可用于构建机械互锁分子,而这些分子的各组分之间并不具有很强的结合相互作用。自 2006 年问世以来,活性模板合成法已被用于制备各种轮烷、猫烷和结。在该策略的金属离子介导版本中,铜(I)催化的炔吖啶环加成(CuAAC)仍然是使用最广泛的转化方法,尽管其他多种催化反应和过渡金属也提供了有效的歧管。在无金属活性模板合成中,最近发现的通过冠醚空腔加速伯胺与亲电物反应的方法已被证明可有效形成一系列无识别元素的轮烷,包括紧凑型轮烷超级碱、耗散组装轮烷和分子泵。本综述详细介绍了活性模板的概念,概述了它在合成互锁分子方面的优势和局限性,并描绘了迄今为止使用这种策略进行的各种反应。文章讨论了活性模板合成在各个领域的应用,包括分子机械、机械手性、催化、分子识别和材料科学的各个方面。
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来源期刊
Chemical Society Reviews
Chemical Society Reviews 化学-化学综合
CiteScore
80.80
自引率
1.10%
发文量
345
审稿时长
6.0 months
期刊介绍: Chemical Society Reviews is published by: Royal Society of Chemistry. Focus: Review articles on topics of current interest in chemistry; Predecessors: Quarterly Reviews, Chemical Society (1947–1971); Current title: Since 1971; Impact factor: 60.615 (2021); Themed issues: Occasional themed issues on new and emerging areas of research in the chemical sciences
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