Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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A Thiophene, Benzothiadiazole, and Carbazole-Based Copolymer : Synthesis and Characterization

  • Li, Ji-Cheng (Division of Chemical Engineering, Nanomaterials Processing Research Center, Chonbuk National University) ;
  • Meng, Qing Bo (Division of Chemical Engineering, Nanomaterials Processing Research Center, Chonbuk National University) ;
  • Kim, Jong-Seok (Division of Chemical Engineering, Nanomaterials Processing Research Center, Chonbuk National University) ;
  • Lee, Youn-Sik (Division of Chemical Engineering, Nanomaterials Processing Research Center, Chonbuk National University)
  • Published : 2009.04.20
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Abstract

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References

  1. Shaheen, S. E.; Brabec, C. J.; Sariciftci, N. S.; Padinger, F.; Fromherz, T.; Hummelen, J. C. Appl. Phys. Lett. 2001, 78, 841 https://doi.org/10.1063/1.1345834
  2. Padinger, F.; Rittberger, R.; Sariciftci, N. S. Adv. Funct. Mater. 2003, 13, 85 https://doi.org/10.1002/adfm.200390011
  3. Reyes-Reyes, M.; Kim, M.; Carroll, D. L. Appl. Phys. Lett. 2005, 87, 83506 https://doi.org/10.1063/1.2006986
  4. Ma, W.; Yang, C.; Gong, X.; Lee, K.; Heeger, A. J. Adv. Funct. Mater. 2005, 15, 1617 https://doi.org/10.1002/adfm.200500211
  5. Kim, J. Y.; Kim, S. H.; Lee, H.-H.; Lee, K.; Ma, W.; Gong, X.; Heeger, A. J. Adv. Mater. 2006, 18, 572 https://doi.org/10.1002/adma.200501825
  6. Boudreault, P.-L. T.; Michaud, A.; Leclerc, M. Macromol. Rapid Commun. 2007, 28, 2176 https://doi.org/10.1002/marc.200700470
  7. Akhtaruzzaman, M.; Tomura, M.; Nishida, J.; Yamashita, Y. J. Am. Chem. Soc. 1995, 117, 6791 https://doi.org/10.1021/ja00130a024
  8. Mullekom, H. A. M. V.; Vekemans, J. A. J. M.; Meijer, E. W. Chem. Eur. J. 1998, 4, 1235 https://doi.org/10.1002/(SICI)1521-3765(19980710)4:7<1235::AID-CHEM1235>3.0.CO;2-4
  9. Velusamy, M.; Thomas, K. R. J.; Lin, J. T.; Hsu, Y.; Ho, K. Org. Lett. 2005, 7, 1899 https://doi.org/10.1021/ol050417f
  10. He, Q.-G.; He, C.; Sun, Y.-X.; Wu, H.-X.; Li, Y.-F.; Bai, F.-L. Thin Solid Films 2008, 516, 5935 https://doi.org/10.1016/j.tsf.2007.10.058
  11. Peet, J.; Kim, J. Y.; Coates, N. E.; Ma, W. L.; Moses, D.; Heeger, A. J.; Bazan, G. C. Nat. Mater. 2007, 6, 497 https://doi.org/10.1038/nmat1928
  12. Yoonb, K. R.; Byuna, N. M.; Lee, H. S. Synth. Met. 2007, 157, 603 https://doi.org/10.1016/j.synthmet.2007.04.017
  13. Blouin, N.; Michaud, A.; Leclerc, M. Adv. Mater. 2007, 19, 2295 https://doi.org/10.1002/adma.200602496
  14. Li, J.-C.; Kim, S.-J.; Lee, S.-H.; Lee, Y.-S.; Zong, K. Macromol. Res. (2009), in press
  15. Zhu, Y.; Rabindranath, A. R.; Beyerlein, T.; Tieke, B. Macromolecules 2007, 40, 6981 https://doi.org/10.1021/ma0710941
  16. Moses, D.; Dogariu, A.; Heeger, A. J. Phy. Rev. B 2000, 61, 9373 https://doi.org/10.1103/PhysRevB.61.9373
  17. Thompson, B. C.; Kim, Y.-G.; McCarley, T. D.; Reynolds, J. R. J. Am. Chem. Soc. 2006, 128, 12714. https://doi.org/10.1021/ja061274a
  18. Hou, J. H.; Tan, Z. A.; Yan, Y.; He, Y. J.; Yang, C. H.; Li, Y. F. J. Am. Chem. Soc. 2006, 128, 4911 https://doi.org/10.1021/ja060141m
  19. Cremer, J.; B$\ddot(a)$uerle, P.; Wienk, M. M.; Janssen, R. A. J. Chem. Mater. 2006, 18, 5832 https://doi.org/10.1021/cm0620180
  20. Shi, C. J.; Yao, Y.; Yang, Y.; Pei, Q. B. J. Am. Chem. Soc. 2006, 128, 8980 https://doi.org/10.1021/ja061664x

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