Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Characterization of Melanin-TiO2 Complexes Using FT-IR and 13C Solid-state NMR Spectroscopy

  • Park, Tae-Joon (Department of Chemistry, Hankuk University of Foreign Studies) ;
  • Kim, Jin-Soo (New Chemistry Research Division, Korea Research Institute of Chemical Technology) ;
  • Kim, Tae-Kyung (New Chemistry Research Division, Korea Research Institute of Chemical Technology) ;
  • Park, Hee-Moon (New Chemistry Research Division, Korea Research Institute of Chemical Technology) ;
  • Choi, Sung-Sup (Department of Chemistry, Hankuk University of Foreign Studies) ;
  • Kim, Yongae (Department of Chemistry, Hankuk University of Foreign Studies)
  • Published : 2008.12.20
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References

  1. Chedekel, M. R.; Fitzpatrick, T. B.; Zeise, L. Melanin: Its Role in Human Photoprotection; Valdenmar Publishing Company: 1995; pp 11-12.
  2. Kolias, N. S. R.; Zeise, L.; Chedekel, M. R. J. Photochem. Photobiol. B: Biol. 1991, 9, 135. https://doi.org/10.1016/1011-1344(91)80147-A
  3. Moire, C.; Deflandre, A.; Junino, A.; Goetz, N. Abstr. 3rd Annual Meeting of the European Society for Pigment Cell Research; Amsterdam, 1991; p 39.
  4. Scalia, M.; Geremia, E.; Corsaro, C.; Sautoro, C.; Baretta, D.; Sichel, G. Pigm. Cell Res. 1990, 3, 115. https://doi.org/10.1111/j.1600-0749.1990.tb00330.x
  5. Pathak, M. S.; Jimbow, K.; Szabo, G.; Fitzpatric, T. B. Photochem. Photobiol. Rev. 1976, 2, 211.
  6. Prota, G. Melanins and Melanogenesis; Academic Press: Sandiego, 1992; pp 152-290.
  7. Crippa, R.; Horak, V.; Prota, G.; Svoronos, P.; Wolfram, L.; Brossi, A. Alkaloids; Academic Press: New York, 1989; pp 253-323.
  8. Riley, P. A. Int. J. Biochem. Cell Biol. 1997, 29, 1235. https://doi.org/10.1016/S1357-2725(97)00013-7
  9. Aime, S.; Fasano, M.; Bergamasco, B.; Lopiano, L.; Quattrocolo, G. Adv. Neurol. 1996, 69, 263.
  10. Blesa, M. A.; Weisz, A. D.; Morando, P. J.; Salfity, J. A.; Magaz, G. E.; Regazzoni, A. E. Coord. Chem. Rev. 2000, 196, 31. https://doi.org/10.1016/S0010-8545(99)00005-3
  11. Rodriguez, R.; Blesa, M. A.; Regazzoni, A. E. J. Coll. and Inter. Sci. 1996, 177, 122. https://doi.org/10.1006/jcis.1996.0012
  12. Borgias, B. A.; Cooper, S. R.; Koh, Y. B.; Raymond, K. N. Inorg. Chem. 1984, 23, 1009. https://doi.org/10.1021/ic00176a005
  13. Connor, P. A.; Dobson, K. D.; McQuillan, A. J. Langmuir 1995, 11, 4193. https://doi.org/10.1021/la00011a003
  14. Moser, J.; Punchihewa, S.; Infelta, P. P.; Grätzel, M. Langmuir 1991, 7, 3012. https://doi.org/10.1021/la00060a018
  15. Martin, S. T.; Kesselman, J. M.; Park, D. S.; Lewis, N. S.; Hoffman, M. R. Environ. Sci. Technol. 1996, 30, 2535. https://doi.org/10.1021/es950872e
  16. Stainsack, J.; Mangrich, A. S.; Maia, C. M. B. F.; Machado, V. G.; Santos, J. C. P.; Nakagaki, S. Inorg. Chim. Acta 2003, 356, 243. https://doi.org/10.1016/S0020-1693(03)00474-2
  17. Christ, R. W. Cos. & Toil. Mag. 2003, 118, 73.
  18. Monte, S. J.; Island, S.; Bruins, P. F. U. S. Patent, 4, 098, 758, 1978.
  19. Schlossman, D. S.; Orange, W. U. S. Patent, 5, 356, 617, 1994.
  20. Kim, J. W.; Shim, J. W.; Bae, J. H.; Han, S. H.; Kim, H. K.; Chang, I. S.; Kang, H. H.; Suh, K. D. Colloid Polym. Sci. 2002, 280, 584. https://doi.org/10.1007/s00396-002-0655-6
  21. Jang, D. I. Korea Patent, 0084598, 2004.
  22. Aime, S.; Crippa, P. R. Pigm. Cell Res. 1988, 1, 355. https://doi.org/10.1111/j.1600-0749.1988.tb00132.x
  23. Hartmann, S. R.; Hahn, E. L. Phys. Rev. 1962, 128, 2043.
  24. Giuseppe, P. Pigm. Cell Res. 2000, 13, 283. https://doi.org/10.1034/j.1600-0749.2000.130412.x
  25. Ghiani, S.; Baroni, S.; Burgio, D.; Digilio, G.; Fukuhara, M.; Martino, P.; Monda, K.; Nervi, C.; Kiyomine, A.; Aime, S. Magn. Reson. Chem. 2008, 46, 471. https://doi.org/10.1002/mrc.2202
  26. Kim, Y.; Kim, A. Bull. Kor. Chem. Soc. 2002, 23, 1729. https://doi.org/10.5012/bkcs.2002.23.12.1729
  27. Kim, Y. Bull. Kor. Chem. Soc. 2003, 24, 1281. https://doi.org/10.5012/bkcs.2003.24.9.1281
  28. Kim, Y. Bull. Kor. Chem. Soc. 2006, 27, 386. https://doi.org/10.5012/bkcs.2006.27.3.386

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