Solvent-Triggered Fast and Visible Switching between Cage- and Channel-Type Hydrogen-Bonded Organic Frameworks

The inherent weak bonding nature of hydrogen-bonded organic frameworks (HOFs) performs like a double-edged sword in that it endows HOFs with superiority in processability and dynamicity but deactivates its on-demand controllability in the crystalline phase. Herein, based on the synergy of dynamic H-bonding interactions and the tailored low solubility in common organic solvents, reversible and fast topological transitions between cage- and channel-type HOFs were achieved upon immersing in the solution state. The aggregation-induced-emission character of the tecton facilitates the visualization of the elusive initial transition process with high sensitivity. In addition, the visible transition from cage- and channel-type HOFs to thermally stable crystalline phases is also achieved under thermal induction.