Macromonomers, telechelics and more complex architectures of PMA by a combination of biphasic SET-LRP and biphasic esterification. Issue 14 (2nd March 2018)

• Record Type: Journal Article
• Authors: Moreno, Adrian; Jezorek, Ryan L.; Liu, Tong; Galià, Marina; Lligadas, Gerard; Percec, Virgil
• Is Part Of: Polymer chemistry. Volume 9:Issue 14(2018)
• Page Start: 1885
• Page End: 1899
• Publication Date: 2018-03-02
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c8py00150b
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : Macromonomers and telechelics of PMA via biphasic SET-LRP and biphasic esterification with potassium acrylate. Abstract : The high bromine chain end functionality of polyacrylates synthesized by single electron transfer living radical polymerization (SET-LRP) mediated by TREN in a biphasic acetone–water mixture containing Cu(ii )Br2 can be exploited to introduce specific functional groups to the chain-ends of these polymers. Here, the α-bromoester end groups of poly(methyl acrylate) (PMA ) synthesized in this biphasic SET-LRP system using non-activated Cu(0) wire as catalyst were reacted also under heterogeneous biphasic conditions with potassium acrylate to yieldPMA macromonomers and telechelics with α- and α, ω-acrylate chain ends. The reagents used in both steps are air insensitive and inexpensive. 500 MHz 1 H NMR, GPC and MALDI-TOF analyses in combination with the thio-bromo "click" reaction were used to confirm the high efficiency of this two-step protocol. The reactive nature of these macromonomers by the preparation of aPMA- g -PMA more complex architecture was also demonstrated.