Self-assembled hexacationic cages enhance anion binding properties, indicating potential for anion capture.
Two types of supramolecular cages were synthesized in high yields via a self-assembled dynamic organic reaction: tricationic cages, PT3+/MT3+, and hexacationic cages, PH6+/MH6+. The formar imine cages are only stable in their in situ self-assembly solutions and showed limited anion recognition. In contrast, the latter hydrazone cages are kinetically inert and isolable as solid-state compounds via counterion exchange. The hexacationic cages exhibited significantly enhanced anion binding properties. For example, both PH6+ and MH6+ with chloride counterions can recognize Br-, NO3- and SO42- in aqueous media, where these anions are considered highly hydrated.
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Wu et al. (2025) studied this question.
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