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柱状大环主体 柱状芳烃:超分子化学的新主角。

Pillar-Shaped Macrocyclic Hosts Pillar[n]arenes: New Key Players for Supramolecular Chemistry.

机构信息

Graduate School of Natural Science and Technology, Kanazawa University , Kakuma-machi, Kanazawa 920-1192, Japan.

Japan Science and Technology Agency, PRESTO , 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

出版信息

Chem Rev. 2016 Jul 27;116(14):7937-8002. doi: 10.1021/acs.chemrev.5b00765. Epub 2016 Jun 23.


DOI:10.1021/acs.chemrev.5b00765
PMID:27337002
Abstract

In 2008, we reported a new class of pillar-shaped macrocyclic hosts, known as "pillar[n]arenes". Today, pillar[n]arenes are recognized as key players in supramolecular chemistry because of their facile synthesis, unique pillar shape, versatile functionality, interesting host-guest properties, and original supramolecular assembly characteristics, which have resulted in numerous electrochemical and biomedical material applications. In this Review, we have provided historical background to macrocyclic chemistry, followed by a detailed discussion of the fundamental properties of pillar[n]arenes, including their synthesis, structure, and host-guest properties. Furthermore, we have discussed the applications of pillar[n]arenes to materials science, as well as their applications in supramolecular chemistry, in terms of their fundamental properties. Finally, we have described the future perspectives of pillar[n]arene chemistry. We hope that this Review will provide a useful reference for researchers working in the field and inspire discoveries concerning pillar[n]arene chemistry.

摘要

2008 年,我们报道了一类新型的柱状大环主体,称为“柱[n]芳烃”。如今,由于其易于合成、独特的柱状形状、多功能性、有趣的主客体性质以及原始的超分子组装特性,柱[n]芳烃已成为超分子化学的关键参与者,这导致了许多电化学和生物医学材料的应用。在这篇综述中,我们提供了大环化学的历史背景,然后详细讨论了柱[n]芳烃的基本性质,包括它们的合成、结构和主客体性质。此外,我们还讨论了柱[n]芳烃在材料科学中的应用,以及它们在超分子化学中的应用,从它们的基本性质方面进行了讨论。最后,我们描述了柱[n]芳烃化学的未来展望。我们希望这篇综述能为该领域的研究人员提供有用的参考,并激发对柱[n]芳烃化学的发现。

相似文献

[1]
Pillar-Shaped Macrocyclic Hosts Pillar[n]arenes: New Key Players for Supramolecular Chemistry.

Chem Rev. 2016-6-23

[2]
Stimuli-Responsive Supramolecular Assemblies Constructed from Pillar[ n]arenes.

Acc Chem Res. 2018-7-17

[3]
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[4]
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[5]
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Acc Chem Res. 2022-11-1

[6]
Recent advances in pillar[n]arenes: synthesis and applications based on host-guest interactions.

Chem Commun (Camb). 2016-7-19

[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Decoding the Interplay of Hydrogen Bonding, Dispersion, and Steric Interactions in Conformational Isomerism Among Functionalized Pillar[n]arenes.

J Phys Chem C Nanomater Interfaces. 2025-1-30

[2]
Hydrogen-bonded supramolecular polymer networks for effective removal of perchlorate in water via clustered hydrogen-bonding.

Nat Commun. 2025-7-14

[3]
Dimerization of pillar[5]arene: length-adaptive encapsulation of long-chain guests.

Chem Sci. 2025-7-3

[4]
Crown ether-cycloparaphenylene hybrid multimacrocycles: insights into supramolecular gas sensing and biological potential.

Chem Sci. 2025-6-18

[5]
Stable cationic nanobelts synthesized by chemical oxidation of methylene-bridged [6]cycloparaphenylene.

Chem Sci. 2025-4-23

[6]
Pillar[5]arene-based supramolecular assemblies application in artificial light-harvesting systems.

RSC Adv. 2025-4-10

[7]
Acyclic cucurbit[]uril bearing alkyl sulfate ionic groups.

Beilstein J Org Chem. 2025-4-3

[8]
High-affinity 1 : 2 recognition based on naphthyl-azocalix[4]arene and its application as a cleavable noncovalent connector in constructing responsive supramolecular polymeric materials.

Chem Sci. 2025-3-19

[9]
Enantioselective construction of inherently chiral pillar[5]arenes via palladium-catalysed Suzuki-Miyaura cross-coupling.

Nat Commun. 2025-3-10

[10]
Metallacycle-cored luminescent ionic liquid crystals with trigonal symmetry.

Chem Sci. 2025-2-17

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