Porphyrins. 29. Mass spectra of functionally substituted tetraarylporphyrin derivatives

Authors

  • И. М. Карнауx "Zashchita" Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow
  • А. C. Московкин "Zashchita" Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow
  • Г. B. Пономарев "Zashchita" Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow

Abstract

The mass spectral behavior of functionally substituted meso(p-adamantylphenyl)triphenylporphyrins and their p-methoxy-substituted analogs was studied. Breakdown of the M+ ions of these compounds proceeds chiefly with a loss of the functional substituent in the adamantane ring with the formation of ions, which make it possible to determine the nature of this substituent.

How to Cite
Karnaukh, I. M.; Moskovskin, A. S.; Ponomarev, G. V. Chem. Heterocycl. Compd. 1993, 29, 1418. [Khim. Geterotsikl. Soedin. 1993, 1642.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF00531403

Published

1993-12-25

Issue

Section

Original Papers