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      Intramolecular Cation‐π Interactions Organize Bowl‐Shaped, Luminescent Molecular Containers

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          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.

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          Anion Recognition and Sensing: The State of the Art and Future Perspectives

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            Accurately extracting the signature of intermolecular interactions present in the NCI plot of the reduced density gradient versus electron density.

            An electron density (ED)-based methodology is developed for the automatic identification of intermolecular interactions using pro-molecular density. The expression of the ED gradient in terms of atomic components furnishes the basis for the Independent Gradient Model (IGM). This model leads to a density reference for non interacting atoms/fragments where the atomic densities are added whilst their interaction turns off. Founded on this ED reference function that features an exponential decay also in interference regions, IGM model provides a way to identify and quantify the net ED gradient attenuation due to interactions. Using an intra/inter uncoupling scheme, a descriptor (δg(inter)) is then derived that uniquely defines intermolecular interaction regions. An attractive feature of the IGM methodology is to provide a workflow that automatically generates data composed solely of intermolecular interactions for drawing the corresponding 3D isosurface representations.
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              Building on architectural principles for three-dimensional metallosupramolecular construction.

              Over the last two decades the field of metallosupramolecular self-assembly has emerged as a promising research area for the development of intricate, three-dimensional structures of increasing complexity and functionality. The advent of this area of research has strongly benefited from design principles that considered the ligand geometry and metal coordination geometry, thus opening up routes towards rationally designed classical (Archimedean or Platonic) architectures. In this tutorial review, we will focus on more recent developments in the design and synthesis of three-dimensional suprastructures which have non-classical architectures (non-Archimedean/Platonic solids) and we will explicitly address the secondary effects responsible for their formation. Three classes of metallosupramolecular assemblies will be discussed: architectures formed through the combination of a single ligand and metal, heteroleptic structures and heterometallic structures. It is hoped that our exposition may suggest how different principles employed in these three classes of structures might be combined to create even greater complexity and potential for function.
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                Author and article information

                Contributors
                Journal
                Angewandte Chemie International Edition
                Angew Chem Int Ed
                Wiley
                1433-7851
                1521-3773
                May 13 2024
                March 15 2024
                May 13 2024
                : 63
                : 20
                Affiliations
                [1 ] 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
                [2 ] Center for Supramolecular Chemistry & Catalysis and Department of Chemistry, College of Science Shanghai University 99 Shang-Da Road Shanghai 200444 China
                Article
                10.1002/anie.202402697
                aa589f56-a754-448c-bdfb-816f1f7f5fc3
                © 2024

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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