화학공학소재연구정보센터
Macromolecular Research, Vol.27, No.9, 895-904, September, 2019
Thermally Healable Polyurethanes Based on Furfural-Derived Monomers via Baylis-Hillman Reaction
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Two novel acrylate monomers with diol group, 2-hydroxyethyl 2-(furan-2-yl(hydroxy)methyl)acrylate and methyl 2-(hydroxy(5-(hydroxymethyl)furan-2-yl)methyl)acrylate, were synthesized via Baylis-Hillman reaction in moderate yields. The monomer 2-hydroxyethyl 2-(furan-2-yl(hydroxy)methyl)acrylate was obtained from furfural and 2-hydroxyethyl acrylate (HEA); methyl 2-(hydroxy[5-(hydroxymethyl)furan-2-yl)methyl)acrylate was prepared from 5-hydroxymethl furfural (HMF) and methyl acrylate. The monomer 2-hydroxyethyl 2-(furan-2-yl(hydroxy)methyl)acrylate reacted with toluene diisocyanate (TDI)-derived or hexamethylene diisocyanate (HDI)-derived diisocyanate oligomers to obtain the corresponding linear polyurethane oligmers PU-1T and PU-1H. Similarly, the diol methyl 2-(hydroxy(5-(hydroxymethyl)furan-2-yl)methyl)acrylate reacted with TDI- or HDI-derived diisocyanate oligomers to obtain the corresponding linear polyurethane oligmers PU-2T and PU-2H. The number-average molecular weights of the linear polyurethane oligomers are approximately 300-350 Da. There are furan groups in the linear polyurethane oligomers PU-1T, PU-1H, PU-2T and PU-2H, which makes them capable of undergoing reversible Diels-Alder reaction with 4,4′-bismaleimidodiphenylmethane (BMI) to form the corresponding crosslinked polyurethanes CPU-1T, CPU-1H, CPU-2T and CPU-2H. Pencil hardness of CPU-1T, CPU-1H, CPU-2T and CPU-2H are 3H, 2H, 2H and HB, respectively. Glass transition temperatures of CPU-1T, CPU-1H, CPU-2T and CPU-2H are 104.8, 97.6, 5.1 and 1.2 °C, respectively. TGA analysis shows that Td90 values of the CPUs range from 180 to 250 °C. Furthermore, the reversible crosslinked polyurethanes CPU-1T and CPU-1H can be completely self-healed at 90 °C for 3 h, while CPU-2T and CPU-2H can self-heal at 80 °C for 3 h presumably due to their low glass transition temperatures.
  1. Zhang PF, Li GQ, Prog. Polym. Sci, 57, 32 (2016)
  2. Taylor DL, Panhuis MIH, Adv. Mater., 28(41), 9060 (2016)
  3. An SY, Arunbabu D, Noh SM, Song YK, Oh JK, Chem. Commun., 51, 13058 (2015)
  4. Chen YJ, Diaz-Dussan D, Wu D, Wang WD, Peng YY, Asha AB, Hall DG, Ishihara K, Narain R, ACS Macro Lett., 7, 904 (2018)
  5. Peng HJ, Huang JQ, Liu XY, Cheng XB, Xu WT, Zhao CZ, Wei F, Zhang Q, J. Am. Chem. Soc., 139(25), 8458 (2017)
  6. Chen YX, Xia C, Shepard Z, Smith N, Rice N, Peterson AM, Sakulich A, ACS Sustainable Chem. Eng., 5, 3955 (2017)
  7. White SR, Moore JS, Sottos NR, Krull BP, Cruz WAS, Gergely RCR, Science, 344(6184), 620 (2014)
  8. Li Y, Li L, Sun JQ, Angew. Chem.-Int. Edit., 49, 6129 (2010)
  9. Amaral AJR, Pasparakis G, Polym. Chem., 8, 6464 (2017)
  10. Diesendruck CE, Sottos NR, Moore JS, White SR, Angew. Chem.-Int. Edit., 54, 10428 (2015)
  11. Cheng CJ, Zhang X, Chen XH, Li J, Huang QH, Hu ZY, Tu YM, J. Polym. Res., 23, Article No. 110 (2016).
  12. Xu WM, Rong MZ, Zhang MQ, J. Mater. Chem. A, 4, 10683 (2016)
  13. Fuhrmann A, Gostl R, Wendt R, Kotteritzsch J, Hager MD, Schubert US, Brademann-Jock K, Thunemann AF, Nochel U, Behl M, Hecht S, Nat. Commun., 7, 13623 (2016)
  14. Yanagisawa Y, Nan YL, Okuro K, Aida T, Science, 359(6371), 72 (2018)
  15. Deng GH, Li FY, Yu HX, Liu FY, Liu CY, Sun WX, Jiang HF, Chen YM, ACS Macro Lett., 1, 275 (2012)
  16. Miwa Y, Kurachi J, Kohbara Y, Kutsumizu S, Nat. Commun., 10, 1828 (2019)
  17. Huang WG, Besar K, Zhang Y, Yang SY, Wiedman G, Liu Y, Guo WM, Song J, Hemker K, Hristova K, Kymissis IJ, Katz HE, Adv. Funct. Mater., 25(24), 3745 (2015)
  18. Yoshie N, Saito S, Oya N, Polymer, 52(26), 6074 (2011)
  19. Shao CY, Wang M, Chang HL, Xu F, Yang J, ACS Sustainable Chem. Eng., 5, 6167 (2017)
  20. Hillmyer MA, Science, 358(6365), 868 (2017)
  21. Marion P, Bernela B, Piccirilli A, Estrine B, Patouillard N, Guilbotf J, Jerome F, Green Chem., 19, 4973 (2017)
  22. Iwata T, Angew. Chem.-Int. Edit., 54, 3210 (2015)
  23. Alagi P, Ghorpade R, Jang JH, Patil C, Jirimali H, Gite V, Hong SC, Macromol. Res., 26(8), 696 (2018)
  24. Peleteiro S, Rivas S, Alonso JL, Santos V, Parajo JC, Bioresour. Technol., 202, 181 (2016)
  25. van Putten RJ, van der Waal JC, de Jong E, Rasrendra CB, Heeres HJ, de Vries JG, Chem. Rev., 113(3), 1499 (2013)
  26. Papageorgiou GZ, Tsanaktsis V, Papageorgiou DG, Exarhopoulos S, Papageorgiou M, Bikiaris DN, Polymer, 55(16), 3846 (2014)
  27. Wilson J, Chen EYX, ACS Sustain. Chem. Eng., 4, 4927 (2016)
  28. Wang JG, Liu XQ, Zhang YJ, Liu F, Zhu J, Polymer, 103, 1 (2016)
  29. Li XD, Jia P, Wang TF, ACS Catal., 6, 7621 (2016)
  30. Rajendran S, Raghunathan R, Hevus I, Krishnan R, Ugrinov A, Sibi MP, Webster DC, Sivaguru J, Angew. Chem.-Int. Edit., 54, 1159 (2015)
  31. Xu ZW, Yan PF, Liu KR, Wan L, Xu WJ, Li HX, Liu XM, Zhang ZC, ChemSusChem, 9, 1255 (2016)
  32. Kempe K, Krieg A, Becer CR, Schubert US, Chem. Soc. Rev., 41, 176 (2012)
  33. He BZ, Su HF, Bai TW, Wu YW, Li SW, Gao M, Hu RR, Zhao ZJ, Qin AJ, Ling J, Tang BZ, J. Am. Chem. Soc., 139(15), 5437 (2017)
  34. Yamago S, Nakamura Y, Polymer, 54(3), 981 (2013)
  35. Matyjaszewski K, Tsarevsky NV, J. Am. Chem. Soc., 136(18), 6513 (2014)
  36. Tuten BT, Bloesser FR, Marshall DL, Michalek L, Schmitt CW, Blanksby SJ, Barner-Kowollik C, ACS Macro Lett., 7, 898 (2018)
  37. Zhao Y, Wu HB, Wang ZL, Wei Y, Wang ZM, Tao L, Sci. Chin. Chem., 59, 1541 (2016)
  38. Xue HD, Zhao Y, Wu HB, Wang ZL, Yang B, Wei Y, Wang ZM, Tao L, J. Am. Chem. Soc., 138(28), 8690 (2016)
  39. Liu W, Luo X, Bao Y, Liu YP, Ning GH, Abdelwahab I, Li L, Nai CT, Hu ZG, Zhao D, Liu B, Quek SY, Loh KP, Nat. Chem., 9, 563 (2017)
  40. Wang XC, Wang K, Wang MF, Polym. Chem., 6, 1846 (2015)
  41. Basavaiah D, Veeraraghavaiah G, Chem. Soc. Rev., 41, 68 (2012)
  42. Bharadwaj KC, RSC Adv., 5, 75923 (2015)
  43. Basavaiah D, Reddy BS, Badsara SS, Chem. Rev., 110(9), 5447 (2010)
  44. Basavaiah D, Pal S, Veeraraghavaiah G, Bharadwaj KC, Tetrahedron, 71, 4659 (2015)
  45. Peng C, Joy A, Macromolecules, 47(4), 1258 (2014)
  46. Peng C, Joy A, J. Polym. Sci. A: Polym. Chem., 53(15), 1743 (2015)
  47. Baidya M, Kobayashi S, Brotzel F, Schmidhammer U, Riedle E, Mayr H, Angew. Chem.-Int. Edit., 46, 6176 (2007)
  48. Barthel MJ, Rudolph T, Teichler A, Paulus RM, Vitz J, Hoeppener S, Hager MD, Schacher FH, Schubert US, Adv. Funct. Mater., 23(39), 4921 (2013)
  49. Sheridan RJ, Bowman CN, Polym. Chem., 4, 4974 (2013)