SciELO - Scientific Electronic Library Online

 
vol.53 número4Rapid and Sensitive Spectrophotometric Method for the Determination of the Trace Amount of Thallium (III) in Water and Urine Samples by New Oxidative Coupling ReactionReactions of Vinylcyclopropane and Bicyclopropyl Compounds With Maleic Anhydride índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Journal of the Mexican Chemical Society

versão impressa ISSN 1870-249X

J. Mex. Chem. Soc vol.53 no.4 Ciudad de México Out./Dez. 2009

 

Article

 

Crown Ether Ditopic Receptors for Ammonium Salts with High Affinity for Amino Acid Ester Salts

 

Sharon Rosete–Luna, Felipe Medrano, Margarita I. Bernal–Uruchurtu, and Carolina Godoy–Alcántar*

 

Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos, 62209 Cuernavaca, Morelos, México. Tel/Fax: +52 777329 7997. *Responsible author: cga@uaem.mx

 

Received August 13, 2009
Accepted November 19, 2009

 

Abstract

Two bis crown ether receptors were synthesized and tested as host molecules for protonated forms of alkyl amines and amino acid esters. Molecular recognition studies were conducted in CH2Cl2:MeOH (92:8) by spectrophotometric UV/Vis titrations and by spectrometric 1H NMR titrations in CDCl3. The calculated binding constants are in the range 102–105 M–1. A high affinity for L–amino acid methyl ester derivatives was found. A theoretical study at the DFT level of the synthesized receptor and some analog ligands with three different ammonium ions helps to rationalize the experimentally found trends.

Key words: Ditopic Receptors, Binding Constant; Crown Ethers, Alkyl Ammonium, Amino Acid.

 

Resumen

En este trabajo se sinterizaron dos receptores del tipo bis eter corona y fueron estudiados como moléculas anfitrión de alquilaminas y ésteres de aminoácidos protonados. Se realizaron estudios de reconocimiento molecular por titulaciones espectrofotométricas UV/Vis en CH2Cl2:MeOH (92:8) y por titulaciones espectrométricas de RMN 1H en CDCl3. Las constantes de enlace calculadas están en el intervalo 102–105 M–1. Se encontró una alta afinidad por los ésteres metílicos de los L–aminoácidos estudiados. Un estudio teórico a nivel DFT de los receptores sinterizados y algunos ligandos análogos con tres diferentes iones amonio permite explicar las tendencias experimentales encontradas.

Palabras clave: Receptores ditópicos, constante de enlace, éteres corona, alquilamonio, aminoácido.

 

DESCARGAR ARTÍCULO EN FORMATO PDF

 

Acknowledgements

We thank Professor A. K. Yatsimirsky for the advice and fruitful discussion of the results. SRL thanks CONACyT for the Ph. D. Fellowship. This work was supported by CONACyT, projects 39574-Q and 60747.

 

References

1. Guy, P. A.; Gremaud, E.; Richoz, J.; Turesky, R. J. J. Chromatogr., A 2000, 883, 89–102.         [ Links ]

2. (a) Ohgaki, H.; Takayama, S.; Sugimura, T. Mutat. Res. 1991, 259, 399–410.         [ Links ] (b) Wakabayashi, K.; Nagao, M.; Esumi, H.; Sugimura, T. Cancer Res.1992, 52, 2092S–2098S.         [ Links ]

3. (a) Sutherland, I. O. Pure Appl. Chem. 1989, 61, 1547–1554.         [ Links ] (b) Voyer, N.; Lamothe, J. Tetrahedron 1995, 51, 9241–9284.         [ Links ] (c) Gokel, G. W.; Abel, E. Comprehensive Supramolecular Chemistry; Vol. 1, Elsevier: Oxford, England, 1996;         [ Links ].(d) Gokel, G. W.; Leevy, W. M.; Weber, M. E. Chem. Rev. 2004, 104, 2723–2750.         [ Links ]

4. (a) Hayashi, T.; Nonogushi, M.; Aya, T.; Ogoshi, H. Tetrahedron Lett.1997, 38, 1603.         [ Links ] (b) Ema, T.; Misawa, S.; Nemugaki, S.; Sakai, T.; Utaka, M. Chem. Lett. 1997, 487–488.         [ Links ]

5. (a)Tsubacki, K.; Kusumoto, T.; Hayashi, N.; Nuruzzaman, M.; Fuji, K. Org. Lett. 2002, 4, 2313–2316.         [ Links ] (b) de Silva, A. P.; Sandanayake, K. R. A. S. Angew. Chem. Int. Ed. Engl. 1990, 29, 1173–1175.         [ Links ]

6. (a) Feuster, E. K.; Glass, T. E. J. Am. Chem. Soc. 2003, 125, 16174–16175.         [ Links ](b) Mohr, G. J. Chem. Eur. J. 2004, 10, 1082–1090.         [ Links ]

7. (a) Zimmerman, S. C.; Wendland, M. S.; Rakow, N. A.; Zharov, I.; Suslick, K. S. Nature 2002, 418, 399–402.         [ Links ] (b) Mertz, E.; Zimmerman, S. C. J. Am. Chem. Soc. 2003, 125, 3424–3425.         [ Links ]

8. Colera, M.; Costero, A. M.; Gaviña, P.; Gil, S. Tetrahedron: Asymmetry 2005, 16, 2673–2679.         [ Links ]

9. Jung, Y. E., Song, B. M., Chang, S.–K. J. Chem. Soc. Perkin Trans. 2 1995, 2031–2034.         [ Links ]

10. Voyer, N.; Deschénes, D.; Bernier, J.; Roby, J. J. Chem. Soc., Chem. Commun. 1992, 134–136.         [ Links ]

11. Hernández, J. V.; Oliva, A. I.; Simón, L.; Muñiz, F. M.; Grande, M.; Morán, J. R. Tetrahedron Lett. 2004, 45, 4831–4833.         [ Links ]

12. Tsubaki, K., Tanaka, H., Furuta, T., Tanaka, K., Kinoshita, T., Fuji, K. Tetrahedron 2002, 58, 5611–5617.         [ Links ]

13. Galán, A.; Andreu, D.; Echavarren, A. M.; Prados, P.; De Mendoza, J. J. Am. Chem. Soc. 1992, 114, 1511–1512.         [ Links ]

14. Reetz, M. T.; Huff, J.; Rudolph, J.; Töllner, K.; Deege, A.; Goddard, R. J. Am. Chem. Soc. 1994, 116, 11588–11589.         [ Links ]

15. Barboiu, M. D.; Hovnanian, N. D.; Luca, C.; Cot, L. Tetrahedron 1999, 55, 9221–9232.         [ Links ]

16. Demirel, N.; Bulut, Y.; Hosgoren, H. Tetrahedron: Asymmetry 2004, 15, 2045–2049.         [ Links ]

17. Breccia, P.; Van Gool, M.; Pérez–Fernández, R.; Martín–Santamaría, S.; Gago, F.; Padros, P.; De Mendoza, J. J. Am. Chem. Soc. 2003, 125, 8270–8284.         [ Links ]

18. Hansson, A. P.; Norrby, P.–O.; Warnmark, K. Tetrahedron Lett. 1988, 39, 4565–4568.         [ Links ]

19. Kryatova, O. P., Kolchinski, A. G., Rybak–Akimova, E. V. Tetrahedron 2003, 231–239.         [ Links ]

20. Izatt, R. M.; Lamb, J. D.; Izatt, N. E.; Rossiter, B. E. Jr., Christensen, J. J., Haymore. B. L. J. Am. Chem. Soc. 1979, 101, 6273–6276.         [ Links ]

21. Buschmann, H.–J.; Schollmeyer, E.; Mutihac, L. J. Inclusion Phenom. Macrocyclic Chem. 2001, 40, 199–202.         [ Links ]

22. (a) Defen, W.; Xiaoqiang, S.; Dengjin, W.; Hongwen, H. Youji Huaxue 1987, 3, 219–223.         [ Links ] (b) Xiaochun, Ch.; Defen, W.; Denjing, W.; Hongwen, H. Chem. Res. Chin. Univ. 1991, 7, 255–260.         [ Links ] (c) Dengjin, W.; Defen, W.; Xiaoqiang, S.; Hongwen, H. Gaodeng Xuexiao Huaxue Xuebao 1990, 11(7), 672–675.         [ Links ] (d) Defen, W.; Denjing, W.; Hongwen, H. Gaodeng Xuexiao Huaxue Xuebao 1990, 11(3), 276–270.         [ Links ]

23. Jaffe, H.H.; Orchin, M. Theory and Applications of Ultraviolet Spectroscopy. John Wiley & Sons, USA, 1962, p. 186.         [ Links ]

24. Connors, K. A. Binding Constants. The Measurement of Molecular Complex Stability. John Wiley & Sons, USA, 1987, p. 24.         [ Links ]

25. Schneider, H.–J.; Yatsimirsky, A. K.: Principles and Methods in Supramolecular Chemistry. John Wiley & Sons, England, 2000, p.142.         [ Links ]

26. Marquis, D.; Desvergne, J.–P.; Bouas–Laurent, H. J. Org. Chem. 1995, 60, 7984–7996.         [ Links ]

27. Gaviña, F.; Luis, S.V.; Costero, A.M.; Burgete, M.I.; Rebek, J. J. Am. Chem. Soc. 1988, 110, 7140–7143.         [ Links ]

28. Al–Jallal, N. A.; Al–Kahtani, A. A.; El–Azhary, A. A. J. Phys. Chem. A, 2005, 109(16), 3694–3703.         [ Links ]

29. Buschmann, H. –J.; Mutihac, L.; Jansen, K. J. Inclusion Phenom. Macrocyclic Chem. 2001, 39, 1–11.         [ Links ]

30. Zhu, L.–N.; Gao, S.; Huo, L.–H. Acta Cryst. E63 2007, o4924.         [ Links ]

31. Lehn, J. M., Supramolecular Chemistry VCH, Germany, 1995, p. 26–28.         [ Links ]

32. Ramírez, J. Z.; Vargas, R.; Garza, J. J. Mex. Chem. Soc. 2008, 52, 31–35.         [ Links ]

33. Guo, H.; Sirois, S.; Proynov, E. I.; Salahub, D. R. Density Functional Theory and its Applications to Hydrogen–bonded Systems. Theoretical Treatments of Hydrogen bonding; Hadzi, D., Ed.; John Wiley & Sons Ltd: Chichister, UK, 1997.         [ Links ]

34. Vogel, A. I.; Tatchell, A. R.; Furnis, B. S.; Hannaford, A. J.; Smith, P.W.G. Vogel's Textbook of Practical Organic Chemistry.5th Edition. Prentice Hall, 1989.         [ Links ]

35. Shishkina, S. V.; Shishkin, O. V.; Grygorash R. Y.; Mazepa, A. V.; Rakipov, I. M.; Yakshin, V. V.; Kotlyar, S. A.; Kamalov, G. L. J. Molecular Struct. 2007, 832 199–208        [ Links ]

36. Gaussian 03, Revision D.01, M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery, Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al–Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, C. Gonzalez, and J. A. Pople, Gaussian, Inc., Wallingford CT, 2004.         [ Links ]

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons