Towards Thermally Reversible Networks Based on Furan-Functionalization of Jatropha Oil

A novel biobased monomer for the preparation of thermally reversible networks based on the Diels-Alder reaction was synthesized from jatropha oil. The oil was epoxidized and subsequently reacted with furfurylamine to attach furan groups via an epoxide ring opening reaction. However, furfurylamine al...

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Bibliographic Details
Published in:	Molecules (Basel, Switzerland) Vol. 25; no. 16; p. 3641
Main Authors:	Yuliati, Frita, Deuss, Peter J., Heeres, Hero J., Picchioni, Francesco
Format:	Journal Article
Language:	English
Published:	Switzerland MDPI AG 10.08.2020 MDPI
Subjects:	bismaleimide Bromides - chemistry Catalysis Cycloaddition Reaction Diels-Alder Epoxy Compounds - chemistry Epoxy resins experimental design Furans - chemistry furfurylamine Jatropha - chemistry Jatropha - metabolism jatropha oil Lithium Compounds - chemistry Plant Oils - chemistry Polymers Production capacity Raw materials Temperature Triglycerides - chemistry Vegetable oils experimental design furfurylamine Diels-Alder jatropha oil bismaleimide
ISSN:	1420-3049, 1420-3049
Online Access:	Get full text
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