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Related Concept Videos

Ziegler–Natta Chain-Growth Polymerization: Overview01:17

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Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
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Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
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Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
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Related Experiment Video

Updated: Nov 20, 2025

Synthesis of Soft Polysiloxane-urea Elastomers for Intraocular Lens Application
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Azido-Functionalized Polyurethane Designed for Making Tunable Elastomers by Click Chemistry.

Xiaochu Ding1, Jin Gao2, Abhinav P Acharya3

  • 1Nancy E. and Peter C. Meining School of Biomedical Engineering, Cornell University, 277 Kimball Hall, Hollister Drive 134, Ithaca, New York 14853, United States.

ACS Biomaterials Science & Engineering
|January 19, 2021
PubMed
Summary
This summary is machine-generated.

Researchers developed a novel azido-functionalized polyurethane prepolymer for creating stable, tunable elastomers via click chemistry. This biomaterial offers excellent mechanical properties and biocompatibility for biomedical device applications.

Keywords:
azido functionalityclick chemistryelastomerspolyurethanescaffolds

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Area of Science:

  • Biomaterials Science
  • Polymer Chemistry
  • Biomedical Engineering

Background:

  • Polyurethanes are widely used biomaterials in biomedical engineering.
  • Current methods for polyurethane modification can involve toxic reagents or postmodification steps.

Purpose of the Study:

  • To develop a novel azido-functionalized polyurethane prepolymer.
  • To create stable porous elastomers using click chemistry, avoiding toxic polyisocyanates.
  • To investigate the tunable mechanical properties and biocompatibility of the resulting elastomers.

Main Methods:

  • Synthesis of an azido-functionalized polyurethane prepolymer.
  • Cross-linking via click chemistry using the prepolymer to form porous and compact elastomers.
  • Mechanical property testing (Young's modulus, strain at break, cyclic deformation).
  • Assessment of material stability in basic solution and in vivo biocompatibility via subcutaneous implantation in mice.

Main Results:

  • The prepolymer readily formed stable porous elastomers through click chemistry.
  • Mechanical properties, including Young's modulus (0.52–2.02 MPa for porous, up to 28.8 MPa for compact), were tunable.
  • Elastomers exhibited high strain at break (150%) and excellent fatigue resistance (1000 cycles).
  • The material demonstrated stability in basic solution and good in vivo biocompatibility with minimal inflammatory response.

Conclusions:

  • A novel, easily synthesized azido-functionalized polyurethane prepolymer enables the creation of tunable, high-performance elastomers.
  • The click chemistry approach avoids toxic reagents and allows for property modulation.
  • The material's mechanical properties, stability, and biocompatibility suggest its potential for biomedical device components.