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Responsive Anionophores with AND Logic Multi-Stimuli Activation
Manzoor Ahmad1, Toby G Johnson1, Martin Flerin1
1Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK.
Angewandte Chemie (International Ed. in English)
|March 22, 2024
Summary
Researchers developed novel stimuli-responsive ion transporters using dynamic hydrogen bonding. These advanced systems offer precise control over ion transport activation by light, redox, or enzymes for targeted applications.
Area of Science:
- Supramolecular Chemistry
- Chemical Biology
- Materials Science
Background:
- Artificial ion transport systems show promise for anticancer therapeutics and treating channelopathies.
- Stimuli-responsive systems with spatiotemporal control for targeted applications are scarce.
Purpose of the Study:
- To create a modular platform for stimuli-responsive ion transporters.
- To achieve precise OFF-ON activation of ion transport using various external stimuli.
Main Methods:
- Utilized dynamic hydrogen bonding interactions of a 4,6-dihydroxy-isophthalamide core.
- Alkylated hydroxyl groups with stimulus-responsive moieties to create 'caged' transporters.
- Employed orthogonal stimuli for multi-stimuli activation (AND logic).
Main Results:
- Developed ion transporters activated by light, redox, and enzymes with excellent OFF-ON profiles.
- Demonstrated that cleavage of stimulus-responsive cages reverses hydrogen bonding, forming an anion binding cavity.
- Achieved multi-stimuli activation requiring two orthogonal triggers for transport initiation.
Conclusions:
- The modular platform enables facile post-functionalization for targeted activation with multiple triggers.
- This strategy provides a versatile approach to designing sophisticated, stimuli-responsive ion transport systems.
- The developed transporters hold potential for advanced applications in chemotherapeutics and beyond.
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