Publication | Closed Access
Synthesis, Functionalization and Reductive Degradation of Multibrominated Disulfide-containing Hyperbranched Polymers
13
Citations
40
References
2011
Year
Macromolecular ChemistryEngineeringOrganic ChemistryChemistryPolymersChemical EngineeringMacromolecular EngineeringReductive DegradationAlkyl Bromide GroupsStar CopolymersPolymer ChemistryEthylene OxideSynthetic MacromoleculeBiopolymersPolymer ReactionBiomolecular EngineeringDepolymerizationPolymer SciencePolymerization KineticsFunctional MaterialsPolymer Synthesis
Reductively degradable hyperbranched polymethacrylates with multiple peripheral alkyl bromide groups were synthesized by the azobis(2-isobutyronitrile)-initiated copolymerization of diethylene glycol methyl ether methacrylate or oligo(ethylene oxide) methyl ether methacrylate with the disulfide-containing crosslinker bis(2-methacryloyloxyethyl)disulfide (2.5–10.0 mol-% relative to the monomer) in the presence of carbon tetrabromide (10–40-fold excess relative to the radical initiator) as efficient chain transfer agent. The alkyl bromide groups initiated the atom-transfer radical polymerization of methyl methacrylate, and star copolymers with hyperbranched disulfide-containing cores were formed. Both the macroinitiators and the star copolymers derived from them were degraded in reducing environment.
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