Thiol-ene reaction followed by carbonate-amine reaction
July 8, 2014 14:50
Title: POLY(HYDROXYL URETHANE) COMPOSITIONS AND METHODS OF MAKING AND USING THE SAME
Number/Link: US20140182784
Applicant/Assignee: Inventors but with US goverment interest
Publication date: 3-07-2014
“Gist”: Crosslinked poly(hydroxyurethanes) are prepared by reacting a cyclic carbonate comprising a carbon-carbon double bond, a di-thiol and a polyamine.
Why it is interesting: According to this invention hydroxyurethanes are produced by first reacting a cyclic carbonate which has a double bond (e.g. 4-vinyl-1,3-dioxolan-2-one) with a dithiol (e.g. 1,6-hexanedithiol) using UV radiation and a UV initiator. The resulting di-carbonate is then reacted with a polyamine (e.g. diethylene triamine) resulting in a crosslinked poly(hydroxyurethane). Alternatively the carbonate-amine reaction can happen before the thiol-ene ‘click’ reaction. The materials can be used for binders and adhesives a.o. The reactions have the advantage of being solvent-, catalyst- and isocyanate-free and having a high yield.
Thiol-ene reaction followed by carbonate-amine reaction
Posted by Gerhard Bleys
Categories: Adhesives-Coatings
Tags: adhesives, binders, click chemistry, Environment, HNIPU, hybrid, isocyanate-free, NIPU, non-isocyanate polyurethane, thiol-ene reaction
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