DOI QR코드

DOI QR Code

Synthesis and Properties of Phenylene-containing Copolymer via the Catalytic Heck Coupling Reaction of Dipropargyl Group and Terphenyl Group

  • Koo, Bon Kweon ;
  • Lee, Sang Gu
  • Received : 2017.06.28
  • Accepted : 2017.08.03
  • Published : 2017.10.20

Abstract

Keywords

Terphenyl;Photoluminescence;Quantum yield;Fluorene derivative;Cross-linking

References

  1. Ito, T.; Shirakawa H.; Ikeda, S. J. Polym. Sci.: Part A: Polym. Chem. 1974, 12, 11. https://doi.org/10.1002/pol.1974.170120102
  2. Shirakawa, H.; Louis, E. J.; MacDiarmid, A. G.; Chiang, C. K.; Heeger, A. J. J. Chem. Soc. Chem. Commun. 1977, 16, 578.
  3. Chiang, C. K.; Fincher, C. R., Park, Y. W.; Heeger, A. J.; Shirakawa, H.; Louis, E. J.; Gau, S. C.; MacDiarmid, A. G. Phys. Rev. Lett. 1977, 39, 1098. https://doi.org/10.1103/PhysRevLett.39.1098
  4. Choi, S. K.; Gal, Y. S.; Jin, S. H.; Kim, H. K. Chem. Rev. 2000, 100, 1645. https://doi.org/10.1021/cr960080i
  5. Gal, Y. S.; Jin, S. H.; Park, J. W.; Lim, K. T. J. Ind. Eng. Chem. 2015, 30, 261. https://doi.org/10.1016/j.jiec.2015.05.031
  6. Liu, J.; Lam, J. W.Y.; Tang, B. Z. Chem. Rev. 2009, 109, 5799. https://doi.org/10.1021/cr900149d
  7. Siemsen, P.; Ivingston, R. C.; Diederich, F. Angew. Chem. Int. Ed. 2000, 39, 2632. https://doi.org/10.1002/1521-3773(20000804)39:15<2632::AID-ANIE2632>3.0.CO;2-F
  8. Stefani, H. A.; Guarezemini, A. S.; Cella, R. Tetrahedron 2010, 66, 7871. https://doi.org/10.1016/j.tet.2010.07.001
  9. Bredas, J. L.; Beljonne, D.; Coropceanu, V.; Cornil, J. Chem. Rev. 2004, 104, 4971. https://doi.org/10.1021/cr040084k
  10. Hoeben, F. J. M.; Jonkheijim, P.; Meijer, E. W.; Schenning, A. P. H. J. Chem. Rev. 2005, 105, 1491. https://doi.org/10.1021/cr030070z
  11. Jin, S. H.; Jang, M. S.; Suh, H. S.; Cho, H. N.; Lee, J. H.; Gal, Y. S. Chem. Mater. 2002, 14, 643. https://doi.org/10.1021/cm010593s
  12. Jin, S. H.; Gal, Y. S.; Cho, H. N. Mol. Cryst. Liq. Cryst. 2002, 377, 69. https://doi.org/10.1080/713738479
  13. Jin, S. H.; Kang, S. Y.; Yeom, I. S.; Kim, J. Y.; Park, S. H.; Lee, K.; Gal, Y. S.; Cho, H. N. Chem. Mater. 2002, 14, 5090. https://doi.org/10.1021/cm020610t
  14. Gal, Y. S.; Jin, S. H.; Choi, S. K. J. Mol. Cat. A: Chem. 2004, 213, 115. https://doi.org/10.1016/j.molcata.2003.10.055
  15. Kang, E. H.; Lee, I. S.; Choi, T. L. J. Am. Chem. Soc. 2011, 133, 11904. https://doi.org/10.1021/ja204309d
  16. Jin, S. H.; Kim, S. H.; Gal, Y. S. J. Polym. Sci.: Part A: Polym. Chem. 2001, 39, 4025. https://doi.org/10.1002/pola.10044
  17. Bunz, U. H. F. Chem. Rev. 2000, 100, 1605. https://doi.org/10.1021/cr990257j
  18. Nielsen, M. B.; Diederich, F. Chem. Rev. 2005, 105, 1837. https://doi.org/10.1021/cr9903353
  19. Lee, S. G.; Kwak, Y. W.; Park, J. W.; Jin, S. H.; Gal, Y. S. Curr. Appl. Phys. 2005, 5, 59. https://doi.org/10.1016/j.cap.2003.11.080
  20. Lee, S. G.; Kwak, Y. W.; Koo, B. K.; Jin, S. H.; Gal, Y. S. Mol. Cryst. Liq. Cryst. 2006, 458, 237. https://doi.org/10.1080/15421400600932421
  21. Lee, S. G.; Koo, B. K.; Gal, Y. S.; Kwak, Y. W. Mol. Cryst. Liq. Cryst. 2009, 498, 222. https://doi.org/10.1080/15421400802618950
  22. Lee, G. Y.; Gal, Y. S.; Lee, S. G. Mol. Cryst. Liq. Cryst. 2014, 597, 95. https://doi.org/10.1080/15421406.2014.932239
  23. Lee, G. Y.; Gal, Y. S.; Lee, S. G. Mol. Cryst. Liq. Cryst. 2016, 635, 167. https://doi.org/10.1080/15421406.2016.1200925

Acknowledgement

Supported by : Daegu Catholic University