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Main‐chain functionalization of poly(L‐lactide) with pendant unsaturations
Department of Fibre and Polymer Technology, Royal Institute of Technology, Stockholm, Sweden.ORCID iD: 0000-0002-5081-1835
Department of Fibre and Polymer Technology, Royal Institute of Technology, Stockholm, Sweden.
Department of Fibre and Polymer Technology, Royal Institute of Technology, Stockholm, Sweden.
2012 (English)In: Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, E-ISSN 1099-0518, Vol. 50, no 15, p. 3039-3045Article in journal (Refereed) Published
Abstract [en]

Main-chain-functionalized poly(L-lactide) (PLLA) with pendant unsaturations was synthesized through a one-pot postpolymerization procedure with the PLLA homopolymer as the starting material. The material was functionalized through α-hydrogen abstraction by a sterically hindered strong base, lithium diisopropylamide, followed by the addition of an acid chloride. Two different acid chlorides were examined, lauroyl chloride as a concept electrophile and oleoyl chloride to provide the pendant unsaturations. The semisolvated system, together with branching reactions from the alpha position of the acid chloride, yielded a high molar amount of the incorporated reactant in the material. The unsaturations were preserved under the chosen conditions and the material exhibited surfactant-like properties in blends with oleic acid and PLLA. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012

Place, publisher, year, edition, pages
John Wiley & Sons, 2012. Vol. 50, no 15, p. 3039-3045
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Polymer Chemistry
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URN: urn:nbn:se:liu:diva-207569DOI: 10.1002/pola.26084OAI: oai:DiVA.org:liu-207569DiVA, id: diva2:1896829
Available from: 2024-09-11 Created: 2024-09-11 Last updated: 2024-12-05Bibliographically approved

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Olsen, Peter

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