Physicochemical properties and structure of anthrapyrimidine and its derivatives

The method of electron spectroscopy entailing quantum-chemical calculations and the IR absorption spectra demonstrated the existence of the mono-, di-, and triprotonated forms of anthrapyrimidine and its derivatives in acidic solutions. The order of the protonation of the anthrapyrimidine molecule was established. It was shown that the two nitrogen atoms add protons; the third proton binds with the oxygen atom of the carbonyl group. In the molecule, the positive charge is localized within the pyrimidine ring. The energy characteristics of the anthrapyrimidine and its protonated forms were calculated. © 1991 Plenum Publishing Corporation.

Authors
Zaitsev B.E. 1 , Gromov D.N.1 , Ndongo Kh.A.1 , Odinets Z.K.1 , Sheban V.G.1 , Krasnova L.B. 1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
3
Language
English
Pages
321-324
Status
Published
Volume
27
Year
1991
Organizations
  • 1 P. Lumumba University of the Friendship of Peoples, Moscow, Russian Federation
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Varlamov A.V., Levov A.N., Fomichev A.A., Aliev A.E., Ustenko A.A., Pashentseva I.L., Prostatkov N.S., Dush Santush S.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 27. 1991. P. 173-177