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Self-Assembly of Asymmetric Poly(ethylene oxide)-block-Poly (n-butyl acrylate) Diblock Copolymers in Aqueous Media to Unexpected Morphologies
被引:51
|作者:
Petrov, Petar D.
[1
,2
]
Drechsler, Markus
[2
]
Mueller, Axel H. E.
[2
]
机构:
[1] Bulgarian Acad Sci, Inst Polymer, BU-1113 Sofia, Bulgaria
[2] Univ Bayreuth, Makromol Chem & Bayreuther Zentrum Kolloide & Gre, D-95440 Bayreuth, Germany
来源:
关键词:
AMPHIPHILIC BLOCK-COPOLYMERS;
TRANSFER RADICAL POLYMERIZATION;
MULTIPLE MORPHOLOGIES;
VESICLES;
MICELLIZATION;
MICELLES;
WATER;
D O I:
10.1021/jp809598v
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
We report on the aggregation behavior of asymmetric amphiphilic poly(ethylene oxide)-block-poly(n-butyl acrylate) (PEO-PnBA) diblock copolymers into vesicles and micelles in aqueous media. These copolymers are composed of a hydrophilic PEO block of a constant chain length of 113 monomer units and longer soft hydrophobic PnBA blocks of 163 and 243 units, respectively. This study presents the first insight into the solution properties of such copolymers examined by dynamic light scattering (DLS), cryogenic and conventional transmission electron microscopy (cryo-TEM, TEM), field-flow fractionation (FFF), and turbidity measurements. Whereas the block copolymer with the shorter PnBA block forms crew-cut micelles, for the polymer with the longer hydrophobic block, the morphology of the aggregates strongly depends on concentration. Besides crew-cut micelles, we observed very peculiar vesicular structures, in particular entrapped, multilamellar, and multicompartment vesicles. Although PnBA has a low glass transition temperature, the aggregates formed in water are kinetically frozen.
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页码:4218 / 4225
页数:8
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