Two alternative approaches to the Diels-Alder polymerization of tung oil

Lacerda, Talita M.; Carvalho, Antonio J. F.; Gandini, Alessandro

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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Two alternative approaches to the Diels-Alder polymerization of tung oil

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Author(s):	Lacerda, Talita M. ^{[1, 2]} ; Carvalho, Antonio J. F. ^[1] ; Gandini, Alessandro ^{[1, 2]} Total Authors: 3
Affiliation:	^[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP - Brazil ^[2] Univ Sao Paulo, Escola Engn Sao Carlos, BR-13566590 Sao Carlos, SP - Brazil Total Affiliations: 2
Document type:	Journal article
Source:	RSC ADVANCES; v. 4, n. 51, p. 26829-26837, 2014.
Web of Science Citations:	13
Abstract
Novel linear and crosslinked polymers from non-modified and modified tung oil are reported. These materials are based on the exploitation of the Diels-Alder reaction using, on the one hand, the dienic character of the three conjugated double bonds of tung oil and their susceptibility to react with a dienophile, and, on the other hand, the bulk reaction of furfuryl amine at the ester moieties of tung oil to produce three fatty acid furan amides, still bearing the three conjugated double bonds, and their linear polymerization with bismaleimides. (AU)

FAPESP's process:	12/00124-9 - Synthesis and thermal-reversible polymerization of macromonomers derived from vegetal oil and furan.
Grantee:	Talita Martins Lacerda
Support Opportunities:	Scholarships in Brazil - Post-Doctoral

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