Cationic Complexes of Magnesium with Phenanthroline. Synthesis, Structural Features and Antibacterial Activity
- Autores: Potylitsyna S.M.1,2, Koshenskova K.A.1, Nikiforova M.E.1, Razvorotneva L.S.1,3, Dolgushin F.M.1, Bekker O.B.4, Zaeva A.S.5, Kiskin M.A.1, Eremenko I.L.1,6, Lutsenko I.A.1
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Afiliações:
- Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
- Lomonosov Moscow State University
- National Research University Higher School of Economics
- Vavilov Institute of General Genetics, Russian Academy of Sciences
- Amur State Medical Academy of the Ministry of Healthcare of the Russian Federation
- Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- Edição: Volume 51, Nº 6 (2025)
- Páginas: 366-376
- Seção: Articles
- URL: https://rjdentistry.com/0132-344X/article/view/687246
- DOI: https://doi.org/10.31857/S0132344X25060028
- EDN: https://elibrary.ru/KIGQGL
- ID: 687246
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Resumo
The interaction of magnesium oxide/magnesium pivalate with aromatic heterocyclic acids (3-indolecarboxylic (Hind); 2-thiophenecarboxylic (Htph)) and 1,10-phenanthroline (phen) led to the formation of cationic complexes [Mg(phen)(ind)(H2O)3]+ind−·2phen·1.5H2O (I) and [Mg(phen)(H2O)4]32+·6thp−·2phen (II), the structure of which was established by direct X-ray diffraction analysis (CCDC Nos. 2422043 (I) and 2422042 (II)). According to X-ray data, the complexing agent in compounds I and II is in a distorted octahedral environment {MgN2O4} with the coordination number of the magnesium atom equal to 6. In the crystal packing of I, stacking interactions are observed between the aromatic phen cycles, forming parallel stacks held together by hydrogen bonds. Outer-sphere tph− in II form strong hydrogen bonds with the coordinated water molecules, forming an 1D hydrogen-bonded framework. Antibacterial activity against a non-pathogenic strain of M. smegmatis and two strains — Lactobacterium brevis and Lactobacillus fermentum was determined for I and II. Antiproliferative activity of I was determined against cancer lines of human ovarian adenocarcinoma (SKOV3), breast adenocarcinoma (MCF7) and glioblastoma (A172).
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Sobre autores
S. Potylitsyna
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences; Lomonosov Moscow State University
Email: irinalu05@rambler.ru
Rússia, Moscow; Moscow
K. Koshenskova
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: irinalu05@rambler.ru
Rússia, Moscow
M. Nikiforova
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: irinalu05@rambler.ru
Rússia, Moscow
L. Razvorotneva
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences; National Research University Higher School of Economics
Email: irinalu05@rambler.ru
Rússia, Moscow; Moscow
F. Dolgushin
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: irinalu05@rambler.ru
Rússia, Moscow
O. Bekker
Vavilov Institute of General Genetics, Russian Academy of Sciences
Email: irinalu05@rambler.ru
Rússia, Moscow
A. Zaeva
Amur State Medical Academy of the Ministry of Healthcare of the Russian Federation
Email: irinalu05@rambler.ru
Rússia, Blagoveschensk
M. Kiskin
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: irinalu05@rambler.ru
Rússia, Moscow
I. Eremenko
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences; Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: irinalu05@rambler.ru
Rússia, Moscow; Moscow
I. Lutsenko
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Autor responsável pela correspondência
Email: irinalu05@rambler.ru
Rússia, Moscow
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