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通过不对称配体立体异构体的阴离子模板自组装形成的复杂低对称银胶囊。

Intricate Low-Symmetry Ag Capsules Formed by Anion-Templated Self-Assembly of the Stereoisomers of an Unsymmetric Ligand.

作者信息

Tashiro Shohei, Yamada Yoshihiko, Kringe Lea Antonia, Okajima Yoshiki, Shionoya Mitsuhiko

机构信息

Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.

出版信息

J Am Chem Soc. 2024 Dec 18;146(50):34501-34509. doi: 10.1021/jacs.4c11583. Epub 2024 Dec 1.

Abstract

Metal-organic cages and capsules exhibit space-specific functions based on their discrete hollow structures. To acquire enzyme-like asymmetric or intricate structures, they have been modified by desymmetrization with two or more different ligands. There is a need to establish new strategies that can desymmetrize structures in a simple way using only one type of ligand, which is different from the mixed-ligand approach. In this study, a strategy was developed to form interconvertible stereoisomers using the unsymmetric macrocyclic ligand benzimidazole[3]arene. Single-crystal X-ray diffraction analysis revealed that the isomers assembled with silver tetrafluoroborate afforded a conformationally heteroleptic Ag capsule with an intricate structure. The six Ag ions in the capsule were desymmetrized, resulting in significantly different coordination geometries. Remarkably, the capsule encapsulates a single tetrafluoroborate anion via multipoint C-H···F-B hydrogen bonds in both the solid and solution states, suggesting that anions of appropriate size and shape can act as a template for the capsule formation. These results demonstrate that the use of isomerizable and unsymmetric ligands is the effectiveness of constructing highly dissymmetric supramolecular structures from a single ligand.

摘要

金属有机笼和胶囊基于其离散的中空结构展现出空间特异性功能。为了获得类似酶的不对称或复杂结构,它们已通过用两种或更多种不同配体进行去对称化修饰。需要建立新的策略,该策略能够仅使用一种类型的配体以简单的方式使结构去对称化,这与混合配体方法不同。在本研究中,开发了一种使用不对称大环配体苯并咪唑[3]芳烃形成可相互转化的立体异构体的策略。单晶X射线衍射分析表明,与四氟硼酸银组装的异构体提供了一种具有复杂结构的构象杂配银胶囊。胶囊中的六个银离子被去对称化,导致配位几何结构显著不同。值得注意的是,该胶囊在固态和溶液状态下均通过多点C-H···F-B氢键包封单个四氟硼酸根阴离子,这表明尺寸和形状合适的阴离子可作为胶囊形成的模板。这些结果表明,使用可异构化的不对称配体对于从单一配体构建高度不对称的超分子结构是有效的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2965/11664504/84601fa1c6ed/ja4c11583_0001.jpg

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