Organocatalytic synthesis of novel renewable non‐isocyanate polyhydroxyurethanes
C Duval, N Kébir, R Jauseau… - Journal of Polymer …, 2016 - Wiley Online Library
Journal of Polymer Science Part A: Polymer Chemistry, 2016•Wiley Online Library
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‐triazabicyclo [4.4. 0] dec‐5‐ene (TBD), as
organocatalyst, to afford linear and branched polymers. The obtained materials exhibited Tg …
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‐triazabicyclo [4.4. 0] dec‐5‐ene (TBD), as
organocatalyst, to afford linear and branched polymers. The obtained materials exhibited Tg …
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‐triazabicyclo[4.4.0]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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