DOI QR코드

DOI QR Code

Template Syntheses, Crystal Structures and Supramolecular Assembly of Hexaaza Macrocyclic Copper(II) Complexes

  • Kim, Taehyung (Department of Chemistry, Pukyong National University) ;
  • Lough, Alan J. (Department of Chemistry, University of Toronto) ;
  • Kim, Ju Chang (Department of Chemistry, Pukyong National University)
  • Received : 2013.03.12
  • Accepted : 2013.03.27
  • Published : 2013.06.20

Abstract

Keywords

References

  1. Chakrabarty, R.; Mukherjee, P. S.; Stang, P. J. Chem. Rev. 2011, 111, 6810. https://doi.org/10.1021/cr200077m
  2. Bassanetti, I.; Mezzadri, F.; Comotti, A.; Sozzani, P.; Gennari, M.; Calestani, G.; Marchio, L. J. Am. Chem. Soc. 2012, 134, 9142. https://doi.org/10.1021/ja303940d
  3. Brown, C. J.; Miller, G. M.; Johnson, M. W.; Bergman, R. G.; Raymond, K. N. J. Am. Chem. Soc. 2011, 133, 11964. https://doi.org/10.1021/ja205257x
  4. Wu, C.-D.; Hu, A.; Zhang, L.; Lin, W. J. Am. Chem. Soc. 2005, 127, 8940. https://doi.org/10.1021/ja052431t
  5. Pramanik, A.; Abbina, S.; Das, G. Polyhedron 2007, 26, 5225. https://doi.org/10.1016/j.poly.2007.07.033
  6. Yamada, Y. M. A.; Sarkar, S. M.; Uozumi, Y. J. Am. Chem. Soc. 2012, 134, 3190. https://doi.org/10.1021/ja210772v
  7. Schwarz, G.; Bodenthin, Y.; Tomkowicz, Z.; Haase, W.; Geue, T.; Kohlbrecher, J.; Pietsch, U.; Kurth, D. G. J. Am. Chem. Soc. 2011, 133, 547. https://doi.org/10.1021/ja108416a
  8. Hazra, S.; Mondal, S.; Fleck, M.; Sasmal, S.; Sanudo, E. C.; Mohanta, S. Polyhedron 2011, 30, 1906. https://doi.org/10.1016/j.poly.2011.04.029
  9. Ma, Y.; Zhou, N.; Chen, X.-P.; Cao, D.; Liao, D.-Z.; Yan, S.-P. J. Coord. Chem. 2009, 62, 3913. https://doi.org/10.1080/00958970903242515
  10. Le Bozec, H.; Le Bouder, T.; Maury, O.; Bondon, A.; Ledoux, I.; Deveau, S.; Zyss, J. Adv. Mater. 2001, 13, 1677. https://doi.org/10.1002/1521-4095(200111)13:22<1677::AID-ADMA1677>3.0.CO;2-J
  11. Le Bozec, H.; Le Bouder, T.; Maury, O.; Zyss, J. J. Opt. A: Pure Appl. Opt. 2002, 4, S189. https://doi.org/10.1088/1464-4258/4/6/351
  12. Duriska, M. B.; Neville, S. M.; Lu, J.; Iremonger, S. S.; Boas, J. F.; Kepert, C. J.; Batten, S. R. Angew. Chem. 2009, 121, 9081. https://doi.org/10.1002/ange.200903863
  13. Yang, W.; Greenaway, A.; Lin, X.; Matsuda, R.; Blake, A. J.; Wilson, C.; Lewis, W.; Hubberstey, P.; Kitagawa, S.; Champness, N. R.; Schroder, M. J. Am. Chem. Soc. 2010, 132, 14457. https://doi.org/10.1021/ja1042935
  14. Kumar, A.; Sun, S.-S.; Lees, A. J. Coord. Chem. Rev. 2008, 252, 922. https://doi.org/10.1016/j.ccr.2007.07.023
  15. Iki, N.; Ohta, M.; Tanaka, T.; Horiuchi, T.; Hoshino, H. New J. Chem. 2009, 33, 23. https://doi.org/10.1039/b816596c
  16. Han, S.; Kim, T.; Lough, A. J.; Kim, J. C. Inorg. Chim. Acta 2011, 370, 170. https://doi.org/10.1016/j.ica.2011.01.051
  17. Wan, C.-Q.; Mak, T. C. W. Cryst. Growth Des. 2011, 11, 832. https://doi.org/10.1021/cg101490a
  18. Biradha, K.; Zaworotko, M. J. J. Am. Chem. Soc. 1998, 120, 6431. https://doi.org/10.1021/ja974105m
  19. Moon, J. R.; Lough, A. J.; Yoon, Y. T.; Kim, Y. I.; Kim, J. C. Bull. Korean Chem. Soc. 2011, 32, 325. https://doi.org/10.5012/bkcs.2011.32.1.325
  20. Suh, M. P.; Cheon, Y. E.; Lee, E. Y. Coord. Chem. Rev. 2008, 252, 1007. https://doi.org/10.1016/j.ccr.2008.01.032
  21. Min, K. S.; Suh, M. P. Eur. J. Inorg. Chem. 2001, 449.
  22. Han, S.; Lough, A. J.; Kim, J. C. J. Coord. Chem. 2010, 63, 2069. https://doi.org/10.1080/00958972.2010.499456
  23. Han, S.; Lough, A. J.; Kim, J. C. Bull. Korean Chem. Soc. 2012, 33, 2381. https://doi.org/10.5012/bkcs.2012.33.7.2381
  24. Bosnich, B.; Poon, C. K.; Tobe, M. L. Inorg. Chem. 1965, 4, 1102. https://doi.org/10.1021/ic50030a003
  25. Kim, J. C.; Roh, J.; Lough, A. J. J. Chem. Cryst. 2007, 37, 615. https://doi.org/10.1007/s10870-007-9219-4
  26. Kim, J. C.; Lough, A. J. J. Chem. Cryst. 2005, 35, 535. https://doi.org/10.1007/s10870-005-2857-5
  27. Azcondo, M. T.; Ballester, L.; Gutierrez, A.; Perpinnan, M. F.; Amador, U.; Ruiz-Valero, C.; Bellitto, C. J. Chem. Soc., Dalton Trans. 1996, 3015.
  28. Cho, J.; Lough, A. J.; Kim, J. C. Inorg. Chim. Acta 2003, 342, 305. https://doi.org/10.1016/S0020-1693(02)01149-0
  29. Orpen, A. G.; Brammer, L.; Allen, F. H.; Kennard, O.; Watson, D. G.; Taylor, R., J. Chem. Soc., Dalton Trans. 1989, S1.
  30. Shin, J. W.; Yeo, S. M.; Min, K. S. Inorg. Chem. Commun. 2012, 22, 162. https://doi.org/10.1016/j.inoche.2012.05.051
  31. Kim, J. C.; Fettinger, J. C.; Kim, Y. I. Inorg. Chim. Acta 1999, 286, 67. https://doi.org/10.1016/S0020-1693(98)00382-X
  32. Oshio, H. Inorg. Chem. 1993, 32, 4123. https://doi.org/10.1021/ic00071a027
  33. Choi, K.-Y.; Kim, J. C.; Jensen, W. P.; Suh, I.-L.; Choi, S.-S. Acta Cryst. 1996, C52, 2166.
  34. Wickenden, A. E.; Krause, R. A. Inorg. Chem. 1965, 4, 404. https://doi.org/10.1021/ic50025a032
  35. Donlevy, T. M.; Gahan, L. R.; Hambley, T. W.; Hanson, G. R.; McMahon, K. L.; Stranger, R. Inorg. Chem. 1994, 33, 5131. https://doi.org/10.1021/ic00100a044
  36. Otwinowski, Z.; Minor, W. In Methods in Enzymology, Macromolucular Crystallography, Part A; Carter, C. W., Sweet, R. M., Eds.; Academic Press: London, 1997; Vol. 276, pp 307-326.
  37. Sheldrick, G. M. SHELXTL\PC V6.1, Bruker Analytical X-ray Systems, Madison, WI, 2001.

Cited by

  1. Macrocyclic Zinc(II) Coordination Polymers Constructed from Aromatic and Cyclohexane Dicarboxylate Ligands vol.59, pp.4, 2015, https://doi.org/10.5012/jkcs.2015.59.4.336
  2. Synthesis, Crystal Structure, and Spectroscopic Properties of Cu(II) Complex with 14-Membered Hexaazamacrocyclic Ligands vol.46, pp.5, 2016, https://doi.org/10.1007/s10870-016-0649-8
  3. Macrocyclic Copper(II) Complex with Unusual Involvement of btc4- (btc = 1,2,4,5-Benzenetetracarboxylate Ion) Ligand vol.63, pp.3, 2013, https://doi.org/10.5012/jkcs.2019.63.3.209
  4. Supramolecules Self-assembled by Nickel(II) Hexaazamacrocycles Bearing Imidazole Pendants vol.64, pp.6, 2013, https://doi.org/10.5012/jkcs.2020.64.6.438