Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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The New Fluorescent Naphthalic Imide Derivatives Having the Inductive Ending Group

  • Received : 2009.11.06
  • Accepted : 2010.02.24
  • Published : 2010.05.20
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Abstract

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References

  1. Minta, A.; Kao, J. P. Y.; Tsien, R. Y. J. Biol. Chem. 1989, 264, 8171.
  2. Balzani, V.; Juris, A.; Venturi, M.; Campagna, S.; Serroni, S. Chem. Rev. 1996, 96, 759. https://doi.org/10.1021/cr941154y
  3. Soper, S. A.; Warner, I. M.; McGown, L. B. Anal. Chem. 1998, 70, 477R. https://doi.org/10.1021/a1980019y
  4. Campagna, S.; Serroni, S.; Bodige, S.; MacDonnell, F. M. Inorg. Chem. 1999, 38, 692. https://doi.org/10.1021/ic9811852
  5. Gestwicki, J. E.; Kiessling, L. L. Nature 2002, 415, 81. https://doi.org/10.1038/415081a
  6. Meyer, T. J. Pure Appl. Chem. 1986, 58, 1193. https://doi.org/10.1351/pac198658091193
  7. Boyde, S.; Strouse, G. F.; Jones, W. E., Jr.; Meyer, T. J. J. Am. Chem. Soc. 1989, 111, 7448. https://doi.org/10.1021/ja00201a027
  8. Winkler, J. R.; Gray, H. B. Chem. Rev. 1992, 92, 369. https://doi.org/10.1021/cr00011a001
  9. Vogtle, F.; Frank, M.; Nieger, M.; Belser, P.; Zelewsky, A. V.; Balzani, V.; Barigelletti, F.; Cola, L. D.; Flamigni, L. Angew. Chem., Int. Ed. Engl. 1993, 32, 1643. https://doi.org/10.1002/anie.199316431
  10. Choi, C.-S.; Kim, M.-K.; Jeon, K.-S; Lee, K.-H. J. Lumi. 2004, 109, 121. https://doi.org/10.1016/j.jlumin.2004.01.091
  11. Choi, C.-S.; Jeon, K.-S; Lee, K.-H. J. Photosci. 2004, 11(2), 71.
  12. Choi, C.-S.; Mutai, T.; Arita, S.; Araki, K. J. Chem. Soc., Perkin Trans. 2 2000, 243.
  13. Choi, C.-S.; Mishra, L.; Mutai, T.; Araki, K. Bull. Chem. Soc. Jpn. 2000, 73, 2051. https://doi.org/10.1246/bcsj.73.2051
  14. Choi, C.-S.; Jeon, K.-S.; Jeon, K.-H.; Yoon, M.; Kwak, M.; Lee, S. W.; Kim, I. T. Bull. Korean Chem. Soc. 2006, 27(10), 1601. https://doi.org/10.5012/bkcs.2006.27.10.1601
  15. Lee, K.-H.; Choi, C.-S.; Jeon, K.-S. J. Photosci. 2002, 9(3), 71.
  16. Demas, J. N.; Crosby, G. A. J. Phys. Chem. 1971, 75, 991. https://doi.org/10.1021/j100678a001

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