Termodesorption mass-spectrometric investigation of isomeric derivatives of N-azoilmethylbenzoic asides

  • Zoya P. Belousova the senior lecturer, candidate of chemical sciences (postdoctoral studies and research), Chair of organic, bioorganic and medical chemistry, Samara State University, Samara
  • Pyotr P. Purygin head of chair, the professor, doctor of chemical sciences (Doctor Of Science), Chair of the organic, bioorganic and medical chemistry, Samara State University, Samara
  • Vitaly A. Osyanin the senior teacher, candidate of chemical sciences (postdoctoral studies and research), Chair of organic chemistry, the Samara State University, Samara
  • Vera V. Varfolomeeva the senior lecturer, candidate of chemical sciences (postdoctoral studies and research), Chair of the ecology and life safety, Samara State Aerocosmic University by S.P.Korolev, Samara
  • Aleksey V. Uleanov candidate of chemical sciences, laboratory of phisical-chemical of base of chromatography and chromato-mass-spectrometry of A.N.Frumkin Institute of Phisical Chemistry and Electrochemistry RAS, Moscow
  • Aleksey K. Buryak head of laboratory, doctor of chemical sciences, laboratory of phisicalchemical of base of chromatography and chromatomass- spectrometry of A.N.Frumkin Institute of Phisical Chemistry and Electrochemistry RAS, Moscow, e-mail: akburyak@ipc.rssi.ru
Keywords: mass spectrometry, intramolecular hydrogen bond, derivatives of Nazolilmetilbenzojnyh of acids, isomers.

Abstract

In the present work correlations between a fragmentation under electron ionization and formation of
intramolecular hydrogen bond (IHB) are considered. Four pairsg of isomric molecules in which one isomer is
able to formation IHB and another – is not able are considered. As objects of research derivatives Nazolilmetilbenzojnyh
of acids are chosen that is connected with discovering of medical properties of many
molecules of the given class. By method of thermodesobtion mass spectrometry with electron ionization it is
shown that formation of IHB change a fragmentation. Stability of a molecular ion under electronic ionization
of orto- substituted isomers higher, than of meta- and/or para- substituted because of formation of
intramolecular hydrogen bond

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Published
2019-11-26
How to Cite
Belousova, Z. P., Purygin, P. P., Osyanin, V. A., Varfolomeeva, V. V., Uleanov, A. V., & Buryak, A. K. (2019). Termodesorption mass-spectrometric investigation of isomeric derivatives of N-azoilmethylbenzoic asides. Sorbtsionnye I Khromatograficheskie Protsessy, 11(3). Retrieved from https://journals.vsu.ru/sorpchrom/article/view/1931