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Synthesis of Star-like Polybutadienes by a Combination of Living Anionic Polymerization and “Click” Coupling Method 被引量:1

Synthesis of Star-like Polybutadienes by a Combination of Living Anionic Polymerization and “Click” Coupling Method
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摘要 Three-arm and four-arm star-like polybutadienes (PBds) were synthesized via the combination of living anionic polymerization and the click coupling method. Kinetic study showed that the click reaction between the azido group terminated PBd-t-N3 and the alkyne-containing multifunctional linking reagent was fast and highly efficient. All coupling reactions were fully accomplished within 40 min at 50 ℃ in toluene in the presence of the reducing agent Cu(0), proven by 1H-NMR, FTIR and GPC measurements. For the coupling reactions between the PBd-t-N3 polymer and dialkyne-containing compound, the final conversion of the coupled PBd-PBd polymer was ca. 97.0%. When a PBd-t-N3 polymer was reacted with trialkyne-containing or tetraalkyne-containing compound, the conversion of three-arm or four-arm PBd was around 95.5% or 87.0%, respectively. Several factors influencing the coupling efficiency were studied, including the molecular weight of the initial PBd-t-N3, arm numbers and the molar ratio of the azido group to the alkynyl group. The results indicated that the conversion of the target products would be promoted when the molecular weight of the PBd-t-N3 was low and the molar ratio of the azido to alkynyl groups was close to 1. Three-arm and four-arm star-like polybutadienes (PBds) were synthesized via the combination of living anionic polymerization and the click coupling method. Kinetic study showed that the click reaction between the azido group terminated PBd-t-N3 and the alkyne-containing multifunctional linking reagent was fast and highly efficient. All coupling reactions were fully accomplished within 40 min at 50 ℃ in toluene in the presence of the reducing agent Cu(0), proven by 1H-NMR, FTIR and GPC measurements. For the coupling reactions between the PBd-t-N3 polymer and dialkyne-containing compound, the final conversion of the coupled PBd-PBd polymer was ca. 97.0%. When a PBd-t-N3 polymer was reacted with trialkyne-containing or tetraalkyne-containing compound, the conversion of three-arm or four-arm PBd was around 95.5% or 87.0%, respectively. Several factors influencing the coupling efficiency were studied, including the molecular weight of the initial PBd-t-N3, arm numbers and the molar ratio of the azido group to the alkynyl group. The results indicated that the conversion of the target products would be promoted when the molecular weight of the PBd-t-N3 was low and the molar ratio of the azido to alkynyl groups was close to 1.
出处 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2014年第6期731-742,共12页 高分子科学(英文版)
基金 financially supported by the National Natural Science Foundation of China(Nos.51233005,21004060 and 51073149)
关键词 POLYBUTADIENE Living anionic polymerization Click chemistry Kinetic study Coupling efficiency Star-like. Polybutadiene Living anionic polymerization Click chemistry Kinetic study Coupling efficiency Star-like.
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  • 1Hadjichristidis, N., Pitsikalis, M., Pispas, S. and Iatrou, H., Chem. Rev., 2001, 101:3747.
  • 2Hadjichristidisa, N., Iatroua, H., Pitsikalisa, M. and Mays, J., Prog. Polym. Sci., 2006, 31:1068.
  • 3Khanna, K., Varshney, S. and Kakkar, A., Polym. Chem., 2010, 1 : 1171.
  • 4Kong, W., Li, B., Jin, Q., Ding, D. and Shi, A.C., J. Am. Chem. Soc., 2009, 131:8503.
  • 5Teng, J. and Zubarev, E.R., J. Am. Chem. Soc., 2003, 125:11840.
  • 6Gahleitner, M., Prog. Polym. Sci., 2001, 26:895.
  • 7Adams, C.H., Hutchings, L.R., Klein, P.G., McLeish, T.C.B. and Richards, R.W., Macromolecules, 1996, 29:5717.
  • 8Zelinski, R.P. and Wofford, C.F., J. Polym. Sci. Part A, 1965, 3:93.
  • 9Roovers, J. and Bywater S., Macromolecules, 1972, 5:384.
  • 10Roovers, J. and Bywater S., Macromolecules, 1974, 7:443.

同被引文献47

  • 1Koberstein J T. Molecular design of functional polymersurfaces[J]. Journal of Polymer Science Part B:PolymerPhysics,2004,42(16):2942–2956.
  • 2Wurm F,Klos J,R-der H J,et al. Synthesis and noncovalentprotein conjugation of linear-hyperbranched PEGpoly(glycerol)α,ωn-telechelics[J]. Journal of the AmericanChemical Society,2009,131(23):7954–7955.
  • 3Bouilhac C,Chirat M,Joly Duhamel C ‐ ,et al. Reverseiodine transfer polymerization(RITP)of 1,1,2,2-tetrahydroperfluorodecyl acrylate in supercritical carbondioxide[J]. Macromolecular Chemistry and Physics,2013,214(20):2259–2265.
  • 4David G,Boyer C,Tonnar J,et al. Use of iodocompoundsin radical polymerization[J]. Chemical Reviews,2006,106(9):3936-3962.
  • 5Vasile C. Handbook of Polyolefins[M]. 2nd ed. NewYork:Marcel Dekker,2000:249.
  • 6洪定-. 塑料工业手册:聚烯烃[M]. 北京:化学工业出版社,1999:296.
  • 7Chung T C. Synthesis of functional polyolefin copolymerswith graft and block structures[J]. Progress inPolymer Science,2002,27(1):39–85.
  • 8Povie G,Tran A T,Bonnaffé D,et al. Repairing the thiolenecoupling reaction[J]. Angewandte Chemie InternationalEdition,2014,53(15):3894–3898.
  • 9Franssen N M G,Reek J N H,de Bruin B. Synthesis offunctional ‘polyolefins’:State of the art and remainingchallenges[J]. Chemical Society Reviews ,2013 ,42(13):5809–5832.
  • 10Ziegler K. Aluminium-organische synthese im bereicholefinischer kohlenwasserstoffe[J]. Angewandte Chemie,1952,64(12):323–329.

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