Self-Assembly of Organic Cages into 1D and 2D Hierarchical Superstructures Driven by Halogen-Bonding Interactions

被引:2
|
作者
Wang, Yixin [1 ]
Mu, Gui-Fang [1 ]
Sun, Kuang-Shi [2 ]
Yang, Nan [1 ]
Yan, Qiang [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
来源
ACS MATERIALS LETTERS | 2024年 / 6卷 / 08期
基金
中国国家自然科学基金;
关键词
NANOPARTICLES;
D O I
10.1021/acsmaterialslett.4c00928
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
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 (Ph3P=O)-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 P=O<middle dot><middle dot><middle dot>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.
引用
收藏
页码:3667 / 3674
页数:8
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