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Published on: June 8, 2016
Controlled Formation of Star Polymer Nanoparticles via Visible Light Photopolymerization
Thomas G McKenzie1, Edgar H H Wong1, Qiang Fu1
1Polymer Science Group, Department of Chemical and Biomolecular Engineering, The University of Melbourne, Parkville 3010, Melbourne, Australia.
A new visible light polymerization method synthesizes star polymers using trithiocarbonates. This technique efficiently creates complex polymer architectures like core cross-linked star and miktoarm stars with high precision.
Area of Science:
- Polymer Chemistry
- Materials Science
- Organic Synthesis
Background:
- Visible light mediated photopolymerization offers precise control over polymer synthesis.
- Trithiocarbonates are established reversible-deactivation radical polymerization (RCRP) agents.
- Developing efficient one-pot methods for complex polymer architectures is a key challenge.
Purpose of the Study:
- To synthesize well-defined core cross-linked star (CCS) polymer nanoparticles using a novel visible light photopolymerization technique.
- To investigate the formation of (pseudo)miktoarm stars via an "in-out" approach.
- To demonstrate the high efficiency and control offered by trithiocarbonate-mediated photopolymerization.
Main Methods:
- Utilizing visible light to mediate radical polymerization controlled solely by trithiocarbonates.
- Employing a one-pot synthesis strategy for creating star polymer structures.
- Investigating the reinitiation capability of photoactive trithiocarbonate moieties within the star core.
Main Results:
- Successful synthesis of core cross-linked star (CCS) polymer nanoparticles with high end-group fidelity.
- Achieved high monomer conversion and yield in a one-pot procedure.
- Demonstrated efficient "in-out" synthesis of (pseudo)miktoarm stars with 95% initiation efficiency.
Conclusions:
- Visible light mediated photopolymerization with trithiocarbonates provides a powerful and efficient route to complex polymer architectures.
- The method allows for precise control over polymer structure and high initiation efficiency.
- This technique opens new avenues for the "in-out" synthesis of advanced polymer nanostructures.
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