NDLI: The application of the Diels-Alder reaction to polymer syntheses based on furan/maleimide reversible couplings

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The application of the Diels-Alder reaction to polymer syntheses based on furan/maleimide reversible couplings

Content Provider	Scilit
Author	Gandini, Alessandro
Copyright Year	2005
Description	The furan heterocycle is a dienic reagent particularly suitable for the Diels-Alder reaction and maleimides represent a typical family of complementary reagents because of their strong dienophilic character. This paper reviews critically the studies devoted to the exploitation of the Diels Alder reaction between those moieties to synthesise macromolecular materials possessing different structures and properties. The most relevant approaches in this field are (i) polycondensation reactions calling upon A-A and B-B monomers and (ii) reversible cross-linking of linear polymers bearing pendant furan or maleimide moieties, based on the temperature sensitivity of the Diels-Alder equilibrium
Related Links	http://www.scielo.br/scielo.php?script=sci_pdf&pid=S0104-14282005000200007&lng=en&nrm=iso&tlng=en
ISSN	01041428
e-ISSN	16785169
DOI	10.1590/s0104-14282005000200007
Journal	Polímeros
Issue Number	2
Volume Number	15
Language	English
Publisher	FapUNIFESP (SciELO)
Publisher Date	2005-06-01
Access Restriction	Open
Subject Keyword	Polímeros Polymer Science Reaction To Polymer Reversible Couplings Syntheses Based Polymer Syntheses maleimide Reversible Diels Alder Alder Reaction
Content Type	Text
Resource Type	Article
Subject	Organic Chemistry Chemical Engineering

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