DOI QR코드

DOI QR Code

Endo- and Exo-Coordinated Mercury(II) Complexes of O3S2 Macrocycles: Effect of Dibenzo-Substituents on Coordination Mode

  • Lee, Ji-Eun (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Kim, Hyun-Jee (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Lee, So-Young (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Lee, Jai-Young (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Jin, Yong-Nu (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University) ;
  • Lee, Shim-Sung (Department of Chemistry (BK21) and Research Institute of Natural Science, Gyeongsang National University)
  • Published : 2007.11.20

Abstract

The reactions of mercury(II) chloride with O3S2-donor macrocyclic ligands with (L1) and without (L2) dibenzosubunit afforded respective exo- (1) and endo-coordinated (2) complexes depending on the ring rigidity of the ligands. From the X-ray crystal structures and comparative NMR studies for the complexes 1 and 2, it is confirmed that the resulting species with different coordination modes exist not only in solid state but also in solution state.

Keywords

References

  1. Lindoy, L. F. The Chemistry of Macrocyclic Complexes; Cambridge University Press: Cambridge, U. K., 1989
  2. Lehn, J.-M. Supramolecular Chemistry, Concept and Perspectives; VCH: Weinheim, Germany, 1995
  3. Jin, Y.; Yoon, I.; Seo, J.; Lee, J.-E.; Moon, S.-T.; Kim, J.; Han, S. W.; Park, K.-M.; Lindoy, L. F.; Lee, S. S. Dalton Trans. 2005, 788
  4. Yoon, I.; Seo, J.; Lee, J.-E.; Song, M. R.; Lee, S. Y.; Choi, K. S.; Jung, O.-S.; Park, K.-M.; Lee, S. S. Dalton Trans. 2005, 2352
  5. Park, K.-M.; Yoon, I.; Seo, J.; Lee, J.-E.; Kim, J.; Choi, K. S.; Jung, O.-S.; Lee, S. S. Cryst. Growth Des. 2005, 5, 1707 https://doi.org/10.1021/cg050220u
  6. Seo, J.; Yoon, I.; Lee, J.-E.; Song, M. R.; Lee, S. Y.; Park, S. H.; Kim, T. H.; Park. K.-M.; Kim, B. G.; Lee, S. S. Inorg. Chem. Commun. 2005, 8, 916 https://doi.org/10.1016/j.inoche.2005.07.006
  7. Lee, J.-E.; Jin, Y.; Seo, J.; Yoon, I.; Song, M. R.; Lee, S. Y.; Park, K.-M.; Lee, S. S. Bull. Korean Chem. Soc. 2006, 27, 203 https://doi.org/10.5012/bkcs.2006.27.2.203
  8. Yoon, I.; Seo, J.; Lee, J.-E.; Park, K.-M.; Kim, J. S.; Lah, M. S.; Lee, S. S. Inorg. Chem. 2006, 45, 3487 https://doi.org/10.1021/ic060005i
  9. Seo, J.; Lee, J.-E.; Song, M. R.; Lee, S. Y.; Yoon, I.; Park, K.-M.; Kim, J.; Jung, J. H.; Park, S. B.; Lee, S. S. Inorg. Chem. 2006, 45, 952 https://doi.org/10.1021/ic051764o
  10. Park, S. B.; Yoon, I.; Seo, J.; Kim, H. J.; Kim, J. S.; Lee, S. S. Bull. Korean Chem. Soc. 2006, 27, 713 https://doi.org/10.5012/bkcs.2006.27.5.713
  11. Lee, Y. H.; Lee, S. S. J. Inclusion Phenom. 2001, 39, 235 https://doi.org/10.1023/A:1011116404850
  12. Song, M. R.; Lee, J.-E.; Lee, S. Y.; Seo, J.; Park, K.-M.; Lee, S. S. Inorg. Chem. Commun. 2006, 9, 75 https://doi.org/10.1016/j.inoche.2005.10.009
  13. Von Burg, R. J. Appl. Toxicol. 1995, 15, 483 https://doi.org/10.1002/jat.2550150610
  14. Magos, L. Met. Ions Biol. Syst. 1997, 34, 321
  15. Wolfe, M. F.; Schwarzbach, S.; Sulaiman, R. A. Environ. Toxicol. Chem. 1998, 17, 146 https://doi.org/10.1897/1551-5028(1998)017<0146:EOMOWA>2.3.CO;2
  16. Marchand, A. P.; Cal, D.; Mlinaric-Majerski, K.; Ejsmont, K.; Watson, W. H. J. Chem. Cryst. 2002, 32, 447
  17. Caltagirone, C.; Bencini, A.; Demartin, F.; Devillanova, F. A.; Garau, A.; Isaia, F.; Lippolis, V.; Mariani, P.; Papke, U.; Tei, L.; Verani, G. Dalton Trans. 2003, 901
  18. Afshar, S.; Marcus, S. T.; Gahan, L. R.; Hambley, T. W. Aust. J. Chem. 1999, 52, 1 https://doi.org/10.1071/C98096
  19. Byriel, K. A.; Gahan, L. R.; Kennard, C. H. L.; Sunderland, C. T. J. Chem. Soc., Dalton Trans. 1993, 625
  20. Bebout, D. C.; Bush II, J. F.; Crahan, K. K.; Kastner, M. E.; Parrish, D. A. Inorg. Chem. 1998, 37, 4641 https://doi.org/10.1021/ic980296y
  21. Cecconi, F.; Ghilardi, C. A.; Midollini, S.; Orlandini, A. Inorg. Chim. Acta 1998, 269, 274 https://doi.org/10.1016/S0020-1693(97)05805-2
  22. Chessa, G.; Marangoni, G.; Pitteri, B.; Bertolasi, V.; Ferretti, V.; Gilli, G. J. Chem. Soc., Dalton Trans. 1990, 915
  23. Bruker SMART and SAINT: Area Detector Control and Integration Software Ver. 5.0; Bruker Analytical X-ray Instruments: Madison, Wisconsin, 1998
  24. Sheldrick, G. M. SADABS: Empirical Absorption and Correction Software; University of Gottingen: Gottingen, Germany, 1999
  25. Bruker SHELXTL: Structure Determination Programs Ver. 5.16; Bruker Analytical X-ray Instruments: Madison, Wisconsin, 1998

Cited by

  1. Endo- and Exocyclic Supramolecular Complexes of Mixed-Donor Macrocycles via [1:1] and [2:2] Cyclizations vol.52, pp.15, 2013, https://doi.org/10.1021/ic400247q
  2. Mercury(II) Halide and Copper(I) Iodide Complexes of Double-Tweezer Ligand with Thiocyclohexyl End-Group vol.30, pp.4, 2007, https://doi.org/10.5012/bkcs.2009.30.4.961