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Poly(2-oxazoline)s Based on Phenolic Acids

  • A series of phenolic-acid-based 2-oxazoline monomers with methoxy-substituted phenyl and cinnamyl side chains is synthesized and polymerized in a microwave reactor at 140 °C using methyl tosylate as the initiator. The obtained poly(2-oxazoline)s are characterized by NMR spectroscopy, MALDI-TOF mass spectrometry, and size-exclusion chromatography (SEC). Kinetic studies reveal that the microwave-assisted polymerization is fast and completed within less than ≈10 min for low monomer-to-initiator ratios of ≤25. Polymers with number-average molar masses of up to 6500 g mol−1 and low dispersity (1.2–1.3) are produced. The aryl methyl ethers are successfully cleaved with aluminum triiodide/N,N′-diisopropylcarbodiimide to give a poly(2-oxazoline) with pendent catechol groups.

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Metadaten
Author details:Nils Lüdecke, Steffen M. Weidner, Helmut SchlaadORCiDGND
DOI:https://doi.org/10.1002/marc.201900404
ISSN:1022-1336
ISSN:1521-3927
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/31583798
Title of parent work (English):Macromolecular rapid communications
Publisher:Wiley-VCH
Place of publishing:Weinheim
Publication type:Article
Language:English
Date of first publication:2019/10/03
Publication year:2019
Release date:2021/06/03
Tag:2-oxazoline; catechol; cationic ring-opening polymerization; microwave; phenolic acid
Volume:41
Issue:1
Number of pages:5
Funding institution:University of Potsdam
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
DDC classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Peer review:Referiert
Publishing method:Open Access / Bronze Open-Access
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