Shape memory behavior of biocompatible polyurethane stereoelastomers synthesized via thiol-yne Michael addition

Keyphrases

• Alkenes 100%
• Stereochemistry 100%
• Urethane 100%
• Polyurethane 100%
• Biocompatibility 100%
• Degradation Properties 100%
• Michael Addition 100%
• Shape Memory Effect 100%
• Thiol-yne 100%
• Hydrogen Bonds (H-bonds) 50%
• Mechanical Properties 50%
• Glass Transition Temperature 50%
• Tensile Strength 50%
• Degradable 50%
• Nucleophilic 50%
• Bulk Properties 50%
• Implantable Devices 50%
• Drug Delivery 50%
• Dithiols 50%
• Organic Solvents 50%
• In Vitro Degradation 50%
• Organic Bases 50%
• Nucleophilic Addition 50%
• Device Fabrication 50%
• Drug-device 50%
• Polymer Backbone 50%
• Targeted Degradation 50%
• α,β-unsaturated Carbonyl Compounds 50%
• Soft Tissue Engineering 50%
• Shape Memory Elastomers 50%
• Solvent Polarity 50%

Material Science

• Polyurethane 100%
• Shape Memory 100%
• Ultimate Tensile Strength 33%
• Hydrogen Bonding 33%
• Glass Transition Temperature 33%
• Polymerization 33%
• Medical Implant 33%
• Elastomer 33%
• Device Fabrication 33%
• Nucleophilic Addition 33%