Journal
GREEN CHEMISTRY
Volume 25, Issue 16, Pages 6200-6206Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3gc01779f
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Citric acid can form a cyclic imide when combined with a primary amine. By reacting a reduced derivative of citric acid with glycine, a cyclic imide diacid can be obtained. This monomer can be copolymerized with various diols to produce copolymers with adjustable glass transition temperature from 25 to 134°C. These polyimide-esters can hydrolyze under environmentally-relevant conditions, making them potential sustainable replacements for high Tg commodity plastics.
Citric acid is an abundant, naturally occurring small molecule that affords a cyclic imide when condensed with a primary amine. The reaction of a reduced derivative of citric acid and glycine yields a cyclic imide diacid. This monomer was copolymerized with a variety of linear diols and sugar-derived diols, yielding copolymers with a tunable glass transition temperature ranging from T-g = 25 to 134 & DEG;C. Unlike most polyesters, these polyimide-esters hydrolyze under environmentally-relevant conditions and thus, show promise as sustainable replacements for high T-g commodity plastics.
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