Bioinspired all‐polyester diblock copolymers made from poly(pentadecalactone) and poly(3,4‐ethylene furanoate): synthesis and polymer film properties
Abstract: Bio-based, fully degradable aliphatic-aromatic block copolymers are synthesized from ω-pentadecalatone and cyclic oligo(3,4-ethylene furanoate). In the first approach, the ring-opening polymerization of the cyclic oligo(3,4-ethylene furanoate) is initiated by a poly(pentadecalactone) macroinitiator with a terminal hydroxy group. The reaction temperatures of the melt polymerization are 210–230 °C due to the high melting points of the oligo(3,4-ethylene furanoate). Under these conditions, transesterification is observed. The blockiness of the reaction products depends on the reaction temperature and on the ratio of pentadecalactone to 3,4-ethylene furanoate repeat units, which is 50:50, 80:20, and 90:10. At lower temperatures and more pentadecalactone content, the blockiness is larger. The number average molar mass of the block copolymers remains smaller than 20 000 g mol−1. In the second approach, poly(pentadecalactone) is functionalized with an alkyne group, and the OH group of the oligo(3,4-ethylene furanoate) (molar mass 1900 g mol−1) is converted into an azide group. Connecting the two polymers in a copper-catalyzed 1,3-dipolar addition reaction (“click reaction”) yields block copolymers with a number average molar mass of 12 400 g mol−1. The mechanical properties of the polymer films are intermediate between those of the parent homopolymers
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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Macromolecular chemistry and physics. - 225, 14 (2024) , 2300445, ISSN: 1521-3935
- Ereignis
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Veröffentlichung
- (wo)
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Freiburg
- (wer)
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Universität
- (wann)
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2024
- Urheber
- DOI
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10.1002/macp.202300445
- URN
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urn:nbn:de:bsz:25-freidok-2580900
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:26 MESZ
Datenpartner
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Saar, Julia
- Lienkamp, Karen
- Universität
Entstanden
- 2024