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Solvent-free Synthesis, X-ray Structure Analysis and Electrochemical Properties of Ferrocenylchalcone containing Naphtalenyl Group

나프탈렌과 결합된 페로세닐 칼콘의 탈용매 고상합성, X-선 구조분석 및 전기화학 특성

  • Published : 2007.12.20

Abstract

Keywords

Ferrocenylchalcone;Solvent-free Reaction;X-ray Structure Analysis;Naphthalene;Electrochemistry

References

  1. Hayashi, T.; Togni, A. (eds.), Ferrocenes, VCH, Weinheim, 1995
  2. Schlogl, K.; Egger, H. Monatsh Chem. 1963, 94, 376 https://doi.org/10.1007/BF00900266
  3. Wu, X.; Wilairat, P.; Go, M. -L. Bioorg. Med. Chem. Lett. 2002, 12, 2299
  4. Belavaux-Nicot, B.; Fery-Forgues, S. Eur. J. Inorg. Chem. 1999, 1821
  5. Tarraga, A.; Molina, P.; Curiel, D.; Lopez, J. L.; Velasco, M. D. Tetrahedron 1999, 55, 14701 https://doi.org/10.1016/S0040-4020(99)00916-3
  6. Tarraga, A.; Molina, P.; Lopez, J. L. Tetrahedron Lett. 2000, 41, 2479 https://doi.org/10.1016/S0040-4039(00)00184-2
  7. Liu, W.; Xu, Q.; Chen, B.; Ma, Y. Synth. Commun. 2002, 32, 171 https://doi.org/10.1081/SCC-120001998
  8. Liu. W.; Xu, Q.; Chen, B.; Liang, Y.; Ma, Y.; Liu, W. J. Organometal. Chem. 2001, 637, 782 https://doi.org/10.1016/S0022-328X(01)00927-5
  9. Ji, S. J.; Shen, Z. L.; Wang, S. Y. Chin. Chem. Lett. 2003, 14, 663
  10. Villemin, D.; Martin, B.; Puciova, M.; Toma, S. J. Organometal. Chem. 1994, 484, 27 https://doi.org/10.1016/0022-328X(94)87181-7
  11. Sheldrick, G. M. SHELXTL, ver.5 Bruker AXS: Madison, Wisconsin, 1995
  12. Farrugia, L. J. J. Appl. Crystallogr. 1999, 32, 837 https://doi.org/10.1107/S0021889899006020
  13. Atkins, P.; Overton, T.; Rourke, J.; Weller, M.; Armstrong, F. Inorganic Chemistry, 4th ed., Oxford, UK, 2006

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