Issue
Korean Journal of Chemical Engineering,
Vol.22, No.4, 556-559, 2005
Copolymerization of Phenyl Glycidyl Ether with Carbon Dioxide Catalyzed by Ionic Liquids
The copolymerization of phenyl glycidyl ether (PGE) and carbon dioxide was performed without any solvent in the presence of ionic liquid as catalyst. The reaction was carried out in a batch autoclave reactor. The carbonate content of polycarbonate was affected by the structure of imidazolium salt ionic liquid; the one with the cation of bulkier alkyl chain length and with more nucleophilic anion showed better reactivity. However, the yield of carbon dioxide addition decreased when hexyl or octyl containing ionic liquids were used in place of butyl group in 1-alkyl-3-methyl imidazolium salts. The carbonate content and turnover number (TON) of the polycarbonate increased as the reaction temperature increased from 40 to 80 oC. However, the carbonate content decreased with increasing reaction time.
[References]
  1. Aida T, Ishikawa M, Inoue S, Macromolecules, 19, 8, 1986
  2. Chen XH, Shen ZQ, Zhang YF, Macromolecules, 24, 5305, 1991
  3. Darensbourg DJ, Holtcamp MW, Coord. Chem. Rev., 153, 155, 1996
  4. Darensbourg DJ, Yarbrough JC, Ortiz C, Fang CC, J. Am. Chem. Soc., 125(25), 7586, 2003
  5. Inoue S, Tsuruta T, Koinuma H, J. Polym. Sci. Polym. Lett., 7, 287, 1969
  6. Olivier-Bourbigou H, Magna L, J. Mol. Catal. A-Chem., 182, 419, 2002
  7. Rokicki A, "Poly(alkylene carbonates) with Controlled Molecular Weight", US Patent 4,943, 677, 1990
  8. Rokicki A, Kuran WJ, J. Makromol. Sci. Rev. Mcromol. Chem., C21, 135, 1981
  9. Shin DH, Kim JJ, Yu BS, Lee MH, Park DW, Korean J. Chem. Eng., 20(1), 71, 2003
  10. Song CE, Shim WH, Roh EJ, Chio JH, Chem. Commun., 1695, 2000
  11. Super MS, Beckman EJ, Trends Polym. Sci., 5(7), 236, 1997
  12. Welton T, Chem. Rev., 99(8), 2071, 1999
  13. Yu BS, Jeong ES, Kim KH, Park DW, Park SW, Lee JW, React. Kinet. Catal. Lett., 84, 175, 2005