from 01.01.2022 to 01.01.2024
Yaroslavl, Yaroslavl, Russian Federation
Yaroslavl, Yaroslavl, Russian Federation
UDC 546.654
UDC 547.831.7
The research examines the coordination of lanthanum(III) compound with 8 oxyquinoline. The article analyses the synthesis method resulted in the formation of a yellow fine-crystalline precipitate. The structure and nature of ligand coordination with the metal ion were confirmed by physicochemical methods (electron and vibrational spectroscopy) and semi-empirical quantum chemical calculations (MOPAC//PM7). Electronic spectroscopy records a significant bathochromic shift (Δλ=72 nm). It indicates the formation of a stable complex. The research reveals the dependence of the complex stability on the pH of the medium, and identifies the its optimal pH range of 7.0–8.0. The theoretical part of the research includes quantum chemical modeling to evaluate the redistribution of electron density, and visualise the optimised geometry of the molecule. Moreover, computer analysis of biological activity and pharmacokinetic parameters (ADME-Tox) indicates the potential value of the synthesized complex as a compound with a modified and improved biological activity profile.
8-oxyquinoline, IR spectroscopy, electron spectroscopy, lanthanum, complex formation, coordination number, complex stability, PASS-online
1. Bhagwat A., Butts A., Greve E., Cheung Y., Melief E., Gomez J., Hung D.T., Parish T. 8-Hydroxyquinoline series exerts bactericidal activity against Mycobacterium tuberculosis via copper-mediated toxicity. ACS Infect. Dis. 2024, 10(10), 3692–3698. DOI:https://doi.org/10.1021/acsinfecdis.4c00582. EDN: https://elibrary.ru/ENZRKF
2. Cipurković A., Horozić E., Marić S., Mekić L., Junuzović H. Metal Complexes with 8-Hydroxyquinoline: Synthesis and In Vitro Antimicrobial Activity. Open J. Appl. Sci. 2021, 11, 1–10. DOI:https://doi.org/10.4236/ojapps.2021.111001.
3. Elshahed M.S., Toubar S.S., Ashour A.A., El-Eryan R.T. Novel sensing probe using Terbium-sensitized luminescence and 8-hydroxyquinoline for determination of prucalopride succinate: green assessment with Complex-GAPI and analytical Eco-Scale. BMC Chem. 2022, 16(1), 80. DOI: https://doi.org/10.1186/s13065-022-00876-0 EDN: https://elibrary.ru/ORMZSY
4. Avetisov R., Kazmina K., Barkanov A. One-Step Synthesis of High-Pure Tris(8-hydroxyquinoline)aluminum for Optics and Photonics. Materials. 2022, 15, 734. DOI:https://doi.org/10.3390/ma15030734 EDN: https://elibrary.ru/WABIQW
5. Ribeiro N., Bulut I., Ugone V., Ferreira L.P. Promising anticancer agents based on 8-hydroxyquinoline: coordination to metal ions fosters cytotoxic activity. Front. Chem. 2023, 11, 1106349. DOI:https://doi.org/10.3389/fchem.2023.1106349. EDN: https://elibrary.ru/EGWFMC
6. Côrte-Real L., Martins M., Fontrodona X. Cu(II) and Zn(II) Complexes of New 8-Hydroxyquinoline Schiff Bases: Structure, Speciation, and Anticancer Potential. Molecules 2023, 28, 7894. DOI:https://doi.org/10.3390/molecules28107894. DOI: https://doi.org/10.3390/molecules28237894; EDN: https://elibrary.ru/MCGWCT
7. Lopes J., Romero I., Correia I., Gaspar M.M. Novel 8-Hydroxyquinoline-Derived V(IV)O, Ni(II), and Fe(III) Complexes: Synthesis, Characterization, and Cytotoxicity. Inorganics 2025, 13, 150. DOI:https://doi.org/10.3390/2304-6740/13/5/150. DOI: https://doi.org/10.3390/inorganics13050150; EDN: https://elibrary.ru/ZERVTS
8. Wu D.-F., Liu Z., Ren P., Liu X.-H., Wang N., Cui J.-Z., Gao H.-L. A new family of dinuclear lanthanide complexes constructed from an 8-hydroxyquinoline Schiff base and β-diketone: magnetic properties and near infrared luminescence. Dalton Trans. 2019, 48, 1392-1403. DOI:https://doi.org/10.1039/C8DT04384A.
9. Saadeh H.A., Sweidan K.A., Mubarak M.S. Recent Advances in the Synthesis and Biological Activity of 8 Hydroxyquinolines. Molecules 2020, 25(18), 4321. DOI:https://doi.org/10.3390/molecules25184321. EDN: https://elibrary.ru/GRNBDC
10. Ramenskaya, L. M., Vladimirova, T. V. The stability and solubility of cadmium (II)-8-oxyquinoline complexes in water and micellar solutions of sodium dodecyl sulfate. Russ. J. Phys. Chem., 2006, 80(6), 904-908. DOI: https://doi.org/10.1134/S0036024406060112. EDN: https://elibrary.ru/LJNVTL
11. Chupakhina, T. A., Katsev, A. M., Kuryanov, V. O. Synthesis and investigation of antimicrobial activity of 8 Hydroxyquinoline glucosaminides. Russian J. of Bioorg. Chem. 2012, 38(4), 422-427. DOI: https://doi.org/10.1134/S106816201204005X EDN: https://elibrary.ru/XKLWDZ
12. Ninh, N. H., Sang, D. X. N., Hieu, D. M., Chi, N. T. T. Anti-microbial activity of some Pt (II) complexes bearing 8-oxyquinoline (8-OQ) and eugenol derivative and 3D-structure of complex [PtCl (8-OQ)(Eugenol)]. J. Nat. Sci., 2024, 118-124. DOI: https://doi.org/10.18173/2354-1059.2024-0026 EDN: https://elibrary.ru/QQHBEY
13. Al-Farhan B.S., Basha M.T., Abdalla E.M. Synthesis, DFT Calculations, Antiproliferative, Bactericidal and Antioxidant Activities of Mixed-Ligand Metal Complexes Containing 8-Hydroxyquinoline. Molecules 2021, 26(16), 4725. DOI:https://doi.org/10.3390/molecules26164725. EDN: https://elibrary.ru/GHKSFO
14. Yu, W. Y., Zhang, L. G., Qiu, J. B., Wang, J. X., Chen, C. J., Zhou, M. G. Effect of carbendazim-8-oxyquinoline-copper, a novel chelate fungicide against Fusarium graminearum. J. of Pest. Sci., 2011, 36(3), 385-391. DOI: https://doi.org/10.1584/jpestics.G11-15
15. Yabrir B., Belhassan A., Laklifi T., Moran S. G., Buakhrin M., Kandiya G. L. Determination inhibitors of the main protease of SARS-CoV-2 in trace amounts of components of Algerian herbal medicines using in silico methods. Pharmacy and pharmacology. 2025, 13 (1), 56-66. DOI:https://doi.org/10.19163/2307-9266-2025-13-1-56-66 EDN: https://elibrary.ru/SFGKIP
16. Zhang L., Shi H., Jiang Z. Ten-Gram-Scale Mechanochemical Synthesis of Ternary Lanthanum Coordination Polymers for Antibacterial and Antitumor Activities. Front. Chem. 2022, 10:898324. DOI:https://doi.org/10.3389/fchem.2022.898324. EDN: https://elibrary.ru/PSVXPV
17. Zhou X. Insights of metal 8-hydroxylquinolinol complexes as the potential anticancer drugs. J. Inorg. Biochem. 2023, 238, 112051. DOI:https://doi.org/10.1016/j.jinorgbio.2022.112051. EDN: https://elibrary.ru/QRWLPS
18. Gallo E. Aluminium 8-Hydroxyquinolinate N-Oxide as a Precursor to Heterometallic Complexes: Synthesis and Characterization. Molecules. 2024, 29(2), 451. DOI:https://doi.org/10.3390/molecules29020451. EDN: https://elibrary.ru/SCIMLD
19. He J., Zhou T., Cao Y., Zhang Y., Yang W., Ma M. Study on relationship between fluorescence properties and structure of substituted 8-hydroxyquinoline zinc complexes. J. Fluorescence 2018. DOI:https://doi.org/10.1007/s10895-018-2275-7.
20. General Pharmacopoeia Article .1.2.1.0005.15 Solubility. The State Pharmacopoeia of the Russian Federation [Electronic resource]. Available at: https://pharmacopoeia.regmed.ru/ (accessed: 22.11.2025)
21. Schollenberger C. J. Ammonium acetate as a neutral buffered standard. J. Am. Chem. Soc. 1932, 54(6), 2568-2573. DOI: https://doi.org/10.1021/ja01345a515.
22. Mandal, P., Kretzschmar, J., Drobot, B. Not just a background: pH buffers do interact with lanthanide ions—a Europium (III) case study. JBIC J. of Biol. Inorg. Chem. 2022. 27(2), 249-260. DOI: https://doi.org/10.1007/s00775-022-01930-x EDN: https://elibrary.ru/DMIESX
23. Kothawade, S., Shende, P. Coordination bonded stimuli-responsive drug delivery system of chemical actives with metal in pharmaceutical applications. Coord. Chem. Rev. 2024, 510, 215851. DOI: https://doi.org/10.1016/j.ccr.2024.215851. EDN: https://elibrary.ru/DBFDRW
24. James J. P. Stewart, MOPAC2016, Stewart Computational Chemistry, Colorado Springs, CO, USA. Available at: http://openmopac.net/ (accessed: 22.11.2025)
25. Zhurko G.A., Zhurko D.A. ChemCraft version 1.6 (build 312). Available at: http://www.chemcraftprog.com/index.html (accessed: 22.11.2025)
26. Filimonov D.A., Lagunin A.A., Gloriozova T.A., Rudik A.V., Druzhilovskii D.S., Pogodin P.V., Poroikov V.V. Prediction of the biological activity spectra of organic compounds using the PASS online web resource. Chemistry of Heterocyclic Compounds. 2014, 50(3), 444-457. DOI: https://doi.org/10.1007/s10593-014-1496-1 EDN: https://elibrary.ru/UEKHWB
27. ChemAxon Log D vs. pH Predictor. ChemAxon. Available at: https://chemaxon.com/products/logd-predictor (accessed: 22.11.2025).
28. Daina A., Michielin O., Zoete V. SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci. Rep. 2017, 7, 12717. DOI: https://doi.org/10.1038/srep42717 EDN: https://elibrary.ru/YZSVSD
29. Odhiambo, D. O., Omosa, L. K., Njagi, E. C., Kithure, J. G., Wekesa, E. N. In-silico Pharmacokinetics ADME/Tox Analysis of phytochemicals from genus Dracaena for their therapeutic potential. Sci. Afr. 2025, e02796. DOI: https://doi.org/10.1016/j.sciaf.2025.e02796 EDN: https://elibrary.ru/SROPLZ
30. Yadav, M., Yadav, P., Yadav, J. P., & Kataria, S. K. Novel derivatives of Costus igneus towards potentiality against diabetes mellitus receptors: ADME/Tox profiling, Computational Docking, and Molecular Dynamics Simulation study. J. of Taibah Univ. for Sci. 2024, 18(1), 2370107. DOI: https://doi.org/10.1080/16583655.2024.2370107.
31. Ahmad, I., Dogra, A., Nagpal, T., Sharma, C., Singh, S., Shaiva, N., Luhach, K. Liposome-like encapsulation of fish oil-based self-nano emulsifying formulation for improved bioavailability. Appl. Food Res., 2025, 5(1), 100745. DOI: https://doi.org/10.1016/j.afres.2025.100745. EDN: https://elibrary.ru/PFDHTT



