Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Partially Ladder-Type Molecule-Based Donor-Acceptor Conjugated Oligomer: Synthesis and Properties

  • Poduval, Mithrabinda K.K. (Organic Material Synthesis Laboratory, Department of Chemistry, University of Incheon) ;
  • Hahn, So-Jung (Organic Material Synthesis Laboratory, Department of Chemistry, University of Incheon) ;
  • Kim, Tae-Hyun (Organic Material Synthesis Laboratory, Department of Chemistry, University of Incheon)
  • Received : 2012.02.09
  • Accepted : 2012.03.23
  • Published : 2012.06.20
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References

  1. Gunes, S.; Neugebauer, H.; Sariciftci, N. S. Chem. Rev. 2007, 107, 1324. https://doi.org/10.1021/cr050149z
  2. Scherf, U. J. Mater. Chem. 1999, 9, 1853. https://doi.org/10.1039/a900447e
  3. Scherf, U.; Müllen, K. Makromol. Chem. Rapid Commun. 1991, 12, 489. https://doi.org/10.1002/marc.1991.030120806
  4. Watson, M. D.; Fechtenkötter, A.; Müllen, K. Chem. Rev. 2001, 101, 1267.
  5. Agou, T.; Kobayashi, J.; Kawashima, T. Org. Lett. 2006, 8, 2241. https://doi.org/10.1021/ol060539n
  6. Xu, C.; Wakamiya, A.; Yamaguchi, S. J. Am. Chem. Soc. 2005, 127, 1638. https://doi.org/10.1021/ja042964m
  7. Mishra, A. K.; Graf, M.; Grasse, F.; Jacob, J.; List, R. J. W.; Müllen, K. Chem. Mater. 2006, 18, 2879. https://doi.org/10.1021/cm060072a
  8. Chen, Z.; Amara, J. P.; Thomas, S. W., III.; Swager, T. M. Macromolecules 2006, 39, 3202. https://doi.org/10.1021/ma052451f
  9. Jacob, J.; Sax, S.; Gaal, M.; List, E. J. W.; Grimsdale, A. C.; Müllen, K. Macromolecules 2005, 38, 9933. https://doi.org/10.1021/ma0517143
  10. Brown, A. R.; Pomp, A.; de Leeuw, D. M.; Klaassen, D. B. M.; Havinaga, E. E.; Herwig, P.; Mullen, K. J. Appl. Phys. 1996, 79, 2136. https://doi.org/10.1063/1.361071
  11. Herwig, P. T.; Mullen, K. Adv. Mater. 1999, 11, 480. https://doi.org/10.1002/(SICI)1521-4095(199904)11:6<480::AID-ADMA480>3.0.CO;2-U
  12. Vets, N.; Smet, M.; Dehaen, W. Tetrahedron Lett. 2004, 45, 7287. https://doi.org/10.1016/j.tetlet.2004.08.011
  13. Uno, H.; Yamashita, Y.; Kikuchi, M.; Watanabe, H.; Yamada, H.; Okujima, T.; Ogawa, T.; Ono, N. Tetrahedron Lett. 2005, 46, 1981. https://doi.org/10.1016/j.tetlet.2005.01.157
  14. Weidkamp, K. P.; Afzali, A.; Tromp, R. M.; Hamers, R. J. J. Am. Chem. Soc. 2004, 126, 12740. https://doi.org/10.1021/ja045228r
  15. Cheng, Y.-J.; Yang, S.-H.; Hsu, C.-S. Chem. Rev. 2009, 109, 5868. https://doi.org/10.1021/cr900182s
  16. Zheng, Q.; Jung, B. J.; Sun, J.; Katz, H. E. J. Am. Chem. Soc. 2010, 132, 5394. https://doi.org/10.1021/ja909111p
  17. Li, C.; Liu, M.; Pschirer, N. G.; Baumgarten, M.; Müllen, K. Chem. Rev. 2010, 110, 6817. https://doi.org/10.1021/cr100052z
  18. Kim, I.; Kim, T.-H.; Kang, Y.; Lim, Y.-B. Tetrahedron Lett. 2006, 47, 8689. https://doi.org/10.1016/j.tetlet.2006.10.020
  19. Kim, I.; Yoo, M.; Kim, T.-H. Tetrahedron 2007, 63, 9476. https://doi.org/10.1016/j.tet.2007.06.095
  20. Lee, M. G.; Hahn, S.-J.; Poduval, M. K. K.; Kim, T.-H. Bull. Korean Chem. Soc. 2011, 32, 2776. https://doi.org/10.5012/bkcs.2011.32.8.2776
  21. Pron, A.; Gawrys, P.; Zagorska, M.; Djurado, D.; Demadrille, R. Chem. Soc. Rev. 2010, 39, 2577. https://doi.org/10.1039/b907999h
  22. Zhu, Y.; Kulkarni, A. P.; Wu, P.-T.; Jenekhe, S. A. Chem. Mater. 2008, 20, 4200. https://doi.org/10.1021/cm702212w
  23. Bredas, J.-L.; Norton, J. E.; Cornil, J.; Coropceanu, V. Acc. Chem. Res. 2009, 42, 1691. https://doi.org/10.1021/ar900099h
  24. Zaumseil, J.; Donley, C. L.; Kim, J. S.; Friend, R. H.; Sirringhaus, H. Adv. Mater. 2006, 18, 2708. https://doi.org/10.1002/adma.200601080

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