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Allosteric effects are common in biology, but have not been fully explored in the control of supramolecular polymerization. Herein, ditopic UPy derivatives with acyclic crown ether-like spacers were designed and… Click to show full abstract
Allosteric effects are common in biology, but have not been fully explored in the control of supramolecular polymerization. Herein, ditopic UPy derivatives with acyclic crown ether-like spacers were designed and synthesized, which can undergo supramolecular polymerization through quadruple hydrogen bonding. Upon the addition of K+, drastic molecular conformational change to the U-shape is induced by metal-coordination, reconfiguring remote UPy sites towards the formation of discrete cyclic dimers. Interestingly, the supramolecular polymerization can be restored by simply removing K+ by water-extraction.
Journal Title: Chemical communications
Year Published: 2020
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