Colloid and Polymer Science

, Volume 274, Issue 1, pp 59–69 | Cite as

On the determination of polarity parameters of silica by means of solvatochromic probe dyes

  • S. Spange
  • A. Reuter
  • E. Vilsmeier
Original Contribution

Abstract

Empirical “solvent” parameters of silica surfaces are determined by means of solvatochromic dyes, e.g., Cu(tmen) (acac)+ ClO 4 /B(C6H5) 4 , Fe(phen)2(CN)2, and Michlers Ketone dissolved in 1,2-dichloroethane or cyclohexane. The values obtained by UV/VIS-measurements are compared with both the polarity scales of Kamlet and Taft and with Gutmann's donor and acceptor numbers. Kamlet and Taft's α-parameter (the hydrogen-bond donation capacity of a solvent) is determined independently by means of salicylideneaniline. The π* of silica is determined using 5-N,N-dimethylamino-5′-nitro-2,2′-bithiophene and the complex of tetracyanoethylene with Michlers Ketone, respectively. Further on the reliabilities of the obtained Kamlet-Taft parameters α, β, and π* are checked by comparism with experimental and calculated values of theET(30)-parameter of silica by means of multi-parameter regression analysis. The surface properties of silica are influenced mainly by HBD-properties α (75%) and dipolarity/polarizability π* (20%), but hardly by the HBA-properties β (<5%). UV/VIS-measurements were carried out in a special equipment with glass fiber optics, A drawing of the apparatus is given.

Key words

Acidity basicity dipolarity silica polarity solvatochromic dyes acceptor numbers donor numbers 

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References

  1. 1.
    Spange S, Walther R, Schmiede B (1992) GIT-Zeitschrift für das Laboratorium 92:736–737Google Scholar
  2. 2.
    Tenabe K, Hattori H, Yamaguchi T, Tanaka T (1989) Acid-Base-Catalysis VCH Publishers, New YorkGoogle Scholar
  3. 3.
    Arnett EM, Cassidy KF (1988) Rev Chem Intermed 2:27–64Google Scholar
  4. 4.
    Chronister CW, Drago RS (1993) J Am Chem Soc 115:4793–4798Google Scholar
  5. 5.
    Kriegsmann H (1988) Z Phys Chem Leipzig 269:1030–1036Google Scholar
  6. 6.
    Lindley SM, Flowers GC, Leffler JE (1985) J Org Chem 50:607–610Google Scholar
  7. 7.a)
    Spange S, Keutel D, Simon F (1992) J Chim Phys 89:1615–1622Google Scholar
  8. 7.b)
    Spange S, Keutel D (1992) Liebigs Ann Chem 423–428Google Scholar
  9. 7.c)
    Spange S, Hortschansky P, Ulbricht A, Heublein G (1987) Z Chem 27:207–208Google Scholar
  10. 8.a)
    Reichardt C (1994) Chem Rev 94: 2319–2358Google Scholar
  11. 8.b)
    Reichardt C (ed 1988) “Solvents and Solvent effects in organic chemistry” 2nd ed VCH Publishers Weinheim and references thereinGoogle Scholar
  12. 9.
    Gutmann V (1976) Coord Chem Rev 18:225–255Google Scholar
  13. 10.a)
    Kamlet MK, Abboud JL, Abraham MH, Taft RW (1983) J Org Chem 48: 2877–2887.Google Scholar
  14. 10.b)
    Kamlet MJ, Jones ME, Taft RW, Abboud J-L (1979) J Chem Soc Perkin Trans II:342–348Google Scholar
  15. 11.
    Laurence C, Berthelot M, Lucon M, Morris DG (1994) J Chem Soc Perkin Trans II:491–493Google Scholar
  16. 12.a)
    Maria PC, Gal FJ, Exner O (1994) “The site of protonation of 4-nitroaniline and of similar aromatic derivatives”, 6th CAIC-conference prague 1994, poster representationGoogle Scholar
  17. 12.b)
    Maria PC (1994) unpublished results communicated to the authors.Google Scholar
  18. 12.c)
    Taft RW, Topson RD (1987) Prog Phys Org Chem 16:1Google Scholar
  19. 13.
    Schneider H, Migron Y, Marcus Y (1992) Zeitschrift Phys Chem NF 175:145–164Google Scholar
  20. 14.
    Spange S, Simon F, Heublein G, Jacobasch HJ, Börner M (1991) Coll & Polym Sci 269:173–178Google Scholar
  21. 15.
    Soukup RW, Schmid W (1985) J Chem Educ 62:459–462Google Scholar
  22. 16.
    Soukup RW, Sone K (1987) Bull Chem Soc Jpn 60:2286–2288Google Scholar
  23. 17.
    Migron Y, Marcus Y (1991) J Phys Org Chem 4:310–314Google Scholar
  24. 18.
    Spange S, Fandrei D, Simon F, Jacobasch HJ (1994) Coll & Polym Sci 272:99–107Google Scholar
  25. 19.
    Czapkiewicz J, Czapkiewicz-Tutaj B (1980) J Chem Soc Faraday Trans I 76: 1663–1668Google Scholar
  26. 20.
    Davis KMC (1967) J Chem Soc 1128–1130Google Scholar
  27. 21.
    Spange S, Vilsmeier E, unpublished resultsGoogle Scholar
  28. 22.
    Farkas J, Hampden-Smith MJ, Kodas TT (1994) J Phys Chem 98:6753–6762Google Scholar
  29. 23.
    Arnett EM, Ahsan T (1991) J Am Chem Soc 113:6861–6864Google Scholar
  30. 24.
    Dutta PK, Turbeville W (1991) J Phys Chem 95:4087–4092Google Scholar
  31. 25.
    Handreck GP, Smith TD (1988) J Chem Soc Faraday Trans I 84:1847–1852Google Scholar
  32. 26.
    Effenberger F, Würthner F (1993) Angew Chem 105:742–744Google Scholar
  33. 27.
    Marcus Y (1991) J Sol Chem 20:929–944Google Scholar
  34. 28.
    Spange S, Lauterbach M, Gyra AK, Reichardt C (1991) Liebigs Ann Chem 223–229Google Scholar
  35. 29.
    Spange S, Reuter A, Schramm A, Reichardt C (1995) Organic Reactivity (Tartu) 29:91–92Google Scholar
  36. 30.
    Park JH, Carr PW (1989) J Chromatographie 465:137–156Google Scholar

Copyright information

© Steinkopff Verlag 1996

Authors and Affiliations

  • S. Spange
    • 1
  • A. Reuter
    • 1
  • E. Vilsmeier
    • 1
  1. 1.Lehrstuhl für PolymerchemieTU Chemnitz/ZwickauChemnitz

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