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基于功能大环和分子笼的阴离子识别导向超分子催化

Anion Recognition-Directed Supramolecular Catalysis with Functional Macrocycles and Molecular Cages.

作者信息

Wang Qi-Qiang

机构信息

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Acc Chem Res. 2024 Nov 5;57(21):3227-3240. doi: 10.1021/acs.accounts.4c00583. Epub 2024 Oct 25.

Abstract

ConspectusThe development of supramolecular chemistry has provided a variety of host molecules and noncovalent tools for boosting catalytic processes, stimulating the emergence and advance of supramolecular catalysis, among which macrocyclic and cage-like compounds have attracted great attention due to their possession of an enzyme-mimetic cavity and recognition ability. While the privileged scaffolds such as crown ethers, cyclodextrins, cucurbiturils, calixarenes, and metal-coordinated cages have been widely used, their skeletons usually do not contain a directional binding site; binding and activation mainly rely on cation-associated interactions or hydrophobic effects. In this context, the recent advance of anion supramolecular chemistry has drawn our attention to developing an anion recognition-directed approach by using tailor-made functionalized macrocycles and cages. Anions are important widely existing species in both biological and chemical systems and play an important role in regulating the structure and function of enzymes. We envisioned that by taking advantage of anions, including their rich variety, diverse geometry, and multiple interaction sites, the sophisticated cooperation of multiple noncovalent interactions can be manipulated in a confined cavity for directing efficient and selective catalysis.Following this concept, we initiated our study by introducing typical thiourea H-bonding groups to design and synthesize a series of bis-thiourea macrocycles, especially chiral macrocycles, by incorporating chiral linkers. Taking advantage of the obtained strong, cooperative anion binding, a macrocycle-enabled counteranion trapping strategy was developed, which afforded greatly enhanced catalytic efficiency and excellent stereocontrol in acid-catalyzing reactions. Furthermore, inspired by sulfate-induced macrocyclic dimerization assembly, we built a substrate-induced assembly system, enabling an induced-fit cooperative activation network for efficient and enantioselective catalysis. In addition, anion recognition-driven chirality gearing with a more sophisticated trithiourea cage was revealed, which could provide a basis for implementing anion-triggered allosteric catalysis within the induced helical space. Not limited to hydrogen bonding, the emerging anion-π interactions were largely exploited. A series of triazine-based prism cages containing three V-shaped electron-deficient π-cavities were constructed, and their anion-π binding properties were studied. Based on this system, cooperative anion-π activation was established for driving highly efficient and selective catalysis, which paved a way to push anion-π interactions toward more practical and useful catalyst design.These results demonstrated that the anion-recognition direction can serve as a powerful, versatile approach for boosting highly efficient and selective supramolecular catalysis. It is feasible not only for employing exogenous anions (e.g., counteranion) as a handle but also for recognition and regulation of anionic active intermediates/transition states, from use in conventional H-bonding to emerging anion-π recognition.

摘要

综述

超分子化学的发展为促进催化过程提供了多种主体分子和非共价工具,推动了超分子催化的出现和发展。其中,大环化合物和笼状化合物因其具有类似酶的空腔和识别能力而备受关注。虽然冠醚、环糊精、葫芦脲、杯芳烃和金属配位笼等优势骨架已被广泛应用,但其骨架通常不包含定向结合位点;结合和活化主要依赖于阳离子相关相互作用或疏水效应。在此背景下,阴离子超分子化学的最新进展使我们关注通过使用定制的功能化大环和笼来开发一种阴离子识别导向方法。阴离子是生物和化学系统中广泛存在的重要物种,在调节酶的结构和功能方面发挥着重要作用。我们设想,通过利用阴离子,包括其丰富的种类、多样的几何形状和多个相互作用位点,可以在受限的空腔中操纵多种非共价相互作用的复杂协同作用,以实现高效和选择性催化。

遵循这一概念,我们通过引入典型的硫脲氢键基团开始研究,通过引入手性连接基设计并合成了一系列双硫脲大环,特别是手性大环。利用所获得的强协同阴离子结合作用,开发了一种大环介导的抗衡阴离子捕获策略,该策略在酸催化反应中提供了大大提高的催化效率和优异的立体控制。此外受硫酸根诱导的大环二聚体组装的启发,我们构建了一个底物诱导组装系统,实现了一个诱导契合的协同活化网络,用于高效和对映选择性催化。此外,还揭示了与更复杂的三硫脲笼的阴离子识别驱动的手性齿轮作用,这可为在诱导的螺旋空间内实现阴离子触发的变构催化提供基础。不限于氢键作用,新兴的阴离子-π相互作用也得到了大量利用。构建了一系列含有三个V形缺电子π-空腔的基于三嗪的棱柱笼,并研究了它们的阴离子-π结合性质。基于该系统,建立了协同阴离子-π活化作用以驱动高效和选择性催化,这为将阴离子-π相互作用推向更实际和有用的催化剂设计铺平了道路。

这些结果表明,阴离子识别导向可作为一种强大、通用的方法来促进高效和选择性超分子催化。它不仅可行,可将外源阴离子(如抗衡阴离子)用作手段,还可用于识别和调控阴离子活性中间体/过渡态,从传统的氢键作用到新兴的阴离子-π识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2e/11669085/6814bbc4e235/ar4c00583_0001.jpg

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