Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Oblique Columnar Assemblies of Polycatenar Molecules via Click Chemistry

  • Choi, Jin-Woo (Department of Chemistry and Institute of Nanosensor and Biotechnology, Dankook University) ;
  • Han, Ji-Hye (Department of Chemistry and Institute of Nanosensor and Biotechnology, Dankook University) ;
  • Ryu, Mee-Hi (Department of Chemistry and Institute of Nanosensor and Biotechnology, Dankook University) ;
  • Cho, Byoung-Ki (Department of Chemistry and Institute of Nanosensor and Biotechnology, Dankook University)
  • Received : 2010.09.16
  • Accepted : 2010.12.06
  • Published : 2011.03.20
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References

  1. Nguyen, H.-T.; Destrade, C.; Malthete, J. Adv. Mater. 1997, 9, 375.
  2. Gharbia, M.; Gharbi, A.; Nguyen, H. T.; Malthete, J. Curr. Opin. Colloid Interface Sci. 2002, 7, 312. https://doi.org/10.1016/S1359-0294(02)00087-0
  3. Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem., Int. Ed. 2002, 41, 2596. https://doi.org/10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
  4. Fournier,D.; Hoogenboom, R.; Schubert,U. S.Chem. Soc. Rev. 2007, 36, 1369. https://doi.org/10.1039/b700809k
  5. Hua, C.; Peng, S.-M.; Dong, C.-M. Macromolecules 2008, 41, 6686. https://doi.org/10.1021/ma800857d
  6. Lin,W.; Fu, Q.; Zhang, Y.; Huang, J. Macromolecules 2008, 41, 4127. https://doi.org/10.1021/ma702404t
  7. Franc, G.; Kakkar, A. Chem. Commun. 2008, 5267.
  8. Lee, J. W.; Kim, B.-K. Bull. Korean Chem. Soc. 2005, 26, 658. https://doi.org/10.5012/bkcs.2005.26.4.658
  9. Gallardo, H.; Ely, F.; Bortoluzzi, A. J.; Conte, G. Liq. Cryst. 2005, 32, 667. https://doi.org/10.1080/02678290500139732
  10. Cui, Z.; Zhang, Y.; He, S. Colloid Polym. Sci. 2008, 286, 1553. https://doi.org/10.1007/s00396-008-1916-9
  11. Xia, Y.; Verduzco, R.; Grubbs, R. H.; Kornfield, J. A. J. Am. Chem. Soc. 2008, 130, 1735. https://doi.org/10.1021/ja077192j
  12. Saravanan, C.; Senthil, S.; Kannan, P. J. Polym. Sci., Part A: Polym. Chem. 2008, 46, 7843. https://doi.org/10.1002/pola.23090
  13. Srividhya,D.;Manjunathan, S.; Thirumaran, S.; Saravanan, C; Senthil, S. J. Mol. Struct. 2009, 927, 7. https://doi.org/10.1016/j.molstruc.2009.01.035
  14. Ryu, M.-H.; Choi, J.-W.; Cho, B.-K. J. Mater. Chem. 2010, 20, 1806. https://doi.org/10.1039/b921685e
  15. Choi, J.-W.; Ryu,M.-H.; Lee, E.; Cho, B.-K. Chem. Eur. J. 2010, 16, 9006. https://doi.org/10.1002/chem.201001337
  16. Beltran, E.; Serrano, J. L.; Sierra, T.; Gimenez, R. Org. Lett. 2010, 12, 1404. https://doi.org/10.1021/ol902900y
  17. Mespouille, L.; Vachaudez, M.; Suriano, F.; Gerbaux, P.; Coulembier, O.; Degee, P.; Flammang, R.; Dubois, P. Macromol. Rapid Commun. 2007, 28, 2151. https://doi.org/10.1002/marc.200700400
  18. Han, T. H.; Kim, J.; Park, J. S.; Park, C. B.; Ihee, H.; Kim, S. O. Adv. Mater. 2007, 19, 3924. https://doi.org/10.1002/adma.2007001839
  19. Park, J. S.;Han, T.H.;Oh, J.K.; Kim, S. O. Macromol. Chem. Phys. 2009, 210, 1283. https://doi.org/10.1002/macp.200900202
  20. Serrano, J. L.; Sierra, T. Coord. Chem. Rev. 2003, 242, 73. https://doi.org/10.1016/S0010-8545(03)00061-4
  21. Rais, K.; Daoud, M.; Gharbia, M.; Gharbi, A.; Nguyen, H. T. ChemPhysChem. 2001, 2, 45. https://doi.org/10.1002/1439-7641(20010119)2:1<45::AID-CPHC45>3.0.CO;2-U
  22. Percec, V.; Ahn, C.-H.; Bera, T. K.; Ungar, G.; Yeardley, D. J. P. Chem. Eur. J. 1999, 5, 1070. https://doi.org/10.1002/(SICI)1521-3765(19990301)5:3<1070::AID-CHEM1070>3.0.CO;2-9
  23. Donnio, B.; Heinrich, B.; Allouchi, H.; Kain, J.; Diele, S.; Guillon, D.; Bruce,D.W. J. Am. Chem. Soc. 2004, 126, 15258. https://doi.org/10.1021/ja0471673
  24. Yasuda, T.; Kishimoto, K.; Kato, T. Chem. Commun. 2006, 3399.
  25. Wurthner, F.; Thalacker, C.; Diele, S.; Tschierske, C. Chem. Eur. J. 2001, 7, 2245. https://doi.org/10.1002/1521-3765(20010518)7:10<2245::AID-CHEM2245>3.0.CO;2-W
  26. Ribeiro, A. C.; Heinrich, B.; Cruz, C.; Nguyen, H. T.; Diele, S.; Schröder,M. W.; Guillon, D. Eur. Phys. J. E 2003, 10, 143. https://doi.org/10.1140/epje/e2003-00018-9
  27. Yasuda, T.; Ooi,H.;Morita, J.; Akama,Y.;Minoura,K.; Funahashi, M.; Shimomura, T.; Kato, T. Adv. Funct.Mater. 2009, 19, 411. https://doi.org/10.1002/adfm.200801268
  28. Seo, J.; Kim, S.; Gihm, S. H.; Park, C. R.; Park, S. Y. J. Mater. Chem. 2007, 17, 5052. https://doi.org/10.1039/b711883j

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