Abstract

Water-soluble cationic macromonomers of (dimethylamino)ethyl methacrylate (DMAEMA) with terminal diallylmethylammonium or allylmethylphenylammonium group were synthesized by nitrogen anion (nitroanion) initiated living anionic polymerization of DMAEMA and subsequent quaternization. The initiators, lithium diallyamide and lithium allylphenylamide, were prepared by the reaction of corresponding N-substituted allylamine with butyllithium. The substituents on the nitroanion had a significant effect on the initiation efficiency. The initiator efficiencies of lithium allylamide, diallylamide, and allylphenylamide increased by the order 0 < 25% < 79% at −78 °C. The low initiator efficiency of lithium diallylamide was due to the reaction of the nitroanion with carbonyl groups in the monomer and polymer and could not be improved by optimizing polymerization conditions. A capping method using dimethylacrylamide (DMA) or tert-butyl methacrylate (tBMA) was then developed to modify the lithium diallylamide and thereby...

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.