共 50 条
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
相关论文
共 50 条