Articles producció científica> Química Analítica i Química Orgànica

Macromonomers, telechelics and more complex architectures of PMA by a combination of biphasic SET-LRP and biphasic esterification

  • Dades identificatives

    Identificador: imarina:5132120
    Autors:
    Moreno, AdrianJezorek, Ryan L.Liu, TongGalia, MarinaLligadas, GerardPercec, Virgil
    Resum:
    © 2018 The Royal Society of Chemistry. 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 yield PMA macromonomers and telechelics with α- and α,ω-acrylate chain ends. The reagents used in both steps are air insensitive and inexpensive. 500 MHz 1H 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 a PMA-g-PMA more complex architecture was also demonstrated.
  • Altres:

    Autor segons l'article: Moreno, Adrian; Jezorek, Ryan L.; Liu, Tong; Galia, Marina; Lligadas, Gerard; Percec, Virgil
    Departament: Química Analítica i Química Orgànica
    Autor/s de la URV: Galià Clua, Marina Teresa / Lligadas Puig, Gerard
    Paraules clau: Hashtag Etiqueta «#» @uroweb @residentesaeu @infoAeu
    Resum: © 2018 The Royal Society of Chemistry. 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 yield PMA macromonomers and telechelics with α- and α,ω-acrylate chain ends. The reagents used in both steps are air insensitive and inexpensive. 500 MHz 1H 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 a PMA-g-PMA more complex architecture was also demonstrated.
    Àrees temàtiques: Química Polymers and plastics Polymer science Organic chemistry Engenharias ii Biomedical engineering Bioengineering Biochemistry
    ISSN: 17599954
    Adreça de correu electrònic de l'autor: marina.galia@urv.cat gerard.lligadas@urv.cat
    Identificador de l'autor: 0000-0002-4359-4510 0000-0002-8519-1840
    Pàgina final: 1899
    Data d'alta del registre: 2024-09-07
    Volum de revista: 9
    Versió de l'article dipositat: info:eu-repo/semantics/submittedVersion
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Polymer Chemistry. 9 (14): 1885-1899
    Referència de l'ítem segons les normes APA: Moreno, Adrian; Jezorek, Ryan L.; Liu, Tong; Galia, Marina; Lligadas, Gerard; Percec, Virgil (2018). Macromonomers, telechelics and more complex architectures of PMA by a combination of biphasic SET-LRP and biphasic esterification. Polymer Chemistry, 9(14), 1885-1899. DOI: 10.1039/c8py00150b
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2018
    Pàgina inicial: 1885
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Biochemistry,Bioengineering,Biomedical Engineering,Organic Chemistry,Polymer Science,Polymers and Plastics
    Química
    Polymers and plastics
    Polymer science
    Organic chemistry
    Engenharias ii
    Biomedical engineering
    Bioengineering
    Biochemistry
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