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Carbon and chlorine kinetic isotope effects and pseudo-first order rate constants were measured for the hydrolysis of ethyl, benzyl, and isopropyl chloroformate in various mixtures of the binary solvent water-1,4-dioxane. Rate constants decreased as the percentage of 1,4-dioxane increased for all three chloroformates. Carbon-13 kinetic isotope effects (k12/k13) for hydrolysis of these compounds were 1.039-1.042 for ethyl chloroformate (0-75% 1,4-dioxane), 1.034-1.039 for benzyl chloroformate (15-75% 1,4-dioxane), and 1.025-1.037 for isopropyl chloroformate (25-75% 1,4-dioxane). Chlorine-37 kinetic isotope effects (k35/k37) were measured for benzyl and isopropyl chloroformates in 25% 1,4-dioxane (1.0088, benzyl; 1.0080 isopropyl) and 75% 1,4-dioxane (1.0090, benzyl; 1.0102 isopropyl). These data are consistent with an associative mechanism for benzyl and ethyl chloroformates, but hydrolysis of isopropyl chloroformate appears to be dissociative in polar solvents.
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Tom
Strony
1721--1731
Opis fizyczny
Bibliogr. 18 poz., rys.
Twórcy
autor
- Department of Biochemistry, The Beadle Center, University of Nebraska-Lincoln, Lincoln, NE 68588-0664, USA
autor
- Department of Chemistry (1-19), Technical University of Łódź, Żeromskiego 116, 90-924 Łódź, Poland
autor
- Department of Chemistry (1-19), Technical University of Łódź, Żeromskiego 116, 90-924 Łódź, Poland
autor
- Department of Biochemistry, The Beadle Center, University of Nebraska-Lincoln, Lincoln, NE 68588-0664, USA
Bibliografia
- 1. Jia Z.S., Rudzinski J., Paneth P. and Thibblin A., J. Org. Chem., 67, 177 (2002).
- 2. (a) Kevill D.N., In The chemistry of acyl halides, Patai S.,Ed. 1972, Interscience Publishers, NY p. 381; (b) Kivinen A„ The chemistry ofacyl halides, Patai S., Ed. 1972, Interscience Publishers, NY p. 177 ; (c) Kevill D.N. and D’Souza M.J., J. Org. Chem., 63,2120 (1998).
- 3. (a) Archer B.L. and Hudson R.F., J. Chem. Soc., 3259 (1950); (b) Brown D. A. and Hudson RF J Chem Soc., 3352(1953).
- 4. Song B.D. and Jencks W.P., J. Am. Chem. Soc., Ill, 8470 (1989),
- 5. (a) Hall H.K., J. Am. Chem. Soc., 77,5993 (1955); (b) Kivinen A., Acta Chem. Scand., 19,845 (1965V (c) Queen A., Can. J. Chem., 45,1619 (1967).
- 6. Crunden E.W. and Hudson R.F., J Chem. Soc., 3748 (1961).
- 7. (a)Kevill D.N. andD ’Souza M .J., J. Chem. Soc.PerkinsII, 2,17(1997); (b)Kevill D.N. andD’Souza M. J. J. Org. Chem., 62, 7869 (1997).
- 8. Reichardt C., Solvents and solvent effects in organic chemistry, VCH Publishers, NY 1988.
- 9. While we recognize that associative (tetrahedral intermediate) and concerted (tetrahedral transition state with no intermediate) mechanisms are distinct from each other, we have chosen to use the term “associative" as including the possibility of both associative or concerted mechanisms in order to simplify the wording of the discussion. Our data alone cannot distinguish between the two possibilities.
- 10. Hudson R.F. and Green M., J. Chem. Soc., 1055 (1962).
- 11. Butler A.R., Robertson I.H. and Bacaloglu R., J. Chem. Soc. Perkins II, 1733 (1974),
- 12. Shiner V.J, and Wilgis F.P., In Isotopes in Organic Chemistry, Vol. 8, Buncel E., Saunders W.H.J., Eds., Elsevier, Amsterdam, 1992, p. 239.
- 13. O’Leary MH. and Marlier J.F., J. Am. Chem. Soc., 101, 3300 (1979).
- 14. Marlier J.F., J. Am. Chem. Soc., 115, 5953 (1993).
- 15. Kevill D.N., Kyong, J.B. and Weitl F.L., J. Org. Chem., 55, 4304 (1990).
- 16. Melander L. and Saunders W.H., Reactions rates of isotopic molecules, J. Wiley & Sons, NY 1980.
- 17. O’Leary M.H., In Methods in Enzymology, Vol. 64, Academic Press, NY 1981, p. 83,
- 18. Westaway K.C., Koerner T., Fang Y.-R, Rudzinski J. and Paneth P., Anal. Chem,, 70, 3548 (1998).
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Bibliografia
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bwmeta1.element.baztech-article-BUJ1-0021-0035