Controlled\nSynthesis of Bioderived Poly(limonene carbonate)–Oligolysine\nHybrid Macromolecules

A straightforward and stepwise functionalization of poly(limonene\ncarbonate) (PLC) was achieved through the use of thiol–ene\nclick chemistry introducing primary amine groups. These amines are\ninitiating points for <i>N</i>-carboxy anhydride (NCA) ring-opening\npolymerization (ROP) reactions, allowing us to modify the PLC backbone\nwith oligolysine fragments, thereby creating a polymer brush type\nmacromolecule. These newly prepared biohybrid structures show a clear\nhydrophilic behavior as evident from their physical behavior and contact\nangle measurements.

Publication Details

Journal
Figshare
Published
2024-09-19
DOI
https://doi.org/10.1021/acsmacrolett.4c00461.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Controlled\nSynthesis of Bioderived Poly(limonene carbonate)–Oligolysine\nHybrid Macromolecules

Figshare
Mycorrhizal Fungi and Plant Interactions
article

Controlled\nSynthesis of Bioderived Poly(limonene carbonate)–Oligolysine\nHybrid Macromolecules

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Abstract

A straightforward and stepwise functionalization of poly(limonene\ncarbonate) (PLC) was achieved through the use of thiol–ene\nclick chemistry introducing primary amine groups. These amines are\ninitiating points for <i>N</i>-carboxy anhydride (NCA) ring-opening\npolymerization (ROP) reactions, allowing us to modify the PLC backbone\nwith oligolysine fragments, thereby creating a polymer brush type\nmacromolecule. These newly prepared biohybrid structures show a clear\nhydrophilic behavior as evident from their physical behavior and contact\nangle measurements.

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Openalex Percentile: Top 61%
Mycorrhizal Fungi and Plant Interactions
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Controlled\nSynthesis of Bioderived Poly(limonene carbonate)–Oligolysine\nHybrid Macromolecules · Figshare (2024) | TGRS Research Map | TGRS