5.2 Ionic polymerization: cationic and anionic mechanisms
2 min read•Last Updated on July 23, 2024
Ionic polymerization involves charged active centers, either positive (cationic) or negative (anionic). These mechanisms offer precise control over polymer properties but require specific monomers and careful reaction conditions.
Compared to free radical methods, ionic polymerization allows for better molecular weight control and complex architectures. However, it's more sensitive to impurities and has a narrower range of suitable monomers.
Ionic Polymerization Mechanisms
Cationic vs anionic polymerization mechanisms
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Top images from around the web for Cationic vs anionic polymerization mechanisms
Photocatalytic carbanion generation from C–H bonds – reductant free Barbier/Grignard-type ... View original
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Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening ... View original
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Frontiers | Molecular Orbital Insights of Transition Metal-Stabilized Carbocations View original
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Photocatalytic carbanion generation from C–H bonds – reductant free Barbier/Grignard-type ... View original
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Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening ... View original
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Cationic polymerization
Formation and propagation of positively charged active centers (carbocations) through addition of monomers
Initiated by strong acids (sulfuric acid, perchloric acid) or Lewis acids (aluminum chloride, boron trifluoride)
Termination occurs via chain transfer or combination with a counterion
Anionic polymerization
Formation and propagation of negatively charged active centers (carbanions) through addition of monomers
Initiated by strong bases (sodium hydroxide, potassium hydroxide) or electron transfer agents (sodium naphthalene)
Termination occurs via chain transfer or reaction with impurities (water, carbon dioxide)
Monomers for ionic polymerization
Monomers suitable for cationic polymerization
Contain electron-donating substituents that stabilize the carbocation (isobutylene, vinyl ethers, N-vinylcarbazole, styrene)
Monomers suitable for anionic polymerization
Contain electron-withdrawing substituents that stabilize the carbanion (styrene, butadiene, isoprene, methyl methacrylate, acrylonitrile)
Components of ionic polymerization
Initiators
Generate active centers (carbocations or carbanions) to start polymerization
Strong acids for cationic (hydrochloric acid, sulfuric acid), strong bases or electron transfer agents for anionic (n-butyllithium, sodium naphthalene)
Co-initiators
Assist in formation of active centers and control polymerization rate
Water, alcohols, ethers for cationic; alkali metal alkoxides for anionic
Solvents
Provide medium for polymerization reaction and influence stability of active centers and polymerization rate
Low polarity solvents for cationic (hexane, toluene), polar aprotic solvents for anionic (tetrahydrofuran, dioxane)
Ionic vs free radical polymerization
Advantages of ionic polymerization
Better control over molecular weight and molecular weight distribution
Ability to produce block copolymers and other complex architectures
Lower polymerization temperatures and faster reaction rates
Absence of chain transfer and termination by combination
Limitations of ionic polymerization
Sensitive to impurities (moisture, oxygen) and require stringent reaction conditions
Limited monomer scope compared to free radical polymerization
More expensive due to need for high-purity reagents and solvents
Difficulty controlling stereochemistry of resulting polymer