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Well-defined poly(oxazoline)-b-poly(acrylate) amphiphilic copolymers: From synthesis by polymer-polymer coupling to self-organization in water
被引:24
|作者:
Guillerm, Brieuc
[1
]
Monge, Sophie
[1
]
Lapinte, Vincent
[1
]
Robin, Jean-Jacques
[1
]
机构:
[1] Univ Montpellier II Cc1702, Inst Charles Gerhardt Montpellier, CNRS, UMR5253,UM2,ENSCM,UM1,Equipe Ingn & Architectures, F-34095 Montpellier 5, France
关键词:
atom transfer radical polymerization;
polyoxazolines;
ring-opening polymerization;
self-assembly;
synthesis;
RING-OPENING POLYMERIZATION;
DIBLOCK COPOLYMERS;
BLOCK-COPOLYMERS;
POLY(2-OXAZOLINE)S;
BIODISTRIBUTION;
NANOPARTICLES;
CHEMISTRY;
MICELLES;
CLICKING;
ROUTE;
D O I:
10.1002/pola.26474
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
In this contribution, we report on the self-assembly in water of original amphiphilic poly(2-methyl-2-oxazoline)-b-poly(tert-butyl acrylate) copolymers, synthesized by copper-catalyzed azidealkyne cycloaddition (CuAAC) reaction. For such purpose, (poly(2-methyl-2-oxazoline)) and (poly(tert-butyl acrylate)) are first prepared by cationic ring-opening polymerization and atom transfer radical polymerization, respectively. Well-defined polymeric building blocks, omega-N3-P(t-BA) and a-alkyne-P(MOx), bearing reactive chain end groups, are accurately characterized by matrix-assisted laser desorption ionization time-of-flight spectroscopy. Then, P(MOx)n-b-P(t-BA)m are achieved by polymerpolymer coupling and are fully characterized by diffusion-ordered NMR spectroscopy and size exclusion chromatography, demonstrating the obtaining of pure amphiphilic copolymers. Consequently, the latter lead to the formation in water of well-defined monodisperse spherical micelles (RH = 4060 nm), which are studied by fluorescence spectroscopy, static light scattering, atomic force microscope, and transmission electronic microscopy. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013
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页码:1118 / 1128
页数:11
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