Organocatalytic synthesis of novel renewable non‐isocyanate polyhydroxyurethanes |
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Authors: | Charlotte Duval Nasreddine Kébir Raphaël Jauseau Fabrice Burel |
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Institution: | INSA De Rouen Laboratoire PBS, UMR CNRS 6270 and FR 3038, Avenue De L'université, Normandie Université, France |
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Abstract: | Novel fully renewable AA‐BB type non‐isocyanate polyhydroxyurethanes were synthesized by the classical reaction between a diamine and a dicyclocarbonate. Sebacic acid was first reacted with an excess of glycerol carbonate, in presence of DCC and DMPA, leading to a renewable dicyclocarbonate monomer. Then, this monomer was reacted with several renewable diamines, in presence of 1,5,7‐triazabicyclo4.4.0]dec‐5‐ene (TBD), as organocatalyst, to afford linear and branched polymers. The obtained materials exhibited Tg values varied from ?27 to ?8 °C, Tm values varying from 100 to 165 °C, and thermal stabilities above 200 °C. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 758–764 |
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Keywords: | polyhydroxyurethanes NIPUs glycerol carbonate sebacic acid TBD |
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