Self-Assembly of Organic Cages into 1D and 2D Hierarchical Superstructures Driven by Halogen-Bonding Interactions
Great efforts have been devoted to designing organic molecular cages with a 3D topology and shape persistence. Yet, how to harness these cages as atomically precise, nanosized building blocks to construct hierarchical superstructures remains underexplored. Here we report a strategy that exploits fun...
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Veröffentlicht in: | ACS materials letters 2024-08, Vol.6 (8), p.3667-3674 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Great efforts have been devoted to designing organic molecular cages with a 3D topology and shape persistence. Yet, how to harness these cages as atomically precise, nanosized building blocks to construct hierarchical superstructures remains underexplored. Here we report a strategy that exploits functionalized organic cages as premade nanobuilding units and connects them into self-assemblies with structural hierarchy and tunable dimensionality. Using a triphenylphosphine oxide (Ph3PO)-paneled trigonal prism as vertex-decorated cage to connect with iodobenzene-capped bridging ligands (Ar–I), they can constitute infinite cage-based superstructures through weak PO···I–Ar halogen-bonding interactions. Regulating the ligand configuration and valence can dictate the connecting direction to form 1D cage-to-chain (nanofilament) and 2D cage-to-framework (nanosheet) architectures and further hierarchically assemble into microwire and microplate materials. The cage-connecting assemblies possess larger void volume and dual porosity compared to their parent cage itself, which can be applied in selective encapsulation and bisubstrate cascade catalysis. |
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ISSN: | 2639-4979 2639-4979 |
DOI: | 10.1021/acsmaterialslett.4c00928 |