- PII
- 10.31857/S0044457X22601651-1
- DOI
- 10.31857/S0044457X22601651
- Publication type
- Status
- Published
- Authors
- Volume/ Edition
- Volume 68 / Issue number 3
- Pages
- 342-348
- Abstract
- The equilibria of stepwise substitution Au(bipy) + OH– = Au(bipy)ClOH+ + Cl– and Au(bipy) + 2OH– = Au(bipy) + 2Cl– in aqueous solution at T = 25°C and I = 0.2 M (NaCl), log β1 = 9.22, log β2 = 16.61 have been studied. For bipyridyl complexes Au(bipy) (X = Cl, OH) at pH 2.0 and 7.4, redox interactions with anions of thiol-containing acids (glutathione, cysteine, thiomalate) have been studied. In all cases, at the initial stage, a rapid reduction of gold(III) to gold(I) was observed with the simultaneous release of bipyridyl. A detailed analysis of UV spectra showed that the main products of gold(III) reduction are highly stable gold(I) thiolate complexes. The presence of further slower steps depends on the initial ratio of thiol to gold.
- Keywords
- азотсодержащие лиганды комплексообразование глутатион цистеин тиомалат
- Date of publication
- 17.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 13
References
- 1. Brinas R.P., Hu M., Qian L. et al. // J. Am. Chem. Soc. 2008. V. 130. P. 975. https://doi.org/10.1021/ja076333e
- 2. Corthey G., Giovanetti L.J., Ramallo-Lopez J.M. et al. // ACS Nano. 2010. V. 4. P. 3413. https://doi.org/10.1021/nn100272q
- 3. Brown D.H., Smith W.E. // J. Chem. Soc., Dalton Trans. 1980. P. 217.
- 4. Gabbiani C., Casini A., Messori L. // Gold Bull. 2007. V. 40. P. 73. https://doi.org/10.1007/BF03215296
- 5. Radisavljević S., Petrović B. // Front. Chem. 2020. V. 8. P. 379. https://doi.org/10.3389/fchem.2020.00379
- 6. Alhoshani A., Sulaiman A.A.A., Sobeai H.M.A. et al. // Molecules. 2021. V. 26. P. 3973. https://doi.org/10.3390/molecules26133973
- 7. Mironov I.V., Kharlamova V.Yu. // Inorg. Chim. Acta. 2021. V. 525. P. 120500. https://doi.org/10.1016/j.ica.2021.120500
- 8. Миронов И.В., Харламова В.Ю. // Журн. неорган. химии. 2022. Т. 67. № 7. С. 972.
- 9. Nobili S., Mini E., Landini I. et al. // Med. Res. Rev. 2010. V. 30. № 3. P. 550. https://doi.org/10.1002/med.20168
- 10. Mironov I.V., Kharlamova V.Yu. // J. Solution Chem. 2020. V. 49. P. 583. https://doi.org/10.1007/s10953-020-00994-0
- 11. Ахмадуллина Н.С., Чураков А.В., Ретивов В.М и др. // Коорд. химия. 2012. Т. 38. № 9. С. 611.
- 12. Avdeeva V.V., Vologzhanina A.V., Kubasov A.S. et al. // Inorganics. 2022. V. 10. P. 99. https://doi.org/10.3390/inorganics10070099
- 13. Harned H.S., Owen B.B. The Physical Chemistry of Electrolytic Solutions. N.Y.: Reinhold, 1950.
- 14. Mironov I.V., Kharlamova V.Yu. // J. Solution Chem. 2018. V. 47. P. 511. https://doi.org/10.1007/s10953-018-0735-y
- 15. Jakusch T., Buglyó P., Tomaz A.I. et al. // Inorg. Chim. Acta. 2002. V. 339. P. 119. https://doi.org/10.1016/S0020-1693 (02)00919-2
- 16. LeBlanc D.J., Smith R.W., Wang Z. et al. // J. Chem. Soc., Dalton Trans. 1997. V. 18. P. 3263. https://doi.org/10.1039/A700827I
- 17. Đurović M.D., Bugarčić Ž.D., Heinemann F.W., Eldik R. // Dalton Trans. 2014. V. 43. P. 3911. https://doi.org/10.1039/C3DT53140F
- 18. Liu Y., Tian H., Xu L. et al. // Int. J. Mol. Sci. 2019. V. 20. P. 5660. https://doi.org/10.3390/ijms20225660
- 19. Brown D.H., Paton M., Smith W.E. // Inorg. Chim. Acta. 1982. V. 66. P. L51.
- 20. 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
- 21. Messori L., Marcon G., Orioli P. // Bioinorg. Chem. Appl. 2003. V. l. № 2. P. 177. https://doi.org/10.1155/S1565363303000141
- 22. Marcon G., Carotti S., Coronnello M. et al. // J. Med. Chem. 2002. V. 45. P. 1672. https://doi.org/10.1021/jm010997w