Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Discrimination of Primary Alkylamines Using Azobenzene-appended Calix[4]arene Derivatives in Solution and in the Solid State

  • Cho, Eun-Jin (Department of Materials Science and Engineering, KAIST) ;
  • Jeong, Il-Yun (Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute) ;
  • Lee, Soo-Jin (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Seo, Ju-Beom (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Kim, Hyun-Jung (Department of Chemistry, Korea University) ;
  • Kim, Eun-Jeong (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Lee, Shim-Sung (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Kang, Jeong-Ku (Department of Materials Science and Engineering, KAIST) ;
  • Kim, Jong-Seung (Department of Chemistry, Korea University) ;
  • Jung, Jong-Hwa (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University)
  • Published : 2007.12.20
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References

  1. Andreetti, G. D.; Ugozzoli, F.; Ungaro, R.; Pochini, A. In Inclusion Compounds; Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Eds.; Oxford University Press: New York, 1991; Vol. 4
  2. Cho, E. J.; Yeo, H. M.; Ryu, B. J.; Jeong, H. A.; Nam, K. C. Bull. Korean Chem. Soc. 2006, 27, 1967 https://doi.org/10.5012/bkcs.2006.27.12.1967
  3. Hinsberg, O. Ber. 1890, 23, 2962 https://doi.org/10.1002/cber.189002302215
  4. Solomons, G.; Fryhle, C. Organic Chemistry, 7th ed.; John Wiley & Sons Inc.: New York, 2002; p 975
  5. Cram, D. J.; Cram, J. M. Acc. Chem. Res. 1978, 11, 8 https://doi.org/10.1021/ar50121a002
  6. Stoddart, J. F. Chem. Soc. Rev. 1979, 8, 85 https://doi.org/10.1039/cs9790800085
  7. Mock, W. L.; Shih, N.-Y. J. Org. Chem. 1986, 51, 4440
  8. Hayward, R. C. Chem. Soc. Rev. 1983, 12, 285 https://doi.org/10.1039/cs9831200285
  9. Palomares, E.; Vilar, R.; Green, A.; Durrant, J. R. Adv. Funct. Mater. 2004, 14, 111 https://doi.org/10.1002/adfm.200304444
  10. Shi, J.; Zhu, Y.; Zhang, X.; Baeyens, W. R. G.; Garcia-Campana, A. M. Trends Anal. Chem. 2004, 23, 351 https://doi.org/10.1016/S0165-9936(04)00519-9
  11. Obare, S. O.; Hollowell, R. E.; Murphy, C. J. Langmuir 2002, 18, 10407 https://doi.org/10.1021/la0260335
  12. Wirnsberger, G.; Scott, B. J.; Stucky, G. D. Chem. Commun. 2001, 119
  13. Mercier, L.; Pinnavaia, T. J. Adv. Mater. 1997, 9, 500 https://doi.org/10.1002/adma.19970090611
  14. Metivier, R.; Leray, I.; Lebeau, B.; Valeur, B. J. Mater. Chem. 2005, 15, 2965 https://doi.org/10.1039/b501897h
  15. Balaji, T.; Sasidharan, M.; Matsunaga, H. Anal. Bioanal. Chem. 2006, 384, 488 https://doi.org/10.1007/s00216-005-0187-2
  16. Desacalzo, A. B.; Jimenez, D.; Marcos, M. D.; Manez, R. M.; Soto, J.; El Haskouri, J.; Guillem, C.; Beltran, D.; Amoros, P.; Borrachero, M. V. Adv. Mater. 2002, 14, 966 https://doi.org/10.1002/1521-4095(20020704)14:13/14<966::AID-ADMA966>3.0.CO;2-G
  17. Boiocchi, M.; Bonizzoni, M.; Fabbrizzi, L.; Piovani, G.; Taglietti, A. Angew. Chem. 2004, 116, 3935 https://doi.org/10.1002/ange.200460036
  18. Boiocchi, M.; Bonizzoni, M.; Fabbrizzi, L.; Piovani, G.; Taglietti, A. Angew. Chem. Int. Ed. 2004, 43, 3847 https://doi.org/10.1002/anie.200460036
  19. Comes, M.; Lopez, G. R.; Marcos, M. D.; Manez, R. M.; Sancenon, F.; Soto, J.; Villaescusa, L. A.; Amoros, P.; Beltran, D. Angew. Chem. 2005, 117, 2978; Angew. Chem. Int. Ed. 2005, 44, 2918 https://doi.org/10.1002/ange.200461511
  20. Han, S.; Sujandi; Park, S. Bull. Korean Chem. Soc. 2005, 26, 1381 https://doi.org/10.5012/bkcs.2005.26.9.1381
  21. Kim, J. S.; Shon, O. J.; Lee, J. K.; Lee, S. H.; Kim, J. Y.; Park, K. M.; Lee, S. S. J. Org. Chem. 2002, 67, 1372 https://doi.org/10.1021/jo0108921
  22. Kim, J. Y.; Kim, G. C.; Kim, C. R.; Lee, S. H.; Lee, J. H.; Kim, J. S. J. Org. Chem. 2003, 68, 1933 https://doi.org/10.1021/jo020684o
  23. Halouani, H.; Dumazet-Bonnamour, I.; Lamartine, R. Tetrahedron Lett. 2002, 43, 3785
  24. Halouani, H.; Dumazet-Bonnamour, I.; Duchamp, C.; Bavoux, C.; Ehlinger, N.; Perrin, M.; Lamartine, R. Eur. J. Org. Chem. 2002, 24, 4202
  25. Connors, K. A. Binding Constants; Wiley: New York, 1987
  26. Cobben, P. L. H. M.; Egberink, R. J. M.; Bohmer, J. R. P.; Verboom, W.; Reinhoudt, D. N. J. Am. Chem. Soc. 1992, 114, 10573 https://doi.org/10.1021/ja00052a063
  27. Kim, J. S.; Jung, J. H.; Lee, S. J.; Hwang, I.; Singh, N. J.; Kim, S. K.; Lee, S. H.; Kim, H. J.; Keum, C. S.; Lee, J. W.; Kim, K. S. Chem. Eur. J. 2007, 13, 3082 https://doi.org/10.1002/chem.200600905

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