- PII
- 10.31857/S0044457X24100125-1
- DOI
- 10.31857/S0044457X24100125
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 69 / Issue number 10
- Pages
- 1459-1465
- Abstract
- The interaction of gold(III) complexes AuCl4–, Au(bipy)Cl2+, Au(en)23+ and Au(C9H19N4)2+ with methionine (HMet) in an aqueous solution (pH 2.0 и 7.4; I = 0.2 M (NaCl), CAu = (5–10) × 10–5 M, CHMet < (6–50) × 10–5 M) at 25°C was studied. Methionine reduces gold(III) to gold(I), but the processes proceed much more slowly (hundreds of times) than under the action of thiols. As the density of ligands in the gold(III) complex increases, the rate of reactions with HMet decreases significantly.
- Keywords
- соединения золота(III) редокс-процессы метионин глутатион
- Date of publication
- 17.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 11
References
- 1. Casini A., Kelter G., Gabbiani C. et al. // J. Biol. Inorg. Chem. 2009. V. 14. P. 1139. https://doi.org/10.1007/s00775-009-0558-9
- 2. Brown D.H., Smith W.E. // Chem. Soc. Rev. 1980. V. 9. P. 217. https://doi.org/10.1039/CS9800900217
- 3. Fricker S.P. // Gold Bull. 1996. V. 29. P. 53. https://doi.org/10.1007/BF03215464
- 4. Gorini G., Magherini F., Fiaschi T. et al. // Biomedicines. 2021. V. 9. P. 871. https://doi.org/10.3390/biomedicines9080871
- 5. Tong K.-C., Hu D., Wan P.-K. et al. // Front. Chem. 2020. V. 8. P. 587207. https://doi: 10.3389/fchem.2020.587207
- 6. Gabbiani C., Casini A., Messori L. // Gold Bull. 2007. V. 40. P. 73. https://doi.org/10.1007/BF03215296
- 7. Glišić B.Đ., Rychlewska U., Djuran M.I. // Dalton Trans. 2012. V. 41. P. 6887. https://doi.org/10.1039/C2DT30169E
- 8. Mironov I.V., Kharlamova V.Yu. // ChemistrySelect. 2023. V. 8. P. e202301337. https://doi.org/10.1002/slct.202301337
- 9. Миронов И.В., Харламова В.Ю. // Журн. неорган. химии. 2023. Т. 68. № 10. С. 1495. https://doi.org/10.31857/S0044457X23600639
- 10. Миронов И.В., Харламова В.Ю., Ху Ц. // Журн. неорган. химии. 2023. Т. 68. № 3. С. 342. https://doi.org/10.31857/S0044457X22601651
- 11. Block B.P., Bailar J.C. // J.Am. Chem. Soc. 1951. V. 73. P. 4722. https://doi.org/10.1021/ja01154a071
- 12. Brawner S.A., Lin I.J.B., Kim J.-H., Everett Jr.G.W. // Inorg. Chem. 1978. V. 17. P. 1304. https://doi.org/10.1021/ic50183a040
- 13. Миронов И.В., Харламова В.Ю. // Журн. неорган. химии. 2017. Т. 62. № 12. С. 1672. https://doi.org/10.7868/S0044457X17120182
- 14. Миронов И.В., Харламова В.Ю. // Журн. неорган. химии. 2017. Т. 62. № 7. С. 1014. https://doi.org/10.7868/S0044457X17070157
- 15. Vujačić A.V., Savić J.Z., Sovilj S.P. et al. // Polyhedron. 2009. V. 28. P. 593. https://doi.org/10.1016/j.poly.2008.11.045
- 16. Glišić B.Đ., Rajković S., Stanić Z.D., Djuran M.I. // Gold Bull. 2011. V. 44. P. 91. https://doi.org/10.1007/s13404-011-0014-9
- 17. Bordignon E., Cattalini L., Natile G., Scatturin A. // J. Chem. Soc., Chem. Commun. 1973. P. 878. https://doi.org/10.1039/C39730000878
- 18. Glišić B.Đ., Djuran M.I., Stanić Z.D., Rajković S. // Gold Bull. 2014. V. 47. P. 33. https://doi.org/10.1007/s13404-013-0108-7
- 19. Al-Maythalony B.A., Wazeer M.I.M., Isab A.A., Ahmad S. // Spectroscopy. 2010. V. 24. P. 567. https://doi.org/10.3233/SPE-2010-0478
- 20. Ericson A., Elding L.I., Elmroth S.K.C. // J. Chem. Soc., Dalton Trans. 1997. P. 1159. https://doi.org/10.1039/A608001D
- 21. Annibale G., Canovese L., Cattalini L., Natile G. // J. Chem. Soc., Dalton Trans. 1980. P. 1017. https://doi.org/10.1039/DT9800001017
- 22. Al-Maythalony B.A., Wazeer M.I.M., Isab A.A. // Inorg. Chim. Acta. 2010. V. 363. P. 3244. https://doi.org/10.1016/j.ica.2010.06.001
- 23. Đurović M.D., Bugarčić Ž.D., Heinemann F.W., Eldik R. // Dalton Trans. 2014. V. 43. P. 3911. https://doi.org/10.1039/C3DT53140F
- 24. Stadtman E.R, Moskovitz J., Levine R.L. // Antioxid. Redox Signal. 2003. V. 5. P. 577. https://doi.org/10.1089/152308603770310239
