Heterotactic poly(N-isopropylacrylamide) prepared via radical polymerization in the presence of fluorinated alcohols

Radical polymerization of N-isopropylacrylamide in toluene at −40°C in the presence of fourfold amounts of fluorinated alcohols was investigated. The 13C NMR analysis of the obtained polymers suggested that the addition of fluorinated alcohols induced heterotactic specificity in radical polymerizati...

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Veröffentlicht in:Polymer (Guilford) 2007-08, Vol.48 (17), p.4921-4925
Hauptverfasser: Hirano, Tomohiro, Kamikubo, Takahiro, Okumura, Yuya, Sato, Tsuneyuki
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container_end_page 4925
container_issue 17
container_start_page 4921
container_title Polymer (Guilford)
container_volume 48
creator Hirano, Tomohiro
Kamikubo, Takahiro
Okumura, Yuya
Sato, Tsuneyuki
description Radical polymerization of N-isopropylacrylamide in toluene at −40°C in the presence of fourfold amounts of fluorinated alcohols was investigated. The 13C NMR analysis of the obtained polymers suggested that the addition of fluorinated alcohols induced heterotactic specificity in radical polymerization of NIPAAm, although syndiotactic poly(NIPAAm)s were obtained by adding alkyl alcohols as we have previously reported. To the best of our knowledge, this is the first synthesis of heterotactic poly(NIPAAm).
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subjects Applied sciences
Exact sciences and technology
Heterotactic polymer
N-Isopropylacrylamide
Organic polymers
Physicochemistry of polymers
Polymerization
Preparation, kinetics, thermodynamics, mechanism and catalysts
Radical polymerization
title Heterotactic poly(N-isopropylacrylamide) prepared via radical polymerization in the presence of fluorinated alcohols
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