Paper
Thiol-yne ‘click’/coupling chemistry and recent applications in polymer and materials synthesis and modification
Published Oct 23, 2014 · A. Lowe
Polymer
Q1 SJR score
245
Citations
2
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Highly CitedStudy Snapshot
The thiol-yne reaction has recently been applied in polymer synthesis and modification, as well as small molecule (bio)organic chemistry, gaining interest in various research areas.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
ROMP (co)polymers with pendent alkyne side groups: post-polymerization modification employing thiol–yne and CuAAC coupling chemistries
ROMP copolymers with pendent alkyne functional groups can be modified using thiol-yne and CuAAC coupling chemistries for various applications.
2014·13citations·J. A. V. Hensbergen et al.·Polymer Chemistry
Polymer Chemistry
Thiol–ene “click” reactions and recent applications in polymer and materials synthesis: a first update
Thiol-ene "click" chemistry has been successfully applied in polymer and materials synthesis and modification, advancing advanced macromolecular engineering and materials chemistry.
2014·511citations·A. Lowe·Polymer Chemistry
Polymer Chemistry
Metal‐Catalyzed and Metal‐Free Alkyne Hydrothiolation: Synthetic Aspects and Application Trends
Alkyne hydrothiolation is a valuable tool for preparing sulfur-containing compounds like vinyl thioethers with high efficiency and selectivity, and the photoinduced free-radical approach is a complementary tool for complex biomolecular systems.
2014·81citations·A. Dondoni et al.·European Journal of Organic Chemistry
European Journal of Organic Chemistry
Directing cell migration using micropatterned and dynamically adhesive polymer brushes.
This study developed a novel technique to create dynamically adhesive micropatterned substrates, allowing precise control of cell adhesion and migration over space and time.
2014·44citations·Patricia Costa et al.·Acta biomaterialia
Acta biomaterialia
High refractive index polyvinylsulfide materials prepared by selective radical mono-addition thiol–yne chemistry
Selective radical mono-addition thiol-yne chemistry produces high-refractive index polyvinyl sulfide materials with high optical transparency and low dispersions, making them ideal for light reflection and chromatic dispersion applications.
2014·51citations·R. Pötzsch et al.·Polymer Chemistry
Polymer Chemistry
Citations
Development of a thiol-maleimide crosslinked carboxymethyl guar gum hydrogel for sustained drug delivery
CMG-based hydrogels show promising potential for sustained and controlled delivery of gastrointestinal drugs, with pH-dependent swelling and excellent biocompatibility.
2025·0citations·R. Alnoman et al.·Journal of Drug Delivery Science and Technology
Journal of Drug Delivery Science and Technology
Micellar “Click” Nanoreactors: Spiking Pluronic-Based Micelles with Polymeric Ligands
Spiking pluronic-based micelles with polymeric ligands significantly increases CuAAC reaction rates, providing valuable insights into designing efficient catalytic nanoreactors.
2024·0citations·Krishna Vippala et al.·Macromolecules
Macromolecules
Expanding (Bio)Conjugation Strategies: Metal-Free Thiol-Yne Photo-Click Reaction for Immobilization onto PLLA Surfaces
The thiol-yne click reaction effectively immobilizes biomolecules onto PLLA surfaces, enhancing bioconjugation strategies and advancing biomedical technologies.
2024·0citations·Julia Sánchez-Bodón et al.·Coatings
Coatings
Preparation and study of novel UV‐curable alkyd‐siloxane coating materials
UV-curable alkyd-siloxane coatings, based on alkyd oligomers and oligoorganosilsesquioxanes, can be cured in 5 minutes, increasing hydrophobicity and thermal stability, while 30 times faster than classical alkyd curing methods
2024·1citation·Artem A. Golubev et al.·Journal of Applied Polymer Science
Journal of Applied Polymer Science
Sulfobetaine Zwitterions with Embedded Fluorocarbons: Synthesis and Interfacial Properties.
Fluorinated sulfobetaine (FSB) zwitterionic polymers with embedded fluorocarbons show increased hydrophobicity, reduced oil-water interfacial tension, and stability in aqueous environments.
2024·2citations·Carla G Steppan et al.·ACS macro letters
ACS macro letters