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Synthesis of new amphiphilic cationic block copolymers and study of their behaviour in aqueous medium as regards hydrophobic microdomain formation

Identifieur interne : 001B24 ( Main/Exploration ); précédent : 001B23; suivant : 001B25

Synthesis of new amphiphilic cationic block copolymers and study of their behaviour in aqueous medium as regards hydrophobic microdomain formation

Auteurs : A. Fischer [France] ; A. Brembilla [France] ; P. Lochon [France]

Source :

RBID : ISTEX:509C67308D5C2D3B3F134B93C3BC00B673A83169

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English descriptors

Abstract

Abstract: Block copolymers of N-hexadecyl-4-vinylpyridinium bromide (4VPC16Br) and N,N-dimethylacrylamide (DMAA) were synthesised by nitroxide-mediated radical polymerisation using 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) as a control agent. The behaviour of such block copolymers in aqueous medium was then investigated in relation to the respective size of both the amphiphilic and the hydrophobic block. Viscosimetry, surface tension measurements, and fluorescence spectroscopy revealed that intramolecular hydrophobic microdomains were spontaneously formed by the pendent long alkyl chains. The properties of the corresponding microdomains were determined in terms of polarity and local cohesion, and were revealed to depend on the relative length of the blocks in the copolymer.

Url:
DOI: 10.1016/S0032-3861(00)00493-6


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Le document en format XML

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<div type="abstract" xml:lang="en">Abstract: Block copolymers of N-hexadecyl-4-vinylpyridinium bromide (4VPC16Br) and N,N-dimethylacrylamide (DMAA) were synthesised by nitroxide-mediated radical polymerisation using 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) as a control agent. The behaviour of such block copolymers in aqueous medium was then investigated in relation to the respective size of both the amphiphilic and the hydrophobic block. Viscosimetry, surface tension measurements, and fluorescence spectroscopy revealed that intramolecular hydrophobic microdomains were spontaneously formed by the pendent long alkyl chains. The properties of the corresponding microdomains were determined in terms of polarity and local cohesion, and were revealed to depend on the relative length of the blocks in the copolymer.</div>
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