Affiliation:
1. UMR 5253 CNRS-UM2-ENSCM-UM1, Institut Charles Gerhardt Montpellier, Equipe I.A.M., Montpellier, France
Abstract
This review proposes a platform approach for the synthesis of various building blocks from cardanol in one- or two-steps syntheses. Cardanol, which is a natural phenol, is issued from cashew nutshell liquid, a non-edible renewable resource, co-produced from the cashew industry in large commercial volumes. Cardanol is non-toxic and particularly suitable for the addition of aromatic renewable resources in polymers and materials. Various routes were used for the synthesis of di- and poly-functional building blocks used thereafter in polymer syntheses. Phenolation was used to dimerize/oligomerize cardanol in order to increase its functionality. Thio-ene was used to synthesize new reactive amines. Epoxidation and (meth)acrylation were also used to insert oxirane or (meth)acrylate groups in order to synthesize polymers and materials.
Subject
Materials Chemistry,Polymers and Plastics,Pollution
Cited by
18 articles.
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