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Enthalpies of dilution of aqueous systems containing hexamethylenetetramine and other nonelectrolytes

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Abstract

Enthalpies of dilution of aqueous systems containing hexamethylenetetramine, alone and in ternary system with each of mannitol, myoinositol, cyclohexanol, formamide, dimethylformamide, and trioxane have been determined. The data have been treated in terms of the Savage-Wood additivity principle and first estimates for the pairwise groups interaction enthalpies of N/N, CH2/N, CHOH/N, COHN/N and −O−/N have been made. The results are discussed in light of all other known group interaction enthalpies. The limitations and utilities of the Savage-Wood principle are reviewed.

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References

  1. I. R. Tasker and R. H. Wood,J. Phys. Chem. 86, 4040 (1982).

    Google Scholar 

  2. I. R. Tasker and R. H. Wood,J. Solution Chem. 11, 295 (1982).

    Google Scholar 

  3. I. R. Tasker and R. H. Wood,J. Solution Chem. 11, 469 (1982).

    Google Scholar 

  4. I. R. Tasker and R. H. Wood,J. Solution Chem. 11, 481 (1982).

    Google Scholar 

  5. J. J. Savage and R. H. Wood,J. Solution Chem. 5, 733 (1976).

    Google Scholar 

  6. See cross-references in Refs. 1–4.

  7. I. R. Tasker, R. H. Wood, and J. H. Albert, to be published.

  8. G. Barone, V. Crescenzi, A. M. Liquori, and F. Quadrifoglio,J. Phys. Chem. 71, 984 (1967).

    Google Scholar 

  9. V. Crescenzi, F. Quadrifoglio, and V. Vitagliano,J. Phys. Chem. 71, 2313, 1967.

    Google Scholar 

  10. L. Constantino, V. Crescenzi, and V. Vitagliano,J. Phys. Chem. 72, 149, 1968.

    Google Scholar 

  11. G. Barone, V. Crescenzi, and V. Vitagliano,J. Phys. Chem. 72, 2588, 1968.

    Google Scholar 

  12. F. Quadrifoglio, V. Crescenzi, A. Cesaro, and F. Delben,J. Phys. Chem. 75, 3633, 1971.

    Google Scholar 

  13. G. Barone, P. Bonpresa, P. Cacace, G. Castronuovo, V. Elia, and N. F. Fragassi, paper presented at Journees de Calorimetrie D'Analyse Thermique, Torino (Italy), June 1978.

  14. J. L. Neal and D. A. I. Goring,J. Phys. Chem. 74, 658 (1970).

    Google Scholar 

  15. T. C. W. Mak,J. Phys. Chem. 43, 2799 (1965).

    Google Scholar 

  16. G. Barone, G. Castronuovo, A. Cesaro, and V. Elia,J. Solution Chem. 9, 867 (1980).

    Google Scholar 

  17. F. Franks, M. Pedley, and D. S. Reid,J.C.S. Faraday Trans. I 72, 184 (1976).

    Google Scholar 

  18. J. E. Desnoyers, G. Perron, and L. Avedikian, J.-P. Morel,J. Solution Chem. 5, 631 (1976).

    Google Scholar 

  19. H. L. Friedman and C. V. Krishan,J. Solution Chem. 2, 119 (1973).

    Google Scholar 

  20. G. Barone, P. Cacace, G. Castronuovo, and V. Elia,J.C.S. Faraday Trans. I 77, 1569 (1981).

    Google Scholar 

  21. R. H. Wood and L. H. Hiltzik,J. Solution Chem. 9, 45 (1980).

    Google Scholar 

  22. F. Franks and M. D. Pedley,J.C.S. Faraday Trans. I 77, 1341 (1981).

    Google Scholar 

  23. J. V. Coe, Honors Thesis 1979, Swarthmore College, Swarthmore, PA.

  24. B. Y. Okamoto, R. H. Wood, J. E. Desnoyers, G. Perron, and L. Delorme,J. Solution Chem. 10, 139 (1981).

    Google Scholar 

  25. R. W. Gurney,Ionic Processes in Solution (Dover, New York, 1953).

    Google Scholar 

  26. R. Cambier and A. Brochet,Bull. Soc. Chim. France 13, 392 (1895).

    Google Scholar 

  27. M. Delepine,Bull. Soc. Chim. France 13, 352 (1895).

    Google Scholar 

  28. W. J. M. Heuvelsland, C. de Visser and G. Somsen,J.C.S. Faraday Trans. I 77, 191 (1981).

    Google Scholar 

  29. G. Barone, P. Cacace, G. Castronuovo, and V. Elia,Gazz. Chim. It. 110, 215 (1980).

    Google Scholar 

  30. G. Barone, P. Cacace, G. Castronuovo, and V. Elia,Canad. J. Chem. 59, 1257 (1981).

    Google Scholar 

  31. A. L. Harris, P. T. Thompson, and R. H. WoodJ. Solution Chem. 9, 305 (1980).

    Google Scholar 

  32. W. Ramsden,J. Physiol. 28, XXII (1902).

    Google Scholar 

  33. C. Tanford,Adv. Prot. Chem. 24, 1 (1970).

    Google Scholar 

  34. J. Leonis,Arch. Biochem. Biophys. 65, 182 (1956).

    Google Scholar 

  35. C. E. Buckley, P. L. Whitney, and C. Tanford,Proc. Nat. Acad. Sci. 50, 827. (1963).

    Google Scholar 

  36. T. Tagaki and T. Isomeura,Biochem. Biophys. Acta 130, 233 (1966).

    Google Scholar 

  37. K. Kawara, A. G. Kirschner, and C. Tanford,Biochemistry 4, 1203 (1965).

    Google Scholar 

  38. A. E. Russel and D. R. Cooper,Biochem. J. 113 221 (1969).

    Google Scholar 

  39. F. G. Hopkins,Nature 126, 383 (1930).

    Google Scholar 

  40. M. A. Lauffer,J. Phys. Chem. 65, 1793 (1943).

    Google Scholar 

  41. M. L. Anson and A. E. Mirsky,J. Gen. Physiol. 17, 399 (1933–1934).

    Google Scholar 

  42. L. Pauling and A. E. Mirsky,Proc. Nat. Acad. Sci. 22, 439 (1936).

    Google Scholar 

  43. J. K. Frensdorff, M. T. Watson, and W. Kauzmann,J. Am. Chem. Sci. 75, 5154 (1953).

    Google Scholar 

  44. R. B. Simpson and W. Kauzmann,J. Am. Chem. Soc. 75, 5139 (1953).

    Google Scholar 

  45. I. R. Tasker, Ph.D. Thesis, Sheffield, U. K., 1979.

  46. J. F. Brandts, inStructure and Stability of Biological Macromolecules S. N. Timsheff, G. D. Fasman Eds., (Marcel Dekker, New York, 1969).

    Google Scholar 

  47. W. P. Jencks,Fed. Proc. 24, 50 (1965).

    Google Scholar 

  48. D. R. Robinson and W. P. Jencks,J. Biol. Chem. 238, 1558 (1963).

    Google Scholar 

  49. N. C. Pace and C. Tanford,Biochemistry 7, 198 (1968).

    Google Scholar 

  50. J. Skerjanc and S. Lapanje,Croatica Chem. Acta. 41, 111 (1969).

    Google Scholar 

  51. J. A. Gordon and J. R. Warren,J. Biol. Chem. 243, 5663 (1968).

    Google Scholar 

  52. J. R. Warren and J. A. Gordon,J. Biol. Chem. 245, 4097 (1970).

    Google Scholar 

  53. J. R. Warren and J. A. Gordon,Biochim. Biophys. Acta. 229, 216 (1971).

    Google Scholar 

  54. J. Span and S. Lapanje,Biochim. Biophys. Acta. 295, 371 (1973).

    Google Scholar 

  55. C. de Visser, W. J. M. Heuvelsland, and G. Somsen,J. Solution Chem. 7, 193 (1978).

    Google Scholar 

  56. W. J. M. Heuvelsland, C. de Visser and G. Somsen,J.C.S. Faraday Trans. I 77, 1191 (1981).

    Google Scholar 

  57. G. M. Blackburn, T. H. Lilley, and L. Walmsley,J.C.S. Chem. Comm. 1091 (1980);J.C.S. Faraday Trans. I 78, 1641 (1978).

  58. G. M. Blackburn, T. H. Lilley, and L. Walmsley,J.C.S. Faraday Trans I 76, 915 (1980).

    Google Scholar 

  59. T. H. Lilley, private communication, 1981.

  60. B. Y. Okamoto, R. H. Wood, and P. T. Thompson,J.C.S. Faraday Trans. I 74, 1990 (1978).

    Google Scholar 

  61. R. H. Wood and J. E. Desnoyers; in preparation.

  62. L. R. Pratt and D. Chandler,J. Solution Chem. 9, 1 (1980);J. Chem. Phys. 73, 3434 (1980).

    Google Scholar 

  63. G. Barone, P. Cacace, G. Castronuovo, and V. Elia,Carbohydrate Research 91, 101 (1981).

    Google Scholar 

  64. G. Barone, P. Cacace, G. Castronuovo, and V. Elia,Carbohydrate Research 93, 11 (1981).

    Google Scholar 

  65. G. Barone, B. Bove, G. Castronuovo, and V. Elia,J. Solution Chem. 10, 803 (1981).

    Google Scholar 

  66. G. Barone, G. Castronuovo, and V. Elia,Adv. Mole. Relax. Inter. Processes, in press, 1982.

  67. G. Barone, G. Castronuovo, D. Doucas, V. Elia, and A. Mattia. Submitted for publication, 1982.

  68. G. Barone, V. Elia, and E. Rizzo,J. Solution Chem. 11, 687 (1982).

    Google Scholar 

  69. G. Barone, P. Cacace, and G. Castronuovo, V. Elia. Submitted for publication, 1982.

  70. G. Barone. Private communication, 1982.

  71. G. Barone, P. Cacace, G. Castronuovo, and V. Elia,Gaz. Chim. Ital. 112, (1982).

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Tasker, I.R., Wood, R.H. Enthalpies of dilution of aqueous systems containing hexamethylenetetramine and other nonelectrolytes. J Solution Chem 11, 729–747 (1982). https://doi.org/10.1007/BF00645339

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