Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Preparation of the New Macropolycycle Containing N-CH2-N Linkages and Its Reaction with Methanol in the Presence of Cu2+ Ion: Formation of a Copper(II) Complex Bearing Two N-Methoxymethyl Groups

  • Published : 2007.03.20
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References

  1. Costamagna, J.; Ferraudi, G.; Matsuhiro, B.; Vampus-Vallette, M.; Canales, J.; Villagran, M.; Vargas, J.; Aguirre, M. J. Coord. Chem. Rev. 2000, 196, 125
  2. Wainwright, K. P. Coord. Chem. Rev. 1997, 166, 35 https://doi.org/10.1016/S0010-8545(97)00003-9
  3. Siegfried, L.; Comparone, A.; Neuburger, M.; Kaden, T. A. Dalton Trans. 2005, 30
  4. Lukes, I.; Kotek, J.; Vojtisek, P.; Hermann, P. Coord. Chem. Rev. 2001, 216-217, 287
  5. Kim, K. J.; Jung, D. S.; Kim, D. S.; Choi, C. K.; Park, K. M.; Byun, J. C. Bull. Korean Chem. Soc. 2006, 27, 1747 https://doi.org/10.5012/bkcs.2006.27.11.1747
  6. Mayer, M.; Dahaoui-Gindrey, V.; Lecomte, C.; Guilard, R. Coord. Chem. Rev. 1998, 178-180, 1313
  7. Kang, S.-G.; Kim, M.-S.; Choi, J.-S.; Whang, D.; Kim, K. J. Chem. Soc., Dalton Trans. 1995, 363
  8. Kang, S.-G.; Nam, K.; Kweon, J. K.; Jung, S.-K.; Lee, U. Bull. Korean Chem. Soc. 2006, 27, 577 https://doi.org/10.5012/bkcs.2006.27.4.577
  9. Kang, S.-G.; Ryu, K. Bull. Korean Chem. Soc. 2000, 21, 535
  10. Kang, S.-G.; Song, J.; Jeong, J. H. Inorg. Chim. Acta 2004, 357, 605 https://doi.org/10.1016/j.ica.2003.06.006
  11. Suh, M. P.; Kang, S.-G.; Goedken, V. L.; Park, S.-H. Inorg. Chem. 1991, 30, 365
  12. Hubin, T. J. Coord. Chem. Rev. 2003, 241, 27 https://doi.org/10.1016/S0010-8545(02)00307-7
  13. Alcock, N. W.; Moore, P.; Mok, K. F. J. Chem. Soc., Perkin Trans. II 1980, 1186
  14. Tripier, R.; Lagrange, J.-M.; Espinosa, E.; Denat, F.; Guilard, R. Chem. Commun. 2001, 2278
  15. Comparone, A.; Kaden, T. A. Helv. Chim. Acta 1998, 81, 1765 https://doi.org/10.1002/(SICI)1522-2675(19981007)81:10<1765::AID-HLCA1765>3.0.CO;2-N
  16. Bucher, C.; Royal, G.; Barbe, J.-M.; Guilard, R. Tetrahedron Lett. 1999, 40, 2315
  17. Batsanov, A. S.; Goeta, A. E.; Howard, J. A. K.; Maffeo, D.; Puschmann, H.; Williams, J. A. G. Polyhedron 2001, 20, 981 https://doi.org/10.1016/S0277-5387(01)00737-9
  18. Royal, G.; Dahaoui-Gindrey, V.; Dahaoui, S.; Tabard, A.; Guilard, R.; Pullumbi, P.; Lecomte, C. Eur. J. Org. Chem. 1998, 1971
  19. Alder, R. W.; Heilbronner, E.; Honegger, E.; McEwen, A. B.; Moss, R. E.; Olefirowicz, E.; Petillo, P. A.; Sessions, R. B.; Weisman, G. R.; White, J. M.; Yang, Z.-Z. J. Am. Chem. Soc. 1993, 115, 6580
  20. Suh, M. P.; Choi, J.; Kang, S.-G.; Shin, W. Inorg. Chem. 1989, 28, 1763
  21. Suh, M. P.; Lee, J.; Han, M. Y.; Yoon, T. S. Inorg. Chem. 1997, 36, 5651 https://doi.org/10.1021/ic970020a
  22. Frisch, M. J. et al. Gaussian 03, Revision B.05; Gaussian, Inc.: Pittsburgh, PA, 2003
  23. Saunders, M. J. Am. Chem. Soc. 1987, 109, 3150 https://doi.org/10.1021/ja00244a051
  24. Saunders, M. J. Comput. Chem. 1989, 10, 203 https://doi.org/10.1002/jcc.540100207
  25. Serena Software, Box 3076, Bloomington, IN 47402-3076, U. S. A
  26. Allinger, N. L.; Yuh, Y. H.; Lii, J.-H. J. Am. Chem. Soc. 1989, 111, 8551
  27. Becke, A. D. J. Chem. Phys. 1993, 98, 5648 https://doi.org/10.1063/1.464913
  28. Ditchfield, R. Mol. Phys. 1974, 27, 789 https://doi.org/10.1080/00268977400100711
  29. Wolinski, K.; Hinton, J. K.; Pulay, P. J. Am. Chem. Soc. 1990, 112, 8251 https://doi.org/10.1021/ja00179a005
  30. Kang, S.-G.; Kweon, J. K.; Jung, S.-K. Bull. Korean Chem. Soc. 1991, 12, 483
  31. STOE-STADI 4 (revision 1.09), X-RED (revision 1.09), & XSHAPE (revision 2.05). X-Ray Structure Evalutation Package; STOE-Cie Gmbh, Hilpertstrasse 10, D64295 Darmstadt, Germany, 1996
  32. Sheldrick, G. M. Acta Crystallogr. 1990, A46, 467
  33. Sheldrick, G. M. SHELXL97-2; University of Gottingen: Germany, 1997
  34. Farrugia, L. J. J. Appl. Crystallogr. 1997, 30, 565

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