Počet záznamů: 1  

Solvent-control over monomer distribution in the copolymerization of 2-oxazolines and the effect of a gradient structure on self-assembly

  1. 1.
    0508824 - ÚMCH 2020 RIV GB eng J - Článek v odborném periodiku
    Bera, D. - Sedlacek, O. - Jäger, Eliezer - Pavlova, Ewa - Vergaelen, M. - Hoogenboom, R.
    Solvent-control over monomer distribution in the copolymerization of 2-oxazolines and the effect of a gradient structure on self-assembly.
    Polymer Chemistry. Roč. 10, č. 37 (2019), s. 5116-5123. ISSN 1759-9954. E-ISSN 1759-9962
    Grant CEP: GA ČR(CZ) GA17-09998S; GA TA ČR(CZ) TN01000008
    Institucionální podpora: RVO:61389013
    Klíčová slova: gradient copolymers * poly(2-oxazoline)s * solvent-controlled monomer distribution
    Obor OECD: Polymer science
    Impakt faktor: 5.342, rok: 2019
    Způsob publikování: Omezený přístup
    https://pubs.rsc.org/en/content/articlelanding/2019/PY/C9PY00927B#!divAbstract

    ne-pot synthesis of gradient copolymers by statistical copolymerization represents an elegant route to amphiphilic copolymers as a basis for micellar systems. Herein, we propose a robust strategy to control the monomer distribution along the gradient copolymer chain by appropriate selection of the polymerization solvent. The gradient formation was investigated for copolymerizations of the hydrophilic 2-methyl-2-oxazoline (MeOx) and the hydrophobic 2-phenyl-2-oxazoline (PhOx) using sulfolane and acetonitrile as the polymerization solvents revealing a striking difference. In sulfolane, a quasi-block (CP2) like character was observed, whereas acetonitrile led to a more gradient-like (CP3) copolymer. The monomer distribution was found to have an impact on the micellization behavior of both amphiphilic copolymers, which was also compared with the analogous block copolymer (CP1). CP1 led to the formation of the smallest micelles, followed by a somewhat larger structure formed by CP2, while CP3 self-assembles into significantly larger nanoparticles. These findings open up a route to new amphiphilic copolymer systems with precisely fine-tuned architecture.
    Trvalý link: http://hdl.handle.net/11104/0300011

     
     
Počet záznamů: 1  

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