Poly(N-isopropyl acrylamide)-block-poly(n-butyl acrylate) thermoresponsive amphiphilic copolymers: Synthesis, characterization and self-assembly behavior in aqueous solutions

被引:29
|
作者
Skvarla, Juraj [1 ]
Zednik, Jiri [1 ]
Slouf, Miroslav [2 ]
Pispas, Stergios [3 ]
Stepanek, Miroslav [1 ]
机构
[1] Charles Univ Prague, Fac Sci, Dept Phys & Macromol Chem, Prague 12840 2, Czech Republic
[2] Acad Sci Czech Republic, Inst Macromol Chem, CR-16206 Prague 6, Czech Republic
[3] Natl Hellen Res Fdn, Inst Theoret & Phys Chem, GR-11635 Athens, Greece
关键词
Thermoresponsive block copolymers; Poly(N-isopropyl acrylamide); Light scattering; Association; POLY N-ISOPROPYLACRYLAMIDE; PHASE-TRANSITION; DIBLOCK COPOLYMERS; LIGHT-SCATTERING; WATER; MACROMOLECULES; AGGREGATION; MICELLES; CHAINS; PNIPAM;
D O I
10.1016/j.eurpolymj.2014.10.002
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report on the synthesis of poly(N-isopropyl acrylamide)-block-poly(n-butyl acrylate) (PNIPAm-b-PnBA) amphiphilic block copolymers and their temperature-responsive self-assembly behavior in aqueous solution. Well-defined PNIPAm-b-PnBA copolymers have been synthesized by a two-step RAFT polymerization scheme. The self-assembly behavior was studied by means of static and dynamic light scattering, H-1 NMR and fluorescence spectroscopy and transmission electron microscopy. The results show that already below the lower critical solution temperature (LCST) of PNIPAm, association of the PNIPAm blocks with hydrophobic dodecyl end groups of the charge transfer agent leads to the formation of loose aggregates of PNIPAm-b-PnBA micelles, the size and density of which increase with the increasing length of the PNIPAm block: The collapse of the PNIPAm blocks above the LCST leads to the decrease of the aggregates' size and the increase of their density, but the collapsed PNIPAm chains do not allow for interpenetration of the micellar shells and no further aggregation occurs. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:124 / 132
页数:9
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