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Molecular complexation of some amino acids and triglycine with 18-crown-6 ether in H2O-EtOH solvents at 298.15 K

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Abstract

The influence of composition of H2O-EtOH solvent on the reaction of formation of a molecular complex of 18-crown-6 ether (18C6) with triglycine (3Gly) has been studied at 298.15 K by a thermochemical method. The standard thermodynamic parameters (Δr G°, Δr H°, and TΔr S°) of the reaction of [3Gly18C6] complex formation in water-ethanol (H2O-EtOH) solvents having an EtOH mole fraction of 0.0, 0.1, 0.15, 0.2, 0.25, 0.30, and 0.50 have been calculated from the data of calorimetric measurements performed on a TAM III titration microcalorimeter. It has been found that an increase in EtOH concentration in the mixed solvent results in an increase in stability of [3Gly18C6] and in an enhancement in exothermicity of its formation reaction. The water-ethanol solvent has an analogous effect on the stability and energetics of the reactions of formation of molecular complexes of 18C6 with glycine, D,L-alanine, and L-phenylalanine.

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References

  1. J.-M. Lehn, Supramolecular Chemistry: Concepts and Perspectives (Wiley/VCH, Weinheim, 1995; Nauka, Novosibirsk, 1998).

    Book  Google Scholar 

  2. J. W. Steed and J. L. Atwood, Supramolecular Chemistry, 1st Ed. (CRC Press, 2004; IKTs Akademkniga, Moscow, 2007).

    Google Scholar 

  3. V. A. Shormanov and V. A. Sharnin, Advances and Topics in the Solvation Theory: Structure and Thermodynamic Aspects, Ed. by A.M.. Kutepov (Nauka, Moscow, 1998) [in Russian].

  4. V. A. Sharnin, Izv. Vyssh. Uchebn. Zaved.: Khim. Khim. Tekhnol. 48(7), 44 (2005).

    CAS  Google Scholar 

  5. V. A. Sharnin, Zh. Obshch. Khim. 69, 1421 (1999).

    Google Scholar 

  6. E. Matteoli, L. Lepori, T. R. Usacheva, and V. A. Sharnin, J. Therm. Anal. Calorim. 97, 811 (2009).

    Article  CAS  Google Scholar 

  7. T. R. Usacheva, V. A. Sharnin, and E. Matteoli, Russ. J. Phys. Chem. A 85, 1898 (2011).

    Article  CAS  Google Scholar 

  8. T. R. Usacheva, I. A. Kuz’mina, V. A. Sharnin, et al., Russ. J. Phys. Chem. A 85, 948 (2011).

    Article  CAS  Google Scholar 

  9. T. R. Usacheva, V. A. Sharnin, I. V. Chernov, and E. Matteoli, J. Therm. Anal. Calorim. doi 10.1007/s10973-012-2625-7.

  10. T. R. Usacheva, I. A. Kuz’mina, V. A. Sharnin, et al., Russ. J. Phys. Chem. A 86, 1064 (2012).

    Article  CAS  Google Scholar 

  11. T. R. Usacheva, I. A. Kuz’mina, V. A. Sharnin, et al., Russ. J. Phys. Chem. A 86, 36 (2012).

    Article  CAS  Google Scholar 

  12. T. R. Usacheva, V. A. Sharnin, I. V. Chernov, et al., Chem. Phys. Lett. 543, 155 (2012).

    Article  CAS  Google Scholar 

  13. O. V. Kulikov and I. V. Terekhova, Koord. Khim. 24, 395 (1998).

    Google Scholar 

  14. A. F. de Namor, M. C. Ritt, D. F. V. Lewis, et al., Pure Appl. Chem. 63, 1435 (1991).

    Article  Google Scholar 

  15. A. F. de Namor, M. C. Ritt, M. J. Schwing-Weill, et al., J. Chem. Soc., Faraday Trans. 87, 3231 (1991).

    Article  Google Scholar 

  16. H.-J. Buschmann and L. Mutihac, J. Inclus. Phenom. Macrocycl. Chem. 42, 193 (2002).

    Article  CAS  Google Scholar 

  17. M. Hiraoka, Crown Compounds: Their Characteristics and Applications (Kodansha, Tokyo, 1982).

    Google Scholar 

  18. W. Zielenkewicz, O. V. Kulikov, and G. A. Krestov, J. Solution Chem. 24, 1155 (1995).

    Article  Google Scholar 

  19. Y. Nozaki and C. Tanford, J. Biol. Chem. 246, 2211 (1971).

    CAS  Google Scholar 

  20. V. P. Vasil’ev, V. A. Borodin, and E. V. Kozlovskii, Computers in Chemical Analytical Comptutations (Vysshaya Shkola, Moscow, 1993) [in Russian].

    Google Scholar 

  21. G. Brookes and L. Pettit, J. Chem. Soc., Dalton Trans., No. 20, 2106 (1975).

    Google Scholar 

  22. A. Kaneda and A. Martell, J. Coord. Chem. 4(3), 137 (1975).

    Article  CAS  Google Scholar 

  23. C. Agoston, T. Jankowska, and I. Sovago, J. Chem. Soc., Dalton Trans., No. 18, 3295 (1999).

    Google Scholar 

  24. V. G. Badelin, V. P. Barannikov, G. N. Tarasova, et al., Russ. J. Phys. Chem. A 86, 40 (2012).

    Article  CAS  Google Scholar 

  25. V. A. Borodin, E. V. Kozlovskii, and V. P. Vasil’ev, Zh. Neorg. Khim. 27, 2169 (1982).

    CAS  Google Scholar 

  26. G. R. Hedwig and H. Hoiland, J. Chem. Thermodyn. 25, P. 3349 (1993).

    Article  Google Scholar 

  27. I. F. Reading and G. R. Hedwig, J. Chem. Soc., Faraday Trans. 86, 3177 (1990).

    Article  Google Scholar 

  28. O. V. Kulikov and G. A. Krestov, Pure Appl. Chem. 67, 1103 (1995).

    Article  CAS  Google Scholar 

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Original Russian Text © T.R. Usacheva, Fam Tkhi Lan, V.A. Sharnin, A. Baranski, 2013, published in Zhurnal Neorganicheskoi Khimii, 2013, Vol. 58, No. 10, pp. 1409–1413.

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Usacheva, T.R., Lan, F.T., Sharnin, V.A. et al. Molecular complexation of some amino acids and triglycine with 18-crown-6 ether in H2O-EtOH solvents at 298.15 K. Russ. J. Inorg. Chem. 58, 1264–1268 (2013). https://doi.org/10.1134/S0036023613100239

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  • DOI: https://doi.org/10.1134/S0036023613100239

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