Abstract

Intramolecular chain transfer to polymer and subsequent propagation of tertiary radicals cause extensive branching in radical polymerization of acrylic monomers. Studies in the literature have shown that under controlled radical polymerization conditions the extent of branching is significantly reduced. There are two competing theories to explain this effect. In one, the cause of reduced branching is attributed to a reduction in the number of backbiting events, and in the other that has been specifically applied to atom-transfer radical polymerization (ATRP), the cause is due to trapping of the tertiary radical by a fast deactivation step. In this article we show that trapping of the tertiary radical is not the cause for the reduction in branching fraction. This is shown by the absence of the corresponding patched midchain bromide structure as revealed by quantitative 13C NMR and by the ability to chain extend from a poly(butyl acrylate-co-butyl 2-bromoacrylate) copolymer by ATRP. These results are comple...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.