Thermodynamics of amino acid methyl ester hydrochlorides - Crown ether complexes in methanol at 25°c

Journal of Solution Chemistry

Volumn 30, Issue 8, 2001, Pages 681-694

  Al Mustafa, Jamil ^a   Hamzah, Samer ^b   Marji, Deeb ^b  

^a JORDAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Jordan)

^b YARMOUK UNIVERSITY   (Jordan)

Author keywords

Amino acid methyl ester hydrochlorides; Compensation effect; Conductometric titration; Crown ethers; Methanol solutions

Indexed keywords

EID: 0035539519     PISSN: 00959782     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1011953211179     Document Type: Article

References (28)

1. 1. J. J. Christensen, D. J. Eatough, and R. M. Izatt, Chem. Rev. 74, 35 (1974).
2. 2. I. M. Kolthoff, Anal. Chem. 51, 1R (1979).
3. 3. C. J. Pederson, J. Amer. Chem. Soc. 89, 7017 (1967).
4. 4. C. J. Pederson, J. Amer. Chem. Soc. 92, 391 (1970).
5. 5. R. M. Izatt, K. J. Bradshaw, S. A. Nielsen, J. D. Lamb, and J. J. Christensen, Chem. Rev. 85, 271 (1985).
6. 6. R. M. Izatt, K. Pawlak, K. J. Bradshaw, and R. L. Bruening, Chem. Rev. 91, 1721 (1991).
7. 7. R. M. Izatt, K. J. Bradshaw, K. Pawlak, R. L. Bruening, and B. Tarbet, Chem. Rev. 92, 1261 (1992).
8. 8. D. Marji, K. Abbas, R. Saymeh, and Z. Taha, J. Incl. Phenom. 34, 49 (1991).
9. 9. J. M. Timko, R. C. Hegleson, M. Newcomb, G. W. Gokel, and D. J. Cram, J. Amer. Chem. Soc. 96, 7097 (1974).
10. 10. R. M. Izatt, X. Zhang, P. Huszthy, C. Y. Zhu, J. S. Hathaway, T. Wang, and Bradshaw, J. Incl. Phenom. 18, 49 (1991).
11. 11. M. Husani and Shamsipur, J. Incl. Phenom. 16, 479 (1980).
12. 12. H. J. Buschmann, E. Schollmeyer, and L. Mutihac, Supramol. Sci. 5, 139 (1998).
13. 13. G. A. Jeffrey, and W. Saenger, Hydrogen Bonding in Biological Structures (Springer, Berlin, 1994).
14. 14. J. M. Lehn, P. Vierling, Tetrahedron Lett. 21, 1323 (1980).
15. 15. E. Graph, J. P. Kintzinger, J. M. Lehn, and J. LeMoigne, J. Amer. Chem. Soc. 104, 1672 (1982).
16. 16. A. F. Danil de Namor, M. C. Ritt, D. F. Lewis, M. J. Schwing-Weill, and F. Arnaud-Neu, Pure Appl. Chem. 63, 1435 (1991).
17. 17. A. F. Danil de Namor, M. C. Ritt, M. J. Schwing-Weill, and F. Arnaud-Neu, D. F. Lewis, J. Chem. Soc. a Faraday Trans. 87, 3231 (1991).
18. 18. H. J. Buschman, E. Schollmeyer, and L. Mutihae, J. Incl. Phenom. 30, 21 (1998).
19. 19. M. Czekalla, K. Geo, B. Haberman, T. Kruger, H. Stephan, F. P. Schmidtchen, and R. Trultzsch, Poster PB 37, XXI International Symposium on Macrocyclic Chemistry, Montieatini Treme, Italy (1996).
20. 20. H. J. Buschmann, E. Schollmeyer, and L. Mutihac, Thermochim. Acta 316, 189 (1998).
21. 21. Y. Inoue and Hakushi, J. Chem. Soc. Perkin Trans. 2, 935 (1985).
22. 22. J. E. Lefter and E. Grunwald, Rates and Equilibria of Chemical Reactions (Wiley, New York, 1963), Chap. 9.
23. 23. H. S. Franks, J. Chem. Phys. 12, 478 (1945).
24. 24. R. Lumry and S. Rajender, Biopolymers, 9, 1125 (1970).
25. 25. E. Grunwald, Proc. 11th Intern. Conf. Chem. Thermodyn. Como, Italy (IUPAC, 1990).
26. 26. A. F. Danil de Namor, R. Traboulssi and D. F. Lewis, J. Amer. Chem. Soc. 112, 8442 (1990).
27. 27. Y. C. Wu and W. F. Koch, J. Solution Chem. 20, 391 (1991).
28. 28. K. Tawrah and S. Mizyed, J. Incl. Phenom. 6, 555 (1988).