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Updated: May 5, 2026

Chemoselective Modification of Viral Surfaces via Bioorthogonal Click Chemistry
Published on: August 19, 2012
Host-Guest Stimuli-Responsive Click Chemistry.
Arturo Blanco-Gómez1, Mauro Díaz-Abellás1, Iván Montes de Oca1
1CICA - Centro Interdisciplinar de Química e Bioloxía and Departamento de Química, Facultade de Ciencias, Universidade da Coruña, A Coruña, 15071, A Coruña, Spain.
Stimuli-responsive click chemistry utilizes host-guest interactions for reversible molecular ligation. This approach offers controlled binding and unbinding, advancing functional chemical synthesis.
Area of Science:
- Supramolecular Chemistry
- Organic Synthesis
Background:
- Traditional click chemistry offers irreversible molecular ligation but lacks reversibility.
- Limitations include side products, slow kinetics, and sensitivity to reaction conditions.
- Non-covalent click chemistry, using host-guest systems, provides a more efficient and controllable alternative.
Purpose of the Study:
- To review the implementation of molecular switches in non-covalent click chemistry.
- To introduce the concept of stimuli-responsive click chemistry.
- To highlight the potential for human-controlled molecular conjugation.
Main Methods:
- Discussion of host-guest self-assembled systems.
- Integration of molecular switches for external control.
- Analysis of thermodynamically regulated processes and extrinsic control mechanisms.
Main Results:
- Stimuli-responsive click chemistry enables reversible control over molecular binding states.
- Host-guest complexes facilitate stable yet labile non-covalent ligation.
- Demonstration of externally controlled molecular conjugation through selected examples.
Conclusions:
- Stimuli-responsive click chemistry mimics natural systems for controlled molecular assembly.
- This approach advances function-oriented chemical synthesis.
- Offers a powerful platform for developing human-controlled molecular conjugation strategies.
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