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.
    SYSNO ASEP0508824
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevSolvent-control over monomer distribution in the copolymerization of 2-oxazolines and the effect of a gradient structure on self-assembly
    Tvůrce(i) Bera, D. (BE)
    Sedlacek, O. (BE)
    Jäger, Eliezer (UMCH-V) ORCID, RID
    Pavlova, Ewa (UMCH-V) RID
    Vergaelen, M. (BE)
    Hoogenboom, R. (BE)
    Zdroj.dok.Polymer Chemistry . - : Royal Society of Chemistry - ISSN 1759-9954
    Roč. 10, č. 37 (2019), s. 5116-5123
    Poč.str.8 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovagradient copolymers ; poly(2-oxazoline)s ; solvent-controlled monomer distribution
    Vědní obor RIVCD - Makromolekulární chemie
    Obor OECDPolymer science
    CEPGA17-09998S GA ČR - Grantová agentura ČR
    TN01000008 GA TA ČR - Technologická agentura ČR
    Způsob publikováníOmezený přístup
    Institucionální podporaUMCH-V - RVO:61389013
    UT WOS000487564000008
    EID SCOPUS85072656412
    DOI10.1039/C9PY00927B
    Anotacene-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.
    PracovištěÚstav makromolekulární chemie
    KontaktEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Rok sběru2020
    Elektronická adresahttps://pubs.rsc.org/en/content/articlelanding/2019/PY/C9PY00927B#!divAbstract
Počet záznamů: 1  

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