Demonstrates effective control of self-assembly in metallosupramolecular structures, indicating high conversion efficiency and stability.
Coordination‐driven self‐assembly is a facile and powerful strategy for the construction of metallosupramolecular mechanically interlocked molecules (MIMs). However, the limited stability of most MIMs constitutes a challenge with respect to the evaluation of their practical applications. Herein, we demonstrate a rational strategy to control the self‐assembly outcome for selected metallosupramolecular structures. The reaction of a biphenyl‐bridged bisimidazole ligand with dinuclear building blocks of varying lengths leads, depending on the size of the dinuclear building block, to a simple [1+1] metallacycle, a twisted [2+2] three‐dimensional trapezoidal structure, or an intricate [3+3] metallosupramolecular trefoil knot. The trefoil knot exhibits exceptional structural stability, resisting decomposition upon dilution in polar solvent. Its knotted topology enforces strong intramolecular π⋅⋅⋅π stacking interactions, which red‐shift the absorption band into the near‐infrared (NIR) region. Benefiting from its stability and NIR absorption, the trefoil knot displays a high photothermal conversion efficiency ( η = 73.5%) and a potent photoacoustic (PA) effect in water, even at low concentrations.
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Lu et al. (2025) studied this question.
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