Self-Assembly of Organic Cages into 1D and 2D Hierarchical Superstructures Driven by Halogen-Bonding Interactions
卤素
材料科学
卤键
纳米技术
自组装
结晶学
化学物理
化学
有机化学
烷基
作者
Yixin Wang,Gui‐Fang Mu,Kuangshi Sun,Nan Yang,Qiang Yan
出处
期刊:ACS materials letters [American Chemical Society] 日期:2024-07-15卷期号:: 3667-3674被引量:2
标识
DOI:10.1021/acsmaterialslett.4c00928
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···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.