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Updated: Apr 25, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Monotelechelic poly(p-phenylenevinylene)s by ring opening metathesis polymerisation.
Benjamin J Lidster1, Jonathan M Behrendt, Michael L Turner
1Organic Materials Innovation Centre, School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK. Michael.Turner@Manchester.ac.uk.
High molecular weight poly(p-phenylenevinylene)s (PPVs) with reactive end groups were synthesized. These functionalized PPVs serve as effective macroinitiators for atom transfer radical polymerization of methyl methacrylate.
Area of Science:
- Polymer Chemistry
- Materials Science
Background:
- Poly(p-phenylenevinylene)s (PPVs) are conjugated polymers with unique optoelectronic properties.
- Controlled synthesis of PPVs with specific end-group functionality is crucial for advanced applications.
Purpose of the Study:
- To synthesize poly(p-phenylenevinylene)s (PPVs) with single reactive end groups.
- To evaluate the effectiveness of these functionalized PPVs as macroinitiators in controlled polymerization techniques.
Main Methods:
- Synthesis of PPVs with high molecular weights and narrow polydispersities.
- Functionalization of PPV chain ends with α-bromoester groups.
- Utilizing the functionalized PPVs in atom transfer radical polymerization (ATRP).
Main Results:
- Successfully prepared PPVs with controlled molecular weights and narrow polydispersities.
- Achieved excellent end-group functionality (f).
- Demonstrated that α-bromoester functionalized PPVs are effective macroinitiators for ATRP of methyl methacrylate (MMA).
Conclusions:
- Single reactive end-group functionalized PPVs can be synthesized with high precision.
- These PPVs are versatile macroinitiators for controlled polymer synthesis, enabling the creation of block copolymers and other complex architectures.
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