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Organic halide-alcohol interactions: Observation by means of the glass transition

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Abstract

The glass-transition temperature (T g) in binary mixtures of the primary alkanols with CBr 4 and CHBr 3 has been measured as a function of composition. The results are compared with earlier studies on alkanol solutions of organic chlorides. The initial molar slope (IMS) of theT g vs. composition curve at the pure alkanol indicates formation of a 1:1 halide-alkanol complex stabilized by a specific halogen-oxygen interaction. The IMS values decrease in the order CBr 4 >CHBr 3 >CCl 4 >CHCl 3 >CH 2 Cl 2 , reflecting decreasing stability of the complex.

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References

  1. A. V. Lesikar,J. Chem. Phys. 63, 2297 (1975).

    Google Scholar 

  2. A. V. Lesikar,J. Chem. Phys. 64, 3086 (1976).

    Google Scholar 

  3. A. V. Lesikar,J. Chem. Phys. 66, 4273 (1977).

    Google Scholar 

  4. A. V. Lesikar,J. Solution Chem. 6, 81 (1977).

    Google Scholar 

  5. G. Scatchard and C. L. Raymond,J. Am. Chem. Soc. 60, 1278 (1938).

    Google Scholar 

  6. I. Brown, W. Fock, and F. Smith,J. Chem. Thermodyn. 1, 273 (1969).

    Google Scholar 

  7. A. V. Lesikar,J. Phys. Chem. 80, 1005 (1976).

    Google Scholar 

  8. B. Wunderlich,J. Phys. Chem. 64, 1052 (1960).

    Google Scholar 

  9. A. J. Easteal, E. J. Sare, C. T. Moynihan, and C. A. Angell,J. Solution Chem. 3, 807 (1974).

    Google Scholar 

  10. J. H. Gibbs and E. A. DiMarzio,J. Chem. Phys. 28, 373 (1958).

    Google Scholar 

  11. E. A. DiMarzio and J. H. Gibbs,J. Polym. Sci. 1A, 1417 (1963).

    Google Scholar 

  12. A. V. Lesikar, unpublished data.

  13. J. H. Hildebrand and R. L. Scott,The Solubility of Nonelectrolytes, 3rd ed. (Dover Publications, Inc., New York, 1964), Chap. VII.

    Google Scholar 

  14. M. D. Joesten and L. J. Schaad,Hydrogen Bonding (Marcel Dekker, Inc., New York, 1974).

    Google Scholar 

  15. J. P. Sheridan, D. E. Martire, and Y. B. Tewari,J. Am. Chem. Soc. 94, 3294 (1972).

    Google Scholar 

  16. D. E. Martire, J. P. Sheridan, J. W. King, and S. E. O'Donnell,J. Am. Chem. Soc. 98, 3101 (1976).

    Google Scholar 

  17. G. M. Janini, J. W. King, and D. E. Martire,J. Am. Chem. Soc. 96, 5368 (1974).

    Google Scholar 

  18. D. E. Martire,Anal. Chem. 46, 1712 (1974).

    Google Scholar 

  19. G. C. Pimentel and A. L. McClellan,The Hydrogen Bond (W. H. Freeman Co., San Francisco, 1960), pp. 348 and 349.

    Google Scholar 

  20. E. M. Arnett,Prog. Phys. Org. Chem. 1, 223 (1963).

    Google Scholar 

  21. J. A. Riddick and W. B. Bunger,Organic Solvents, 3rd ed. (Wiley-Interscience, New York, 1970).

    Google Scholar 

  22. W. B. Person,J. Am. Chem. Soc. 87, 167 (1965).

    Google Scholar 

  23. M. W. Hanna,J. Am. Chem. Soc. 90, 285 (1968).

    Google Scholar 

  24. J. L. Lippert, M. W. Hanna, and P. J. Trotter,J. Am. Chem. Soc. 91, 4035 (1969).

    Google Scholar 

  25. J. H. Hildebrand, J. M. Prausnitz, and R. L. Scott,Regular and Related Solutions (Van Nostrand Reinhold Co., New York, 1970), p. 62; J. H. Hildebrand and R. L. Scott,The Solubility of Nonelectrolytes, 3rd ed. (Dover Publications, Inc., New York, 1964), Chap. IV.

    Google Scholar 

  26. E. A. DiMarzio,J. Res. Nat. Bur. Stand. Sect. A 68, 611 (1964).

    Google Scholar 

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Lesikar, A.V. Organic halide-alcohol interactions: Observation by means of the glass transition. J Solution Chem 6, 839–853 (1977). https://doi.org/10.1007/BF00648073

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