Glycidyl ethers from acyclic terpenes: a versatile toolbox for multifunctional poly(ethylene glycol)s with modification opportunities

The synthesis of acyclic terpenyl glycidyl ethers (TGEs) and subsequent copolymerization with ethylene oxide (EO) via anionic ring-opening polymerization (AROP) are described. 1 H NMR in situ kinetics revealed the copolymer microstructures.

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Publication Details

Journal
Polymer Chemistry
Published
2024-12-06
DOI
https://doi.org/10.1039/d4py01201a
Citations
6
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
1.50
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article

Glycidyl ethers from acyclic terpenes: a versatile toolbox for multifunctional poly(ethylene glycol)s with modification opportunities

Holger Frey, Sandra Schüttner, Philipp Holzmüller, E. Hoffmann et al.
6 citations
Polymer Chemistry
Synthetic Organic Chemistry Methods
1.50
article

Glycidyl ethers from acyclic terpenes: a versatile toolbox for multifunctional poly(ethylene glycol)s with modification opportunities

Holger Frey, Sandra Schüttner, Philipp Holzmüller, E. Hoffmann, Gregor M. Linden
article en
6 citations

Abstract

The synthesis of acyclic terpenyl glycidyl ethers (TGEs) and subsequent copolymerization with ethylene oxide (EO) via anionic ring-opening polymerization (AROP) are described. 1 H NMR in situ kinetics revealed the copolymer microstructures.

Polymer ChemistryVol. 16(3)
Johannes Gutenberg University Mainz (DE)
Openalex Percentile: Top 18%
Synthetic Organic Chemistry Methods
1.50
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