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Volumn 70, Issue , 2015, Pages 125-135

Poly(hydroxy urethane)s based on renewable diglycerol dicarbonate

Author keywords

Biobased; Diglycerol dicarbonate; Isocyanate free; NMR; Poly(hydroxy urethane); Thermal properties

Indexed keywords

ESTERS; FOURIER TRANSFORM INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; THERMODYNAMIC PROPERTIES;

EID: 84937574876     PISSN: 00143057     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.eurpolymj.2015.07.011     Document Type: Article
Times cited : (80)

References (38)
  • 1
    • 0001520765 scopus 로고
    • Das Di-Isocyanat-Polyadditionsverfahren (polyurethane)
    • O. Bayer Das Di-Isocyanat-Polyadditionsverfahren (polyurethane) Angew. Chem. 59 1947 257 272 10.1002/ange.19470590901
    • (1947) Angew. Chem. , vol.59 , pp. 257-272
    • Bayer, O.1
  • 3
    • 0027680650 scopus 로고
    • Synthesis and properties of poly(hydroxyurethane)s
    • N. Kihara, and T. Endo Synthesis and properties of poly(hydroxyurethane)s J. Polym. Sci. Part A: Polym. Chem. 31 1993 2765 2773 10.1002/pola.1993.080311113
    • (1993) J. Polym. Sci. Part A: Polym. Chem. , vol.31 , pp. 2765-2773
    • Kihara, N.1    Endo, T.2
  • 4
    • 4143096515 scopus 로고    scopus 로고
    • Synthesis and thermal properties of [n]-polyurethanes
    • S. Neffgen, J. Kušan, T. Fey, H. Keul, and H. Höcker Synthesis and thermal properties of [n]-polyurethanes Macromol. Chem. Phys. 201 2000 2108 2114 10.1002/1521-3935(20001101)201:16<2108::AID-MACP2108>3.0.CO;2-7
    • (2000) Macromol. Chem. Phys. , vol.201 , pp. 2108-2114
    • Neffgen, S.1    Kušan, J.2    Fey, T.3    Keul, H.4    Höcker, H.5
  • 5
    • 0032097552 scopus 로고    scopus 로고
    • Copolymerization of 2,2-dimethyltrimethylene carbonate with tetramethylene urea: a new route to the polyurethane
    • F. Schmitz, H. Keul, and H. Höcker Copolymerization of 2,2-dimethyltrimethylene carbonate with tetramethylene urea: a new route to the polyurethane Polymer (Guildf) 39 1998 3179 3186 10.1016/S0032-3861(97)00640-X
    • (1998) Polymer (Guildf) , vol.39 , pp. 3179-3186
    • Schmitz, F.1    Keul, H.2    Höcker, H.3
  • 6
    • 0033523639 scopus 로고    scopus 로고
    • [n]-Polyurethanes: synthesis and Characterization
    • R.M. Versteegen, R.P. Sijbesma, and E.W. Meijer [n]-Polyurethanes: synthesis and Characterization Angew. Chem. Int. Ed. Engl. 38 1999 2917 2919 10.1002/(SICI)1521-3773(19991004)38:19<2917::AID-ANIE2917>3.0.CO;2-7
    • (1999) Angew. Chem. Int. Ed. Engl. , vol.38 , pp. 2917-2919
    • Versteegen, R.M.1    Sijbesma, R.P.2    Meijer, E.W.3
  • 7
    • 1042279652 scopus 로고    scopus 로고
    • Synthesis of thermoresponsive polyurethane from 2-methylaziridine and supercritical carbon dioxide
    • O. Ihata, Y. Kayaki, and T. Ikariya Synthesis of thermoresponsive polyurethane from 2-methylaziridine and supercritical carbon dioxide Angew. Chem. Int. Ed. Engl. 43 2004 717 719 10.1002/anie.200352215
    • (2004) Angew. Chem. Int. Ed. Engl. , vol.43 , pp. 717-719
    • Ihata, O.1    Kayaki, Y.2    Ikariya, T.3
  • 9
    • 84941066077 scopus 로고    scopus 로고
    • Quantitative synthesis of bis(cyclic carbonate)s by iron catalyst for non-isocyanate polyurethane synthesis
    • X. Sheng, G. Ren, Y. Qin, X. Chen, X. Wang, and F. Wang Quantitative synthesis of bis(cyclic carbonate)s by iron catalyst for non-isocyanate polyurethane synthesis Green Chem. 17 2015 373 379 10.1039/C4GC01294A
    • (2015) Green Chem. , vol.17 , pp. 373-379
    • Sheng, X.1    Ren, G.2    Qin, Y.3    Chen, X.4    Wang, X.5    Wang, F.6
  • 10
    • 84902995530 scopus 로고    scopus 로고
    • Novel green fatty acid-based bis-cyclic carbonates for the synthesis of isocyanate-free poly(hydroxyurethane amide)s
    • L. Maisonneuve, A.S. More, S. Foltran, C. Alfos, F. Robert, Y. Landais, and et al. Novel green fatty acid-based bis-cyclic carbonates for the synthesis of isocyanate-free poly(hydroxyurethane amide)s RSC Adv. 4 2014 25795 25803 10.1039/c4ra03675a
    • (2014) RSC Adv. , vol.4 , pp. 25795-25803
    • Maisonneuve, L.1    More, A.S.2    Foltran, S.3    Alfos, C.4    Robert, F.5    Landais, Y.6
  • 11
    • 84861222637 scopus 로고    scopus 로고
    • Optimization of the synthesis of polyhydroxyurethanes using dynamic rheometry
    • S. Benyahya, B. Boutevin, S. Caillol, V. Lapinte, and J.-P. Habas Optimization of the synthesis of polyhydroxyurethanes using dynamic rheometry Polym. Int. 61 2012 918 925 10.1002/pi.4159
    • (2012) Polym. Int. , vol.61 , pp. 918-925
    • Benyahya, S.1    Boutevin, B.2    Caillol, S.3    Lapinte, V.4    Habas, J.-P.5
  • 12
    • 84860485268 scopus 로고    scopus 로고
    • Cyclic limonene dicarbonate as a new monomer for non-isocyanate oligo- and polyurethanes (NIPU) based upon terpenes
    • M. Bähr, A. Bitto, and R. Mülhaupt Cyclic limonene dicarbonate as a new monomer for non-isocyanate oligo- and polyurethanes (NIPU) based upon terpenes Green Chem. 14 2012 1447 1454 10.1039/c2gc35099h
    • (2012) Green Chem. , vol.14 , pp. 1447-1454
    • Bähr, M.1    Bitto, A.2    Mülhaupt, R.3
  • 13
    • 84908429130 scopus 로고    scopus 로고
    • Original biobased nonisocyanate polyurethanes: solvent- and catalyst-free synthesis, thermal properties and rheological behaviour
    • C. Carré, L. Bonnet, and L. Avérous Original biobased nonisocyanate polyurethanes: solvent- and catalyst-free synthesis, thermal properties and rheological behaviour RSC Adv. 4 2014 54018 54025 10.1039/C4RA09794G
    • (2014) RSC Adv. , vol.4 , pp. 54018-54025
    • Carré, C.1    Bonnet, L.2    Avérous, L.3
  • 14
    • 84896951143 scopus 로고    scopus 로고
    • α,ω-Di(glycerol carbonate) telechelic polyesters and polyolefins as precursors to polyhydroxyurethanes: an isocyanate-free approach
    • L. Annunziata, A.K. Diallo, S. Fouquay, G. Michaud, F. Simon, J.-M. Brusson, and et al. α,ω-Di(glycerol carbonate) telechelic polyesters and polyolefins as precursors to polyhydroxyurethanes: an isocyanate-free approach Green Chem. 16 2014 1947 1956 10.1039/c3gc41821a
    • (2014) Green Chem. , vol.16 , pp. 1947-1956
    • Annunziata, L.1    Diallo, A.K.2    Fouquay, S.3    Michaud, G.4    Simon, F.5    Brusson, J.-M.6
  • 15
    • 0033718936 scopus 로고    scopus 로고
    • Addition of five-membered cyclic carbonate with amine and its application to polymer synthesis
    • A. Steblyanko, W. Choi, F. Sanda, and T. Endo Addition of five-membered cyclic carbonate with amine and its application to polymer synthesis J. Polym. Sci. Part A: Polym. Chem. 38 2000 2375 2380 10.1002/1099-0518(20000701)38:13<2375::AID-POLA100>3.0.CO;2-U
    • (2000) J. Polym. Sci. Part A: Polym. Chem. , vol.38 , pp. 2375-2380
    • Steblyanko, A.1    Choi, W.2    Sanda, F.3    Endo, T.4
  • 16
    • 0035281170 scopus 로고    scopus 로고
    • Structural analysis of polyhydroxyurethane obtained by polyaddition of bifunctional five-membered cyclic carbonate and diamine based on the model reaction
    • H. Tomita, F. Sanda, and T. Endo Structural analysis of polyhydroxyurethane obtained by polyaddition of bifunctional five-membered cyclic carbonate and diamine based on the model reaction J. Polym. Sci. Part A: Polym. Chem. 39 2001 851 859 10.1002/1099-0518(20010315)39:6<851::AID-POLA1058>3.0.CO;2-3
    • (2001) J. Polym. Sci. Part A: Polym. Chem. , vol.39 , pp. 851-859
    • Tomita, H.1    Sanda, F.2    Endo, T.3
  • 17
    • 27744493688 scopus 로고    scopus 로고
    • Nucleophilic polyaddition in water based on chemo-selective reaction of cyclic carbonate with amine
    • B. Ochiai, Y. Satoh, and T. Endo Nucleophilic polyaddition in water based on chemo-selective reaction of cyclic carbonate with amine Green Chem. 7 2005 765 767 10.1039/b511019j
    • (2005) Green Chem. , vol.7 , pp. 765-767
    • Ochiai, B.1    Satoh, Y.2    Endo, T.3
  • 18
    • 0035576964 scopus 로고    scopus 로고
    • Polyaddition of bis(seven-membered cyclic carbonate) with diamines: a novel and efficient synthetic method for polyhydroxyurethanes
    • H. Tomita, F. Sanda, and T. Endo Polyaddition of bis(seven-membered cyclic carbonate) with diamines: a novel and efficient synthetic method for polyhydroxyurethanes J. Polym. Sci. Part A: Polym. Chem. 39 2001 4091 4100 10.1002/pola.10058
    • (2001) J. Polym. Sci. Part A: Polym. Chem. , vol.39 , pp. 4091-4100
    • Tomita, H.1    Sanda, F.2    Endo, T.3
  • 19
    • 0035281183 scopus 로고    scopus 로고
    • Polyaddition behavior of bis(five- and six-membered cyclic carbonate)s with diamine
    • H. Tomita, F. Sanda, and T. Endo Polyaddition behavior of bis(five- and six-membered cyclic carbonate)s with diamine J. Polym. Sci. Part A: Polym. Chem. 39 2001 860 867 10.1002/1099-0518(20010315)39:6<860::AID-POLA1059>3.0.CO;2-2
    • (2001) J. Polym. Sci. Part A: Polym. Chem. , vol.39 , pp. 860-867
    • Tomita, H.1    Sanda, F.2    Endo, T.3
  • 20
    • 79751523703 scopus 로고    scopus 로고
    • Poly(carbonate-urethane): an isocyanate-free procedure from α,ω-di(cyclic carbonate) telechelic poly(trimethylene carbonate)s
    • M. Helou, J.-F. Carpentier, and S.M. Guillaume Poly(carbonate-urethane): an isocyanate-free procedure from α,ω-di(cyclic carbonate) telechelic poly(trimethylene carbonate)s Green Chem. 13 2011 266 271 10.1039/c0gc00686f
    • (2011) Green Chem. , vol.13 , pp. 266-271
    • Helou, M.1    Carpentier, J.-F.2    Guillaume, S.M.3
  • 21
    • 80055085259 scopus 로고    scopus 로고
    • Synthesis and characterization of polyhydroxyurethanes prepared from difunctional six-membered ring carbonates
    • T. Anders, H. Keul, and M. Möller Synthesis and characterization of polyhydroxyurethanes prepared from difunctional six-membered ring carbonates Des. Monomers Polym. 14 2011 593 608 10.1163/156855511X601592
    • (2011) Des. Monomers Polym. , vol.14 , pp. 593-608
    • Anders, T.1    Keul, H.2    Möller, M.3
  • 22
    • 80054024034 scopus 로고    scopus 로고
    • Synthesis of glycerin carbonate-based intermediates using thiol-ene chemistry and isocyanate free polyhydroxyurethanes therefrom
    • S. Benyahya, M. Desroches, R. Auvergne, S. Carlotti, S. Caillol, and B. Boutevin Synthesis of glycerin carbonate-based intermediates using thiol-ene chemistry and isocyanate free polyhydroxyurethanes therefrom Polym. Chem. 2 2011 2661 2667 10.1039/c1py00289a
    • (2011) Polym. Chem. , vol.2 , pp. 2661-2667
    • Benyahya, S.1    Desroches, M.2    Auvergne, R.3    Carlotti, S.4    Caillol, S.5    Boutevin, B.6
  • 24
    • 38549149213 scopus 로고    scopus 로고
    • Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals
    • C.-H. Zhou, J.N. Beltramini, Y.-X. Fan, and G.Q. Lu Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals Chem. Soc. Rev. 37 2008 527 549 10.1039/b707343g
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 527-549
    • Zhou, C.-H.1    Beltramini, J.N.2    Fan, Y.-X.3    Lu, G.Q.4
  • 25
    • 34447129755 scopus 로고    scopus 로고
    • Chemical routes for the transformation of biomass into chemicals
    • A. Corma, S. Iborra, and A. Velty Chemical routes for the transformation of biomass into chemicals Chem. Rev. 107 2007 2411 2502 10.1021/cr050989d
    • (2007) Chem. Rev. , vol.107 , pp. 2411-2502
    • Corma, A.1    Iborra, S.2    Velty, A.3
  • 26
    • 33749465605 scopus 로고    scopus 로고
    • Dehydration of glycerol to acetol via catalytic reactive distillation
    • C.-W. Chiu, M.A. Dasari, G.J. Suppes, and W.R. Sutterlin Dehydration of glycerol to acetol via catalytic reactive distillation AIChE J. 52 2006 3543 3548 10.1002/aic.10951
    • (2006) AIChE J. , vol.52 , pp. 3543-3548
    • Chiu, C.-W.1    Dasari, M.A.2    Suppes, G.J.3    Sutterlin, W.R.4
  • 27
    • 76249085645 scopus 로고    scopus 로고
    • Acid-catalyzed oligomerization of glycerol investigated by electrospray ionization mass spectrometry
    • M.A. Medeiros, M.H. Araujo, R. Augusti, L.C.A. de Oliveira, and R.M. Lago Acid-catalyzed oligomerization of glycerol investigated by electrospray ionization mass spectrometry J. Braz. Chem. Soc. 20 2009 1667 1673 10.1590/S0103-50532009000900015
    • (2009) J. Braz. Chem. Soc. , vol.20 , pp. 1667-1673
    • Medeiros, M.A.1    Araujo, M.H.2    Augusti, R.3    De Oliveira, L.C.A.4    Lago, R.M.5
  • 28
    • 84923105716 scopus 로고    scopus 로고
    • Diglycerol-based polyesters: melt polymerization with hydrophobic anhydrides
    • D. Dakshinamoorthy, A.K. Weinstock, K. Damodaran, D.F. Iwig, and R.T. Mathers Diglycerol-based polyesters: melt polymerization with hydrophobic anhydrides ChemSusChem 7 2014 2923 2929 10.1002/cssc.201402249
    • (2014) ChemSusChem , vol.7 , pp. 2923-2929
    • Dakshinamoorthy, D.1    Weinstock, A.K.2    Damodaran, K.3    Iwig, D.F.4    Mathers, R.T.5
  • 29
    • 84928495877 scopus 로고    scopus 로고
    • Recent advances in glycerol polymers: chemistry and biomedical applications
    • H. Zhang, and M.W. Grinstaff Recent advances in glycerol polymers: chemistry and biomedical applications Macromol. Rapid Commun. 35 2014 1906 1924 10.1002/marc.201400389
    • (2014) Macromol. Rapid Commun. , vol.35 , pp. 1906-1924
    • Zhang, H.1    Grinstaff, M.W.2
  • 32
    • 84941802157 scopus 로고    scopus 로고
    • Reusable Mg-Al hydrotalcites for the catalytic synthesis of diglycerol dicarbonate from diglycerol and dimethyl carbonate
    • J.A. Stewart, B.M. Weckhuysen, and P.C.A. Bruijnincx Reusable Mg-Al hydrotalcites for the catalytic synthesis of diglycerol dicarbonate from diglycerol and dimethyl carbonate Catal. Today 2014 10.1016/j.cattod.2014.06.035
    • (2014) Catal. Today
    • Stewart, J.A.1    Weckhuysen, B.M.2    Bruijnincx, P.C.A.3
  • 33
    • 83455228406 scopus 로고    scopus 로고
    • Renewable rigid diamines: efficient, stereospecific synthesis of high purity isohexide diamines
    • S. Thiyagarajan, L. Gootjes, W. Vogelzang, J. van Haveren, M. Lutz, and D.S. van Es Renewable rigid diamines: efficient, stereospecific synthesis of high purity isohexide diamines ChemSusChem 4 2011 1823 1829 10.1002/cssc.201100398
    • (2011) ChemSusChem , vol.4 , pp. 1823-1829
    • Thiyagarajan, S.1    Gootjes, L.2    Vogelzang, W.3    Van Haveren, J.4    Lutz, M.5    Van Es, D.S.6
  • 34
    • 78650170971 scopus 로고    scopus 로고
    • Chiral building blocks from biomass: 2,5-diamino-2,5-dideoxy-1,4-3,6-dianhydroiditol
    • S. Thiyagarajan, L. Gootjes, W. Vogelzang, J. Wu, J. van Haveren, and D.S. van Es Chiral building blocks from biomass: 2,5-diamino-2,5-dideoxy-1,4-3,6-dianhydroiditol Tetrahedron 67 2011 383 389 10.1016/j.tet.2010.11.031
    • (2011) Tetrahedron , vol.67 , pp. 383-389
    • Thiyagarajan, S.1    Gootjes, L.2    Vogelzang, W.3    Wu, J.4    Van Haveren, J.5    Van Es, D.S.6
  • 35
    • 84857153508 scopus 로고    scopus 로고
    • Linseed and soybean oil-based polyurethanes prepared via the non-isocyanate route and catalytic carbon dioxide conversion
    • M. Bähr, and R. Mülhaupt Linseed and soybean oil-based polyurethanes prepared via the non-isocyanate route and catalytic carbon dioxide conversion Green Chem. 14 2012 483 489 10.1039/c2gc16230j
    • (2012) Green Chem. , vol.14 , pp. 483-489
    • Bähr, M.1    Mülhaupt, R.2
  • 37
    • 84892153884 scopus 로고    scopus 로고
    • Chain extension of dimer fatty acid- and sugar-based polyurethanes in aqueous dispersions
    • Y. Li, B.A.J. Noordover, R.A.T.M. van Benthem, and C.E. Koning Chain extension of dimer fatty acid- and sugar-based polyurethanes in aqueous dispersions Eur. Polym. J. 52 2014 12 22 10.1016/j.eurpolymj.2013.12.007
    • (2014) Eur. Polym. J. , vol.52 , pp. 12-22
    • Li, Y.1    Noordover, B.A.J.2    Van Benthem, R.A.T.M.3    Koning, C.E.4
  • 38
    • 84905384189 scopus 로고    scopus 로고
    • Property profile of poly(urethane urea) dispersions containing dimer fatty acid-, sugar- and amino acid-based building blocks
    • Y. Li, B.A.J. Noordover, R.A.T.M. van Benthem, and C.E. Koning Property profile of poly(urethane urea) dispersions containing dimer fatty acid-, sugar- and amino acid-based building blocks Eur. Polym. J. 59 2014 8 18 10.1016/j.eurpolymj.2014.06.016
    • (2014) Eur. Polym. J. , vol.59 , pp. 8-18
    • Li, Y.1    Noordover, B.A.J.2    Van Benthem, R.A.T.M.3    Koning, C.E.4


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