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分子内阳离子-π相互作用构建碗状发光分子容器。

Intramolecular Cation-π Interactions Organize Bowl-Shaped, Luminescent Molecular Containers.

作者信息

He Jia, Bai Minggui, Xiao Xuedong, Qiu Shuai, Chen Wenzhuo, Li Jiaqi, Yu Yang, Tian Wei

机构信息

Shaanxi Key Laboratory of Macromolecular Science and Technology, Xi'an Key Laboratory of Hybrid Luminescent Materials and Photonic Device, MOE Key Laboratory of Material Physics and Chemistry under Extraordinary Conditions, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University., Xi'an, 710072, Shaanxi, P. R. China.

Center for Supramolecular Chemistry & Catalysis and Department of Chemistry, College of Science, Shanghai University, 99 Shang-Da Road, Shanghai, 200444, China.

出版信息

Angew Chem Int Ed Engl. 2024 May 13;63(20):e202402697. doi: 10.1002/anie.202402697. Epub 2024 Mar 15.

Abstract

Molecules with nonplanar architectures are highly desirable due to their unique topological structures and functions. We report here the synthesis of two molecular containers (1 ⋅ 3Br and 1 ⋅ 3Cl), which utilize intramolecular cation-π interactions to enforce macrocylic arrangements and exhibit high binding affinity and luminescent properties. Remarkably, the geometry of the cation-π interaction can be flexibly tailored to achieve a precise ring arrangement, irrespective of the angle of the noncovalent bonds. Additionally, the C-H⋅⋅⋅Br hydrogen bonds within the container are also conducive to stabilizing the bowl-shaped conformation. These bowl-shaped conformations were confirmed both in solution through NMR spectroscopy and in the solid state by X-ray studies. 1 ⋅ 3Br shows high binding affinity and selectivity: F>Cl, through C-H⋅⋅⋅X (X=F, Cl) hydrogen bonds. Additionally, these containers exhibited blue fluorescence in solution and yellow room-temperature phosphorescence (RTP) in the solid state. Our findings illustrate the utility of cation-π interactions in designing functional molecules.

摘要

具有非平面结构的分子因其独特的拓扑结构和功能而备受青睐。我们在此报告了两种分子容器(1·3Br和1·3Cl)的合成,它们利用分子内阳离子-π相互作用来强制形成大环排列,并表现出高结合亲和力和发光特性。值得注意的是,阳离子-π相互作用的几何形状可以灵活调整,以实现精确的环排列,而与非共价键的角度无关。此外,容器内的C-H···Br氢键也有助于稳定碗状构象。这些碗状构象通过核磁共振光谱在溶液中以及通过X射线研究在固态中得到了证实。1·3Br通过C-H···X(X = F,Cl)氢键显示出高结合亲和力和选择性:F>Cl。此外,这些容器在溶液中表现出蓝色荧光,在固态中表现出黄色室温磷光(RTP)。我们的研究结果说明了阳离子-π相互作用在设计功能分子中的实用性。

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