Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Three 1-(4-Hydroxyphenyl)-1H-1,2,4-triazole-based Cd(II) Coordination Polymers Directed by Aromatic Polycarboxylate Coligands

  • Yang, En-Cui (College of Chemistry & Life Science, Key Laboratory of Molecular Structure and Materials Performance, Tianjin Normal University) ;
  • Jia, Fang (College of Chemistry & Life Science, Key Laboratory of Molecular Structure and Materials Performance, Tianjin Normal University, Tianjin 300387, China) ;
  • Wang, Xiu-Guang (College of Chemistry & Life Science, Key Laboratory of Molecular Structure and Materials Performance, Tianjin Normal University) ;
  • Zhao, Xiao-Jun (College of Chemistry & Life Science, Key Laboratory of Molecular Structure and Materials Performance, Tianjin Normal University)
  • Published : 2008.11.20
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References

  1. Ouellette, W.; Hudson, B. S.; Zubieta, J. Inorg. Chem. 2007, 46, 4887 https://doi.org/10.1021/ic062269a
  2. Ouellette, W.; Prosvirin, A. V.; Chieffo, V.; Dunbar, K. R.; Hudson, B. S.; Zubieta, J. Inorg. Chem. 2006, 45, 9346 https://doi.org/10.1021/ic061102e
  3. Ouellette, W.; Yu, M. H.; O'Connor, C. J.; Hagrman, D.; Zubieta, J. Angew. Chem. Int. Ed. 2006, 45, 3497 https://doi.org/10.1002/anie.200504128
  4. Ouellette, W.; Galán- Mascarós, J. R.; Dunbar, K. R.; Zubieta, J. Inorg. Chem. 2006, 45, 1909
  5. Liu, J. C.; Fu, D. G.; Zhuang, J. Z.; Duan, C. Y.; You, X. Z. J. Chem. Soc. Dalton Trans. 1999, 2337
  6. Abramovitch, R. A.; Gibson, H. H.; Olivella, S. J. Org. Chem. 2001, 66, 1242 https://doi.org/10.1021/jo001382u
  7. Asaji, T.; Sakai, H.; Nakamura, D. Inorg. Chem. 1983, 22, 202 https://doi.org/10.1021/ic00144a005
  8. Ferrer, S.; Haasnoot, J. G.; Reedijk, J.; Muller, E.; Biagini Cindi, M.; Lanfranchi, M.; Manotti Lanfredi, A. M.; Rilas, J. Inorg. Chem. 2000, 39, 1859 https://doi.org/10.1021/ic981393u
  9. Shakirova, O. G.; Virovets, A. V.; Naumov, D. Y.; Shvedenkov, Y. G.; Elochina, V. N.; Lavrenova, L. G. Inorg. Chem. Commun. 2002, 5, 690 https://doi.org/10.1016/S1387-7003(02)00524-5
  10. Foces-foces, C.; Cabildo, P.; Claramunt, R. M.; Elguero, J. Acta Cryst. 1999, C55, 1160
  11. Thomann, M.; Kahn, J. O.; Guilhem, J.; Varreta, F. Inorg. Chem. 1994, 33, 6029 https://doi.org/10.1021/ic00104a010
  12. Gulich, P.; Garcia, Y.; Goodwin, H. A. Chem. Soc. Rev. 2000, 29, 419 https://doi.org/10.1039/b003504l
  13. Lider, E. V.; Peresypkina, E. V.; Smolentsev, A. I.; Elokhina, V. N.; Yaroshenko, T. I.; Virovets, A. V.; Ikorskii, V. N.; Lavrenova, L. G. Polyhedron 2007, 26, 1612 https://doi.org/10.1016/j.poly.2006.11.051
  14. Liu, B.; Guo, G.-C.; Huang, J.-S. J. Solid State Chem. 2006, 179, 3136 https://doi.org/10.1016/j.jssc.2006.05.046
  15. Liu, B.; Li, B.; Zhang, X.-C. Bull. Korean Chem. Soc. 2006, 27, 1677 https://doi.org/10.5012/bkcs.2006.27.10.1677
  16. Zhang, X.-C.; Chen, Y.-H.; Liu, B. Bull. Korean Chem. Soc. 2008, 29, 511 https://doi.org/10.5012/bkcs.2008.29.2.511
  17. Lavrenova, L. G.; Ikorskii, V. N.; Sheludyakova, L. A.; Naumov, D. Yu.; Boguslavskii, E. G. Russian J. Coord. Chem. 2004, 30, 413 https://doi.org/10.1023/B:RUCO.0000030162.64191.66
  18. Haasnoot, J. G. Coord. Chem. Rev. 2000, 200, 131 https://doi.org/10.1016/S0010-8545(00)00266-6
  19. Bruker AXS SAINT Software Reference Manual; Madison, WI, 1998
  20. Sheldrick, G. M. SADABS: Program for Empirical Absorption Correction of Area Detector Data; University of Gottingen: Germany, 1996
  21. Sheldrick, G. M. SHELXL-97, Program for X-ray Crystal Structure Refinement; Gottingen University: Gottingen, Germany, 1997
  22. Sheldrick, G. M. SHELXS-97, Program for X-ray Crystal Structure Solution; Gottingen University: Gottingen, Germany, 1997
  23. Deacon, G. B.; Phillips, R. J. Coord. Chem. Rev. 1980, 33, 227 https://doi.org/10.1016/S0010-8545(00)80455-5
  24. Bellamy, L. J. The Infrared Spectra of Complex Molecules; Wiley: New York, 1958
  25. Ouellette, W.; Prosvirin, A. V.; Valeich, J.; Dunbar, K. R.; Zubieta, J. Inorg. Chem. 2007, 46, 9067 https://doi.org/10.1021/ic700790h
  26. Zhai, Q.-G.; Lu, C.-Z.; Wu, X.-Y.; Batten, S. R. Cryst. Growth Des. 2007, 7, 2332 https://doi.org/10.1021/cg070593q
  27. Lippert, B. Coord. Chem. Rev. 2000, 200, 487 https://doi.org/10.1016/S0010-8545(00)00260-5
  28. Bugella- Altamirano, E.; Choquesillo-Lazarte, D.; Gonzalez-Perez, J. M.; Sanchez-Moreno, M. J.; Maain-Sanchez, R.; Martin-Ramos, J. D.; Covelo, B.; Carballo, R.; Castineiras, A.; Niclos-Gutierrez, J. Inorg. Chim. Acta 2002, 339, 160 https://doi.org/10.1016/S0020-1693(02)00920-9
  29. Marzotto, A.; Clemente, D. A.; Ciccarese A.; Valle, G. J. Crystallogr. Spectrosc. Res. 1993, 23, 119 https://doi.org/10.1007/BF01195446
  30. Gorter, S.; Engelfriet, D. W. Acta Crystallogr. Sect. B 1981, 37, 1214 https://doi.org/10.1107/S0567740881005530
  31. Cebrian-Losantos, B.; Krokhin, A. A.; Stepanenko, I. N.; Eichinger, R.; Jakupec, M. A.; Arion, V. B.; Keppler, B. K. Inorg. Chem. 2007, 46, 5023 https://doi.org/10.1021/ic700405y
  32. Park, H.; Britten, J. F.; Mueller, U.; Lee, J. Y.; Li, J.; Parise, J. B. Chem. Mater. 2007, 19, 1302 https://doi.org/10.1021/cm0623918
  33. Park, H.; Krigsfeld, G.; Parise, J. B. Cryst. Growth Des. 2007, 7, 736 https://doi.org/10.1021/cg060741x

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