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Thiol-yne Reaction of Alkyne-d erivatized Fatty Acids: Thiol-Reactive Linear Polyurethane

Rodolfo J. González-Paz, Gerard Lligadas*, Juan C. Ronda, Marina Galià, Virginia Cádiz
Analytical Chemistry and Organic Chemistry Department, Rovira i Virgili University, C/Marcel.lí Domingo s/n, 43007, Tarragona, Spain
* Corresponding Author:

Journal of Renewable Materials 2013, 1(3), 187-194. https://doi.org/10.7569/JRM.2013.634114

Received 13 February 2013; Accepted 23 March 2013;

Abstract

A thiol-reactive linear polyurethane was synthesized from a vinyl-sulphide-containing diol and a commercial diisocyanate. The diol was obtained from 10-undecynol, an alkyne-derivatized fatty compound, using hydrothiolation as a key reaction step. 10-Undecynol was prepared by reduction of 10-undecinoic acid methyl ester, which was prepared by successive bromation, dehydrobromination of the corresponding alkenic fatty acid. Solution and surface polymer modifi cation with a fl uorescent thiol was successful.

Keywords

Vegetable oils, click chemistry, polyurethanes, renewable resources

Cite This Article

González-Paz, R. J., Lligadas, G., Ronda, J. C., Galià, M., Cádiz, V. (2013). Thiol-yne Reaction of Alkyne-d erivatized Fatty Acids: Thiol-Reactive Linear Polyurethane. Journal of Renewable Materials, 1(3), 187–194.



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