Bulletin of the Korean Chemical Society

  • 제31권5호
  • /
  • Pages.1387-1388
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  • 2010
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Cathodoluminescence Properties of In2O3-coated Y2O3:Eu3+ Phosphors

  • Eun, So-Hee (School of Biotechnology, Yeungnam University) ;
  • Choi, In-Ho (School of Biotechnology, Yeungnam University) ;
  • Shim, Sang-Hee (School of Biotechnology, Yeungnam University)
  • 투고 : 2010.02.17
  • 심사 : 2010.03.09
  • 발행 : 2010.05.20
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참고문헌

  1. Lobo, R.; Prabhu, K. S.; Shirwaikar, A. J. Pharm. Pharmacol. 2009, 61, 13. https://doi.org/10.1211/jpp/61.01.0003
  2. Matsuda, H.; Morikawa, T.; Ninomiya, K.; Yoshikawa, M. Bioorg. Med. Chem. 2001, 9, 909. https://doi.org/10.1016/S0968-0896(00)00306-0
  3. Wilson, B.; Abraham, G.; Manju, V. S.; Mathew, M.; Vimala, B.; Sundaresan, S.; Nambisan, B. J. Ethnopharmacol. 2005, 99, 147. https://doi.org/10.1016/j.jep.2005.02.004
  4. Raghuveer, G.; Ali, M.; Eranna, D.; Ramachandra, S. Indian J. Traditional Knowledge 2004, 2, 375.
  5. Navarro, D. F.; Souza, M.; Neto, R. A.; Golin, V.; Niero, R.; Yunes, R. A.; Monache, F. D.; Filho, V. C. Phytomedicine 2002, 9, 427. https://doi.org/10.1078/09447110260571670
  6. Matsuda, H.; Tewtrakul, S.; Morikawa, T.; Nakamura, A.; Yoshikawa, M. Bioorg. Med. Chem. 2004, 12, 5891. https://doi.org/10.1016/j.bmc.2004.08.027
  7. Matsuda, H.; Ninomiya, K.; Morikawa, T.; Yoshikawa, M. Bioorg. Med. Chem. Lett. 1998, 8, 339. https://doi.org/10.1016/S0960-894X(98)00021-3
  8. Makabe, H.; Maru, N.; Kuwabara, A.; Kamo, T.; Hirota, M. Nat. Prod. Res. 2006, 20, 680. https://doi.org/10.1080/14786410500462900
  9. Seo, W.-G.; Hwang, J.-C.; Kang, S.-K.; Jin, U.-H.; Suh, S.-J.; Moon, S.-K.; Kim, C.-H. J. Ethnopharmacol. 2005, 101, 249. https://doi.org/10.1016/j.jep.2005.04.037
  10. Kuroyanagi, M.; Natori, S. Yakugaku Zasshi 1970, 90, 1467. https://doi.org/10.1248/yakushi1947.90.11_1467
  11. Hikino, H.; Takahashi, S.; Sakurai, Y.; Takemoto, T. Chem. Pharm. Bull. 1968, 16, 1081. https://doi.org/10.1248/cpb.16.1081
  12. Hikino, H.; Tori, K.; Horibe, I.; Kuriyama, K. J. Chem. Soc. (c) 1971, 4, 688.
  13. Shiobara, Y.; Asakawa, Y.; Kodama, M.; Takemoto, T. Phytochemistry 1986, 25, 1351. https://doi.org/10.1016/S0031-9422(00)81288-1
  14. Li, M.; Zhou, X.; Zhao, Y.; Wang, D. P.; Hu, X. N. Bull. Korean Chem. Soc. 2009, 30, 2287. https://doi.org/10.5012/bkcs.2009.30.10.2287
  15. Crabbe, P. Chem. Ind. 1969, 917.
  16. Albach, R. F.; Redman, G. H. Phytochemistry 1969, 8, 127. https://doi.org/10.1016/S0031-9422(00)85805-7

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