Metal complexes with alizarin and alizarin red S: Electronic absorption spectra and structure of ligands

Most of the πl,π* bands of metal alizarinates are shown to be due to the 2,9- or 1,2-anthraquinoid structures. Bimetallic alizarinates with the 9,10-anthraquinoid structure are not formed because of the adjacent negatively charged oxygen atoms. The long-standing dispute concerning the structure of red metal alizarinates is solved: complexation always occurs at the peri- or ortho-hydroxycarbonyl group and involves the tautomeric anthraquinoid forms.

Authors
Number of issue
5
Language
English
Pages
365-370
Status
Published
Volume
30
Year
2004
Organizations
  • 1 Russ. Univ. of Peoples' Friendship, ul. Miklukho-Maklaya 6, Moscow, 117198, Russian Federation
Keywords
alizarin; alizarin red s; anthraquinone derivative; carbonyl derivative; hydroxyl group; ligand; metal; oxygen; absorption; article; atom; chemical structure; complex formation; electronics; quantum chemistry; synthesis
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/3640/
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Soldatenkov A.T., Temesgen A.V., Kolyadina N.M.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 40. 2004. P. 537-560