DOI QR코드

DOI QR Code

Conductometric Behavior of Univalent Cation-Podand Complexes in Methanol

  • Kim, Dae-Yeon (Department of Chemistry, Gyeongsang National University) ;
  • Jung, Jong-Hwa (Department of Chemistry, Gyeongsang National University) ;
  • Chun, Jae-Sang (Korea Research Institute of Chemical Technology) ;
  • Lee, Shim-Sung (Department of Chemistry, Gyeongsang National University)
  • Published : 1994.11.20

Abstract

The stability constants, log K of the 1 : 1 complexation for IA ions, $Ag^+$, and $Tl^+$ with a series of podands having different aromatic end-groups (I-IV) have been determined conductometrically in methanol at 25.0 $^{\circ}$C. Exceptionally the equivalent conductivity, ${\lambda}_{eq}\;of\;Li^+\;and\;Na^+$ were increased by the addition of I, because the complexed ions are less mobile than solvated ions. The order of log K values for I was $Ag^+{\gg}Tl^+>K^+>Na^+>Rb^+>Cs6+>Li^+$. The log K sequence of the podands for the certain cations was I>II>III${\geq}$IV. And every podands except IV showed the maximum selectivity for $Ag^+$ among the cations. These results were discussed in terms of the aromatic end-group effects, such as hetero-donor atoms or conformational changes by ${\pi}-{\pi}$ stacking interactions. The detailed conformations of ${\pi}-{\pi}$ stacking were also discussed by the observations of upfield shifts of some aromatic protons upon complexation from $^1H$ NMR spectra.

Keywords

References

  1. Biomembranes: Molecular Stucture and Funtion Gennis, R. B.
  2. Macrocyclic Polyether Syntheses Gokel, G. W.;Korzeniowski, S. H.
  3. Angew. Chem. Int. Ed. Engl. v.31 Seel, C.;Vogtle, F.
  4. Tetrahedron Lett. Weber, E.;Vogtle, F.
  5. J. Am. Chem. Soc. v.101 Tummler, B.;Maass, G.;Vogtle, F.;Sieger, H.;Heimann, U.;Weber, E.
  6. Chem. Rev. v.91 Izatt, R. M.;Pawlak, K.;Bradshaw, J. S.
  7. Thermochim. Acta v.107 Buschmann, H-J
  8. Thermochim. Acta Lee, S. S.;Jung, J. H.;Yu, S. H.;Cho, M. H.
  9. Bull. Kor. Chem. Soc. v.13 Lee, S. S.;Jung, J. H.;Cho, S. B.;Kim, J. S.;Kim, J.;Kim, S.-J.
  10. J. Am. Chem. Soc. v.101 Izatt, R. M.;Lamb, J. D.;Izatt, N. E.;Rossiter, Jr., B. E.;Christensen, J. J.;Haymore, B. L.
  11. J. Solution Chem. v.4 Cohen, Y. M.;Popov, A. I.
  12. J. Solution Chem. v.6 Dewitte, W. J.;Liu, L.;Mei, E.;Dye, J. L.;Popov, A. I.
  13. Inorganic Chim. Acta v.195 Buschmann, H.-J.
  14. Cation Binding by Macrocycles Inoue, Y.;Liu, Y.;Hakushi, T.;Inoue, Y.(ed.);Gokel, G. W.(ed.)
  15. Cation Binding by Macrocycles Takeda, Y.;Inoue, Y.(ed.);Gokel, G. W.(ed.)
  16. Polym. Prepr., Am. Chem. Soc., Div. Polym. Chem. v.20 Ono, K.;Konami, H.;Murakami, K.
  17. 71st Annual Meeting of Korean Chemical Society Lee, S. S.;Kim, D. Y.;Jung, J. H.;Kim, S.-J.
  18. J. Incl. Phenom. v.10 Wakita, R.;Miyakoshi, M.;Nakatsuguji, Y.;Okahara, M.
  19. Bull. Kor. Chem. Soc. Jung, J. H.;Lee, S. S.
  20. The Chemist's Companion Gordon, A. J.;Ford, R. A.
  21. Bull. Chem. Soc. Jpn. v.53 Takeda, Y.;Yano, H.;Ishibashi, M.;Isozumi, H.
  22. Laboratory Automization Using the IBM PC Gates, S. C.;Becker, J.
  23. J. Chem. Edu. v.48 Dye, J. L.;Nicely, V. A.
  24. J. Phys. Chem. v.84 Hopkins, Jr., H. P.;Norman, A. B.
  25. Bull. Kor. Chem. Soc. v.11 Lee, S. S.;Park, S. O.;Jung, J. H.;Lee, B. Y.
  26. J. Am. Chem. Soc. v.85 Pearson, R. G.
  27. J. Incl. Phenom. v.13 Zhu, C. Y.;Izatt, R. M.;Bradshaw, J. S.;Dalley, N. K.
  28. Inorg. Chem. v.19 Lindoy, S. F.;Lip, H. C.;Rea, J. H.;Smith, R. H.;Tasker, P. A.
  29. Angew. Chem. Int. Ed. Engl. v.17 Sieger, H.;Vogtle, H.