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  Synthesis of SET-LRP-induced galactoglucomannan-diblock copolymers

Dax, D., Xu, C., Langvik, O., Hemming, J., Backman, P., & Willfor, S. (2013). Synthesis of SET-LRP-induced galactoglucomannan-diblock copolymers. Journal of Polymer Science, Part A: Polymer Chemistry, 51(23), 5100-5110. doi:10.1002/pola.26942.

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Dax, Daniel1, Autor                 
Xu, CL, Autor
Langvik, O, Autor
Hemming, J, Autor
Backman, P, Autor
Willfor, S, Autor
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1External Organizations, ou_persistent22              

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 Zusammenfassung: Polysaccharides are biorenewable and biodegradable starting materials for the development of functional materials. The synthesis of a monofunctional macroinitiator for single electron transfer-living radical polymerization was successfully developed from a wood polysaccharide-O-acetyl galactoglucomannan (GGM) using a beforehand synthesized amino-functional -bromoisobutyryl derivative applying reductive amination. The GGM macroinitiator was employed to initiate a controlled radical polymerization of [2-(methacryloyloxy)ethyl]trimethylammonium chloride (MeDMA), methyl methacrylate (MMA), and N-isopropylacrylamide (NIPAM) using Cu-0/Me-6-Tren as a catalyst. The either charged or amphiphilic GGM-b-copolymers with different chain lengths of the synthetic block were successfully synthesized without prior hydrophobization of the GGM chain and dimethyl sulfoxide (DMSO) or DMSO/water mixtures were used as solvents. This novel synthetic approach may find untapped potentials particularly for the development of polysaccharide-based amphiphilic additives for cosmetics or paints and for the design of novel temperature or pH responsive polymers with such potential applications as in drug delivery systems or in biocomposites.

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 Datum: 2013
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1002/pola.26942
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Titel: Journal of Polymer Science, Part A: Polymer Chemistry
  Andere : J. Polym. Sci., Part A: Polym. Chem.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: New York, N.Y. : Wiley
Seiten: - Band / Heft: 51 (23) Artikelnummer: - Start- / Endseite: 5100 - 5110 Identifikator: ISSN: 0887-624X