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Macrocyclic Copper(II) Complex with Unusual Involvement of btc4- (btc = 1,2,4,5-Benzenetetracarboxylate Ion) Ligand

  • Kim, Taeyeong (Department of Chemistry, Pukyong National University) ;
  • Kim, Ju Chang (Department of Chemistry, Pukyong National University)
  • Received : 2019.02.15
  • Accepted : 2019.02.21
  • Published : 2019.06.20

Abstract

Keywords

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Scheme 1. Molecular structures of L, L1, L2, and H4btc.

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Figure 1. Structure of [Cu2(L1)2(μ-btc4-)]2- anion with atomlabeling scheme. Hydrogen atoms other than those participating in hydrogen bonding are omitted for clarity. Cu1-N1, 2.0613(17); Cu1-N2, 2.0213(16); Cu1-N3, 2.0479(17); Cu1-N4, 2.0105(16); Cu1-O1, 2.3742(14); C21-O1, 1.255(2); C21-O2, 1.262(3); C25-O3, 1.260(6); C25-O4, 1.247(6); N1-Cu1-N2, 84.26(7); N1-Cu1-N4, 93.06(6); N2-Cu1-N3, 96.59(7); N3-Cu1-N4, 85.15(7); N1-Cu1-O1, 100.03(6); N2-Cu1-O1, 95.39(6); N3-Cu1-O1, 87.25(6); N4-Cu1-O1, 92.11(6). Symmetry codes: #1 -x+1,-y+1,-z #2 -x+1,-y+2,-z.

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Figure 2. View of 1D supramolecule formed with hydrogen bonding interactions between [Cu(L1)(H2O)2]2+ cation and [Cu2(L1)2(μ- btc4-)]2- anion.

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Figure 3. View of hydrogen bonding interactions between [Cu(L1) (H2O)2]2+ cation and [Cu2(L1)2(μ-btc)]2- anion.

Table 1. Crystal data and structure refinement for 1

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References

  1. Kitagawa, S.; Kitaura, R.; Noro, S.-I. Angew. Chem. Int. Ed. 2004, 43, 2334. https://doi.org/10.1002/anie.200300610
  2. Lee, E. Y.; Suh, M. P. Angew. Chem. Int. Ed. 2004, 43, 2798. https://doi.org/10.1002/anie.200353494
  3. Choi, H. J.; Lee, T. S.; Suh, M. P. Angew. Chem. Int. Ed. 1999, 38, 1405. https://doi.org/10.1002/(SICI)1521-3773(19990517)38:10<1405::AID-ANIE1405>3.0.CO;2-H
  4. Clegg, W.; Holcroft, J.; Martin, N. C. Cryst. Eng. Comm 2015, 17, 2857. https://doi.org/10.1039/C5CE00470E
  5. Rochon, F. D.; Massarweh, G. Inorg. Chim. Acta 2001, 314, 163. https://doi.org/10.1016/S0020-1693(01)00307-3
  6. Rochon, F. D.; Massarweh, G. Inorg. Chim. Acta 2000, 304, 190. https://doi.org/10.1016/S0020-1693(00)00086-4
  7. 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
  8. Kim, J. C. Bull. Korean Chem. Soc. 2015, 36, 2131. https://doi.org/10.1002/bkcs.10375
  9. Kim, T.; Lough, A. J.; Kim, J. C. Bull. Korean Chem. Soc. 2013, 34, 1913. https://doi.org/10.5012/bkcs.2013.34.6.1913
  10. Kwag, J. S.; Lough, A. J.; Kim, J. C. J. Chem. Crystallogr. 2011, 41, 1494. https://doi.org/10.1007/s10870-011-0129-0
  11. Shi, Q.; Cao, R.; Sun, D.-F.; Hong, M.-C.; Liang, Y.-C. Polyhedron 2001, 20, 3287. https://doi.org/10.1016/S0277-5387(01)00945-7
  12. Cho, J.; Lough, A. J. Kim, J. C. Inorg. Chim. Acta 2003, 342, 305. https://doi.org/10.1016/S0020-1693(02)01149-0
  13. Kang, S.-G.; Kweon, J. K.; Jung, S.-K. Bull. Korean Chem. Soc. 1991, 12, 483.
  14. Lee, J. Y.; Kang, S.-G.; Kwak, C.-H. Inorg. Chim. Acta 2015, 430, 61. https://doi.org/10.1016/j.ica.2015.02.028
  15. Kim, H.; Lee, J. Y.; Kang, S.-G.; Kwak, C.-H. Bull. Korean Chem. Soc. 2014, 35, 305. https://doi.org/10.5012/bkcs.2014.35.1.305
  16. Kang, S.-G.; Jeong, J. H. Bull. Korean Chem. Soc. 2003, 24, 393. https://doi.org/10.5012/bkcs.2003.24.3.393
  17. Kim, J. C.; Cho, J. Kim, H.; Lough, A. J. Chem. Commun. 2004, 1796.
  18. 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
  19. Moon, J. R.; Lough, A. J.; Yoon, Y. T.; Kim, Y. I.; Kim, J. C. Inorg. Chim. Acta 2010, 363, 2682. https://doi.org/10.1016/j.ica.2010.04.033
  20. 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
  21. Kwag, J. S.; Jeong, M. H.; Lough, A. J.; Kim, J. C. Bull. Korean Chem. Soc. 2010, 31, 2069. https://doi.org/10.5012/bkcs.2010.31.7.2069
  22. Kim, J. C.; Lough, A. J.; Jo, H. Inorg. Chem. Commun. 2002, 5, 616. https://doi.org/10.1016/S1387-7003(02)00506-3
  23. Kim, J. C.; Roh, J.; Lough, A. J. J. Chem. Crystallogr. 2007, 37, 615. https://doi.org/10.1007/s10870-007-9219-4
  24. Hunter, T. M.; McNae, I. W.; Liang, X.; Bella, J.; Parsons, S.; Walkinshaw, M. D.; Sadler, P. J. Proc. Natl. Acad. Sci. USA 2005, 102, 2288. https://doi.org/10.1073/pnas.0407595102
  25. Jo, H.; Lough, A. J.; Kim, J. C. Inorg. Chim. Acta 2005, 358, 1274. https://doi.org/10.1016/j.ica.2004.10.025
  26. Kim, J. C.; Lough, A. J.; Kim, H. Inorg. Chem. Commun. 2002, 5, 771. https://doi.org/10.1016/S1387-7003(02)00556-7
  27. Kim, J. C.; Jo, H.; Lough, A. J.; Cho, J.; Lee, U.; Pyun, S. Y. Inorg. Chem. Commun. 2003, 6, 474. https://doi.org/10.1016/S1387-7003(03)00016-9
  28. Tasker, P. A.; Sklar, L. J. Cryst. Mol. Struct. 1975, 5, 329. https://doi.org/10.1007/BF01270621
  29. Otwinowski, Z.; Minor, W. In Methods in Enzymology, Macromolucular Crystallography, Part A; Carter, C. W., Sweet, R. M., Eds.; Academic Press: London, 1997; pp 307-326.
  30. Sheldrick, G. M. SHELXTL\PC V6.1, Bruker Analytical X-ray Systems, Madison, WI (2001).