- PII
- S0132344X25060047-1
- DOI
- 10.31857/S0132344X25060047
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 51 / Issue number 6
- Pages
- 387-399
- Abstract
- 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.
- Keywords
- ацилгидразоны нитробензгидразиды трифенилфосфоний комплексы 3d-металлов антибактериальная активность
- Date of publication
- 14.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 3
References
- 1. Larsson D.G.J., Flach C.-F. // Nat. Rev. Microbiol. 2022. V. 20. P. 257. https://doi.org/10.1038/s41579-021-00649-x
- 2. 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
- 3. 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
- 4. Ding D., Wang B., Zhang X. et al. // Ecotoxicol. Environ. Saf. V. 254. P. 114734. https://doi.org/10.1016/j.ecoenv.2023.114734
- 5. Vlad I.M., Nuță D.C., Căproiu M.T. et al. // Antibiotics. 2024. V. 13. № 3. P. 212. https://doi.org/10.3390/antibiotics13030212
- 6. 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
- 7. 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
- 8. Czyżewska I., Mazur L., Popiołek Ł. // Chem. Biol. Drug Des. 2024. V. 104. № 1. P. e14590. https://doi.org/10.1111/cbdd.14590
- 9. 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
- 10. 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
- 11. Fekri R., Salehi M., Asadi A., Kubicki M. // Appl. Organomet. Chem. 2018. V. 32. № 2, P. e4019. https://doi.org/10.1002/aoc.4019
- 12. 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
- 13. 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
- 14. Bashir M., Dar A.A., Yousuf I. // ACS Omega. 2023. V. 8. № 3. P. 3026. https://doi.org/10.1021/acsomega.2c05927
- 15. 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
- 16. Hamzi I. // Mini-Rev. Org. Chem. 2022. V. 19. № 8. P. 968. https://doi.org/10.2174/1570193x19666220328124048
- 17. 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
- 18. 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
- 19. Li Y., Yang Z., Zhou M. et al. // RSC Adv. 2017. V. 7. P. 41527. https://doi.org/10.1039/c7ra05504h
- 20. Li Y., Yang Z., Zhou M., Lia Y. // RSC Adv. 2017. V. 7. P. 49404. https://doi.org/10.1039/c7ra10283f
- 21. Lauria A., Bonsignore R., Terenzi A. et al. // Dalton Trans. 2014. V. 43. P. 6108. https://doi.org/10.1039/c3dt53066c
- 22. 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
- 23. 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
- 24. Stadler A.-M., Harrowfield J. // Inorg. Chim. Acta. 2009. V. 362. № 12. P. 4298. https://doi.org/10.1016/j.ica.2009.05.062
- 25. 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
- 26. Milenković M.R., Živković-Radovanović V., Andjelković L. // Russ. J. Gen. Chem. 2020. V. 90, P. 1716. https://doi.org/10.1134/s1070363220090194
- 27. 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
- 28. Sheldrick G.M. SADABS. Madison (WI, USA): Bruker AXS Inc., 1996.
- 29. 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
- 30. Lazarenko V.A., Dorovatovskii P.V., Zubavichus Y.V. et al. // Crystals. 2017. V. 7. № 11. P. 325. https://doi.org/10.3390/cryst7110325
- 31. Kabsch W. // Acta Crystallogr. D. 2010. V. 66. № 2. P. 125. https://doi.org/10.1107/S0907444909047337
- 32. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. № 1. P. 3. https://doi.org/10.1107/S2053273314026370
- 33. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. № 1. P. 3. https://doi.org/10.1107/S2053229614024218
- 34. 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
- 35. Spek A.L. // Acta Crystallogr. C. 2015. V. 71. P. 9. https://doi.org/10.1107/S2053229614024929
- 36. 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.
- 37. Scarlett N.V.Y., Madsen I.C. // Powder Diffr. 2006. V. 21. № 4. P. 278. https://doi.org/10.1154/1.2362855
- 38. 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
- 39. 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
- 40. 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
- 41. 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
- 42. Alkhatib F.M., Alsulami H.M. // Heliyon. 2023. V. 9. № 8. Art. e18988. https://doi.org/10.1016/j.heliyon.2023.e18988
- 43. Ahmed M.A., Zhernakov M.A., Gilyazetdinov E.M. et al. // Inorganics. 2023. V. 11. № 4. P. 167. https://doi.org/10.3390/inorganics11040167
- 44. 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
- 45. 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
- 46. 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
- 47. Edwards D.A., Richards R. // Spectrochim Acta. A. 1978. V. 34. № 2. P. 167. https://doi.org/ 10.1016/0584-8539(78)80111-1
- 48. 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
- 49. 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
- 50. 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
- 51. 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
