Fe(III), Co(III), and Cu(II) Complexes with Acylhydrazones Containing a Triphenylphosphonium Moiety: Synthesis, Crystal Structure, and Antibacterial Activity
- Авторлар: Matiukhina A.K.1, Zorina-Tikhonova E.N.1, Gogoleva N.V.1, Popov L.D.2, Morozov P.G.2, Lazarenko V.A.3, Zubenko A.A.4, Fetisov L.N.4, Svyatogorova A.E.4, Kiskin M.A.1, Eremenko I.L.1
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Мекемелер:
- Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences
- Southern Federal University
- National Research Center “Kurchatov Institute”
- North Caucasus Zonal Research Veterinary Institute, Branch, Federal Rostov Agrarian Research Center
- Шығарылым: Том 51, № 6 (2025)
- Беттер: 387-399
- Бөлім: Articles
- URL: https://ruspoj.com/0132-344X/article/view/687260
- DOI: https://doi.org/10.31857/S0132344X25060047
- EDN: https://elibrary.ru/KINTIN
- ID: 687260
Дәйексөз келтіру
Аннотация
New acylhydrazones based on para- and meta-nitrobenzhydrazides and substituted salicylic aldehyde containing a triphenylphosphonium fragment were synthesized and spectrally characterized. With these acylhydrazones, a series of new mononuclear coordination compounds of Fe(III), Co(III), and Cu(II) were obtained, the molecular structure of which was determined by single-crystal X-ray diffraction. The antibacterial activity of the isolated acylhydrazones and copper(II) complexes against Staphylococcus aureus and Escherichia coli was studied. It was shown that the transition from an organic compound to a complex one contributes to a significant increase in activity against E. coli.
Толық мәтін

Авторлар туралы
A. Matiukhina
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences
Email: ezorinatikhonova@igic.ras.ru
Ресей, Moscow
E. Zorina-Tikhonova
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: ezorinatikhonova@igic.ras.ru
Ресей, Moscow
N. Gogoleva
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences
Email: ezorinatikhonova@igic.ras.ru
Ресей, Moscow
L. Popov
Southern Federal University
Email: ezorinatikhonova@igic.ras.ru
Ресей, Rostov-on-Don
P. Morozov
Southern Federal University
Email: ezorinatikhonova@igic.ras.ru
Ресей, Rostov-on-Don
V. Lazarenko
National Research Center “Kurchatov Institute”
Email: ezorinatikhonova@igic.ras.ru
Ресей, Moscow
A. Zubenko
North Caucasus Zonal Research Veterinary Institute, Branch, Federal Rostov Agrarian Research Center
Email: ezorinatikhonova@igic.ras.ru
Ресей, Novocherkassk
L. Fetisov
North Caucasus Zonal Research Veterinary Institute, Branch, Federal Rostov Agrarian Research Center
Email: ezorinatikhonova@igic.ras.ru
Ресей, Novocherkassk
A. Svyatogorova
North Caucasus Zonal Research Veterinary Institute, Branch, Federal Rostov Agrarian Research Center
Email: ezorinatikhonova@igic.ras.ru
Ресей, Novocherkassk
M. Kiskin
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences
Email: ezorinatikhonova@igic.ras.ru
Ресей, Moscow
I. Eremenko
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences
Email: ezorinatikhonova@igic.ras.ru
Ресей, Moscow
Әдебиет тізімі
- Larsson D.G.J., Flach C.-F. // Nat. Rev. Microbiol. 2022. V. 20. P. 257. https://doi.org/10.1038/s41579-021-00649-x
- Darby E.M., Trampari E., Siasat P. et al. // Nat. Rev. Microbiol. 2024. V. 21. P. 280. https://doi.org/10.1038/s41579-022-00820-y
- Lucien M.A.B., Canarie M.F., Kilgore P.E. et al. // Int. J. Infect. Dis. 2021. V. 104. P. 250. https://doi.org/10.1016/j.ijid.2020.12.087
- Ding D., Wang B., Zhang X. et al. // Ecotoxicol. Environ. Saf. V. 254. P. 114734. https://doi.org/10.1016/j.ecoenv.2023.114734
- Vlad I.M., Nuță D.C., Căproiu M.T. et al. // Antibiotics. 2024. V. 13. № 3. P. 212. https://doi.org/10.3390/antibiotics13030212
- Sharma P.C., Sharma D., Sharma A. et al. // Mater. Today Chem. 2020. V. 18. P. 100349. https://doi.org/10.1016/j.mtchem.2020.100349
- Matiukhina A.K., Vladimirova А.E., Zorina-Tikhonova Е.N. et al. // Russ. J. Gen. Chem. 2023. V. 93 № 2. P. S596. https://doi.org/10.1134/S1070363223150276
- Czyżewska I., Mazur L., Popiołek Ł. // Chem. Biol. Drug Des. 2024. V. 104. № 1. P. e14590. https://doi.org/10.1111/cbdd.14590
- Deng J., Gou Y., Chen W. // Bioorg. Med. Chem. 2016. V. 24. № 10. P. 2190. https://doi.org/10.1016/j.bmc.2016.03.033
- Chimmalagi G.H., Kendur U., Patil S.M. et al. // Appl. Organomet. Chem. 2018. V. 32. № 6. P. e4337. https://doi.org/10.1002/aoc.4337
- Fekri R., Salehi M., Asadi A., Kubicki M. // Appl. Organomet. Chem. 2018. V. 32. № 2, P. e4019. https://doi.org/10.1002/aoc.4019
- Chimmalagi G.H., Kendur U., Patil S.M. et al. // Appl. Organomet. Chem. 2019. V. 33. № 1. P. e4557. https://doi.org/10.1002/aoc.4557
- Jansová H., Kubeš J., Reimerová P. et al. // Chem. Res. Toxicol. 2018. V. 31. № 11. P. 1151. https://doi.org/10.1021/acs.chemrestox.8b00165
- Bashir M., Dar A.A., Yousuf I. // ACS Omega. 2023. V. 8. № 3. P. 3026. https://doi.org/10.1021/acsomega.2c05927
- Jing C., Wang C., Yan K. et al. // Bioorg. Med. Chem. 2016. V. 24. № 2. P. 270. https://doi.org/10.1016/j.bmc.2015.12.013
- Hamzi I. // Mini-Rev. Org. Chem. 2022. V. 19. № 8. P. 968. https://doi.org/10.2174/1570193x19666220328124048
- Thota S., Rodrigues D.A., Pinheiro P.S.M. et al. // Bioorg. Med. Chem. Lett. 2018. V. 28. № 17. P. 2797. https://doi.org/10.1016/j.bmcl.2018.07.015
- Asadi Z., Haddadi E., Sedaghat M. // J. Photochem. Photobiol. A. 2017. V 337. P. 140. https://doi.org/10.1016/j.jphotochem.2017.01.022
- Li Y., Yang Z., Zhou M. et al. // RSC Adv. 2017. V. 7. P. 41527. https://doi.org/10.1039/c7ra05504h
- Li Y., Yang Z., Zhou M., Lia Y. // RSC Adv. 2017. V. 7. P. 49404. https://doi.org/10.1039/c7ra10283f
- Lauria A., Bonsignore R., Terenzi A. et al. // Dalton Trans. 2014. V. 43. P. 6108. https://doi.org/10.1039/c3dt53066c
- Anastasiadou D., Psomas G., Kalogiannis S. et al. // J. Inorg. Biochem. 2019. V. 198. P. 110750. https://doi.org/10.1016/j.jinorgbio.2019.110750
- Burlov A.S., Vlasenko V.G., Chal’tsev B.V. et al. // Russ. J. Coord. Chem. 2021. V. 47. P. 439. https://doi.org/10.1134/s1070328421070010
- Stadler A.-M., Harrowfield J. // Inorg. Chim. Acta. 2009. V. 362. № 12. P. 4298. https://doi.org/10.1016/j.ica.2009.05.062
- Murphy M.P., Smith R.A.J. // Annu. Rev. Pharmacol. Toxicol. 2007. V. 47. P. 629. https://doi.org/10.1146/annurev.pharmtox.47.120505. 105110
- Milenković M.R., Živković-Radovanović V., Andjelković L. // Russ. J. Gen. Chem. 2020. V. 90, P. 1716. https://doi.org/10.1134/s1070363220090194
- Lee S.K., Tan K.W., Ng S.W. et al. // Spectrochim. Acta. A. 2014. V. 121. P. 101. https://doi.org/10.1016/j.saa.2013.10.084
- Sheldrick G.M. SADABS. Madison (WI, USA): Bruker AXS Inc., 1996.
- Svetogorov R.D., Dorovatovskii P.V., Lazarenko V.A. // Cryst. Res. Technol. 2020. V. 55. № 5. P. 1900184. https://doi.org/10.1002/crat.201900184
- Lazarenko V.A., Dorovatovskii P.V., Zubavichus Y.V. et al. // Crystals. 2017. V. 7. № 11. P. 325. https://doi.org/10.3390/cryst7110325
- Kabsch W. // Acta Crystallogr. D. 2010. V. 66. № 2. P. 125. https://doi.org/10.1107/S0907444909047337
- Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. № 1. P. 3. https://doi.org/10.1107/S2053273314026370
- Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. № 1. P. 3. https://doi.org/10.1107/S2053229614024218
- Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339. https://doi.org/10.1107/S0021889808042726
- Spek A.L. // Acta Crystallogr. C. 2015. V. 71. P. 9. https://doi.org/10.1107/S2053229614024929
- Llunell M., Casanova D., Cirera J. et al. SHAPE, v.2.1, Program for the stereochemical analysis of molecular fragments by means of continuous shape measures and associated tools. Barcelona (Spain): Universitat de Barcelona, 2013.
- Scarlett N.V.Y., Madsen I.C. // Powder Diffr. 2006. V. 21. № 4. P. 278. https://doi.org/10.1154/1.2362855
- Adam M.S.S., Alghanim A.S.I., Abualreish M.J.A. et al. // Appl. Organomet. Chem. 2024. V. 38. № 4. Art. e7394. https://doi.org/10.1002/aoc.7394
- Yan Y.-B., Yang R.-W., Zhang H.-W. et al. // J. Mol. Struct. 2024. V. 1299. P. 137148. https://doi.org/10.1016/j.molstruc.2023.137148
- El-Sherif A.A., Fetoh A., Abdulhamed Y.Kh., Abu El-Reash G.M. // Inorg. Chim. Acta. 2018. V. 480. P. 1. https://doi.org/10.1016/j.ica.2018.04.038
- Adly O.M.I., Taha A., Ibrahim M.A. // Appl. Organomet. Chem. 2022. V. 36. № 3. Art. e6558. https://doi.org/10.1002/aoc.6558
- Alkhatib F.M., Alsulami H.M. // Heliyon. 2023. V. 9. № 8. Art. e18988. https://doi.org/10.1016/j.heliyon.2023.e18988
- Ahmed M.A., Zhernakov M.A., Gilyazetdinov E.M. et al. // Inorganics. 2023. V. 11. № 4. P. 167. https://doi.org/10.3390/inorganics11040167
- El-Gammal O.A., Abu El-Reash G.M., Bedier R.A. // Appl. Organomet. Chem. 2019. V. 33. № 10. Art. e5141. https://doi.org/10.1002/aoc.5141
- Bellamy L.J. The Infrared Spectra of Complex Molecules. Springer Dordrecht. Chapman and Hall, London, 1980. https://doi.org/10.1007/978-94-011-6520-4
- Hashem H.E., Mohamed E.A., Farag A.A. et al. // Appl. Organomet. Chem. 2021. V. 35. № 9. Art. e6322. https://doi.org/10.1002/aoc.6322
- Edwards D.A., Richards R. // Spectrochim Acta. A. 1978. V. 34. № 2. P. 167. https://doi.org/ 10.1016/0584-8539(78)80111-1
- Huang D.-S., Liu X.-R., Zhao S.-S., Yang Z.-W. // Polyhedron. 2022. V. 211. P. 115516. https://doi.org/10.1016/j.poly.2021.115516
- Chang L.-L., Yang J., Lai S.-Q. et al. // Inorg. Chim. Acta. 2022. V. 532. P. 120751. https://doi.org/10.1016/j.ica.2021.120751
- Dinku D., Demissie T.B., Beas I.N. et al. // Inorg. Chem. Commun. 2024. V. 160. P. 111903. https://doi.org/10.1016/j.inoche.2023.111903
- Shakdofa M.M.E., Al-Hakimi A.N., Elsaied F.A. et al. // Bull. Chem. Soc. Ethiop. 2017. V. 31. № 1. P. 75. https://doi.org/10.4314/bcse.v31i1.7
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