HYDROLYTIC STABILITY OF IMIDES OF DIFFERENT STRUCTURES

Authors

  • A. I. Donskikh
  • G. M. Tseitlin
  • O. I. Tomina
  • Z. F. Saikina
  • Ju. E. Doroshenko

Abstract

The conversion kinetics of N(o-carboxyphenyl)naphthalimide has been studied in buffer solutions over a pH range 5-12.6 and temperature range 25-70 °C. The naphthalimide hydrolysis is shown to be a reversible reaction. The mechanism of the alkaline hydrolysis of N(o- carboxyphenyl) phthalimide is proposed. The structure dependence of the imide hydrolytic stability is explained on the basis of the suggested mechanism.

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How to Cite

Donskikh, A. I., Tseitlin, G. M., Tomina, O. I., Saikina, Z. F., Doroshenko, J. E. “HYDROLYTIC STABILITY OF IMIDES OF DIFFERENT STRUCTURES ”, Periodica Polytechnica Chemical Engineering, 33(1), pp. 61–67, 1989.

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Articles