DOI QR코드

DOI QR Code

Synthesis, Complexation and Fluorescence Properties of N-Anthracenylmethyl Dipodal Ligand with Quinoline End-Group

  • Kang, Young-Jin (Division of Science Education & Department of Chemistry, Kangwon National University) ;
  • Moon, Seok-Tae (Research Institute of Natural Science and Department of Chemistry (BK21), Gyeongsang National University) ;
  • Park, Sunhong (Research Institute of Natural Science and Department of Chemistry (BK21), Gyeongsang National University) ;
  • Kim, Jin-Ho (Division of Science Education & Department of Chemistry, Kangwon National University) ;
  • Lee, Shim Sung (Research Institute of Natural Science and Department of Chemistry (BK21), Gyeongsang National University) ;
  • Park, Ki-Min (Research Institute of Natural Science and Department of Chemistry (BK21), Gyeongsang National University)
  • Published : 2007.05.20

Abstract

Keywords

References

  1. Valeur, B. Molecular Fluorescence Principles and Applications, Wiley-VCH: Weinheim, 2001
  2. Fluorescent Chemosensors for Ion and Molecular Recognition; Czamik, A. W., Ed.; American Chemical Society: Washington, D.C., 1993
  3. Chemosensors for Ion and Molecular Recognition; Desvergne, J. P.; Czarmik, A. W. Eds.; Kluwer: Dordrecht, The Netherlands, 1997
  4. Wang, S.; Seward, C. Encyclopedia of Supramolecular Chemistry; Atwood, J. L.; Steed, J. W. Eds.; Dekker: New York, 2004; p 816
  5. Czarnik, A. W. Acc. Chem. Res. 1994, 27, 302 https://doi.org/10.1021/ar00046a003
  6. Inoue, M. B.; Medrano, F.; Inoue, M.; Raitsimring, A.; Fernando, Q. Inorg. Chem. 1997, 36, 2335 https://doi.org/10.1021/ic9614374
  7. Kim, S. K.; Lee, S. H.; Lee, J. Y.; Bartsch, R. A.; Kim, J. S. J. Am. Chem. Soc. 2004, 126, 16499 https://doi.org/10.1021/ja045689c
  8. Grandini, P.; Mancin, F.; Tecilla, P.; Scrimin, P.; Tonellato, U. Angew Chem. Int. Ed. Engl. 1999, 38, 3061 https://doi.org/10.1002/(SICI)1521-3773(19991018)38:20<3061::AID-ANIE3061>3.0.CO;2-A
  9. Schliche, B.; Belser, P.; De Cola, L.; Sabbioni, E.; Balzani, V. J. Am. Chem. Soc. 1999, 121, 4207 https://doi.org/10.1021/ja990044b
  10. Rurack, K.; Kollmannsberger, M.; Resch-Genger, U.; Daub, J. J. Am. Chem. Soc. 1999, 121, 5073
  11. Vogtle, F.; Weber, E. Angew. Chem. Int. Ed. Engl. 1979, 18, 753
  12. Lee, Y. O.; Lee, J. Y.; Quang, D. T.; Lee, M. H.; Kim, J. S. Bull. Korean Chem. Soc. 2006, 27, 1469 https://doi.org/10.5012/bkcs.2006.27.9.1469
  13. Lee, S. S.; Jung, J. H.; Cho, S. B.; Kim, J. S.; Kim, J.; Kim, S.-J. Bull. Korean Chem. Soc. 1992, 13, 704
  14. Lee, S. S.; Yoon, I.; Park, K.-M.; Jung, J. H.; Lindoy, L. F.; Nezhadali, A.; Rounaghi, G. Dalton Trans. 2002, 2180
  15. In, S.; Kang, J. Bull. Korean Chem. Soc. 2005, 26, 1121 https://doi.org/10.5012/bkcs.2005.26.7.1121
  16. Yoon, I.; Lee, Y. H.; Jung, J. H.; Park, K.-M.; Kim, J.; Lee, S. S. Inorg. Chem. Commun. 2002, 5, 820
  17. Park, K.-M.; Moon, S.-T.; Kang, Y. J.; Kim, H. J.; Seo, J.; Lee, S. S. Inorg. Chem. Commun. 2006, 9, 671 https://doi.org/10.1016/j.inoche.2006.03.028
  18. Tummler, B.; Maass, G.; Vogtle, F.; Sieger, H.; Heimann, U.; Weber, E. J. Am. Chem. Soc. 1979, 101, 2588 https://doi.org/10.1021/ja00504a014
  19. Bordunov, A. V.; Hellier, P. C.; Bradshaw, J. S. J. Org. Chem. 1995, 60, 6097 https://doi.org/10.1021/jo00124a022
  20. Varnes, A. W.; Dodson, R. B.; Wehry, E. L. J. Am. Chem. Soc. 1972, 94, 946 https://doi.org/10.1021/ja00758a037
  21. Cloninger, M. J.; Whitlock, H. W. J. Org. Chem. 1998, 63, 6153 https://doi.org/10.1021/jo980193x
  22. Demas, J. N.; Crosby, G. A. J. Phys. Chem. 1971, 75, 991 https://doi.org/10.1021/j100678a001
  23. Bruker, SAINTPLUS NT Version 6.22. Software Reference Manual; Bruker AXS: Madison, Wisconsin, 2000
  24. Bruker, SHELXTL NT Version 6.10. Program for Solution and Refinement of Crystal Structures; Bruker AXS: Madison, Wisconsin, 2000

Cited by

  1. Synthesis, Structural Characterization, and Physical Properties of Alkylammonium Derivative Complex with Acyclic Crown Ether Analog vol.32, pp.6, 2011, https://doi.org/10.5012/bkcs.2011.32.6.2097
  2. ions vol.25, pp.3, 2013, https://doi.org/10.1080/10610278.2012.733818
  3. Selectivity vol.34, pp.5, 2013, https://doi.org/10.5012/bkcs.2013.34.5.1429
  4. Improvement of Luminescence Quantum Efficiency by Intermolecular Interaction vol.28, pp.10, 2007, https://doi.org/10.5012/bkcs.2007.28.10.1807
  5. Surprisingly stable ammonium ion complex of a non-cyclic crown-type polyether: solid and solution studies vol.34, pp.4, 2007, https://doi.org/10.1039/c0nj00074d
  6. A Highly Hg(II)-selective Chemosensor with Unique Diarylethene Fluorophore vol.31, pp.5, 2007, https://doi.org/10.5012/bkcs.2010.31.5.1371
  7. Synthesis of New Aza‐ and Thia‐Crown Ether Based Amino Acids vol.5, pp.9, 2007, https://doi.org/10.1002/slct.202000122