Chemistry

[ASAP] Linker-Flexibility-Induced Triangular Antiprism Nodes in a Three-Dimensional Covalent Organic Framework

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This study reports the synthesis of a three-dimensional covalent organic framework (COF) in which flexible linker molecules adopt conformations that generate triangular antiprism nodes, a geometry rarely observed in COF architectures. The linker flexibility plays a central role in directing the self-assembly toward this unusual nodal geometry, resulting in a well-defined 3D porous network. The work expands the known topological diversity of COFs by demonstrating that controlled conformational freedom in building blocks can be exploited as a design principle for accessing non-default net topologies.


Expanding the topological diversity of COFs is important because framework topology directly governs properties such as pore geometry, surface area, and guest uptake behavior, which are critical for applications in gas storage, separation, and heterogeneous catalysis. This finding provides a new design strategy for constructing complex 3D porous materials with tailored architectures.


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Journal of the American Chemical Society
DOI: 10.1021/jacs.6c06539

Source: [ASAP] Linker-Flexibility-Induced Triangular Antiprism Nodes in a Three-Dimensional Covalent Organic Framework