Cationic—Anionic Pd(II) Complexes with Adamantylimidazolium Cation: Synthesis, Structural Study, and MAO-Inhibiting Activity
- Авторы: Denisov M.S.1, Dmitriev M.V.2, Eroshenko D.V.1, Slepukhin P.A.3,4, Shavkunov S.P.2, Glushkov V.A.1,2
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Учреждения:
- Institute of Technical Chemistry, Ural Branch
- Perm State University
- Ural State Technical University
- Postovskii Institute of Organic Synthesis, Ural Branch
- Выпуск: Том 64, № 1 (2019)
- Страницы: 56-67
- Раздел: Coordination Compounds
- URL: https://journals.rcsi.science/0036-0236/article/view/169203
- DOI: https://doi.org/10.1134/S0036023619010054
- ID: 169203
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Аннотация
New cationic-anionic palladium(II) complexes have been prepared from adamantyl-substituted imidazolium salts and effect of structure of the adamantyl-substituted salts and synthesis conditions on the structure of these complexes with \({\rm{Pd}}({\rm{DMSO}}){\rm{Hal}}_3^ - \) (1–4), \({\rm{P}}{{\rm{d}}_2}{\rm{Br}}_6^{2 - }\) (5, 6), or \({\rm{PdCl}}_4^{2 - }\) (7) anions has been studied. A number of palladium(II) complexes active against monoamine oxidase B has been prepared, effect of composition and structure on their biological activity have been revealed. The structure of the complexes has been confirmed by X-ray diffraction analysis, a conductometric study of complex 1 has been performed. MAO-inhibiting activity of the obtained complexes has been found to be on the level of reference compounds: 17.6% of residual enzyme activity upon inhibition by complex 3 as compared with 16.9% for reference compound (selegiline). Complexes with bromine ligand show higher activity than those with chlorine ligand. The results of this study can be used in organometallic and bioinorganic chemistry.
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Об авторах
M. Denisov
Institute of Technical Chemistry, Ural Branch
Автор, ответственный за переписку.
Email: denisov.m@itcras.ru
Россия, Perm, 614013
M. Dmitriev
Perm State University
Email: denisov.m@itcras.ru
Россия, Perm, 614990
D. Eroshenko
Institute of Technical Chemistry, Ural Branch
Email: denisov.m@itcras.ru
Россия, Perm, 614013
P. Slepukhin
Ural State Technical University; Postovskii Institute of Organic Synthesis, Ural Branch
Email: denisov.m@itcras.ru
Россия, Yekaterinburg, 620002; Yekaterinburg, 620990
S. Shavkunov
Perm State University
Email: denisov.m@itcras.ru
Россия, Perm, 614990
V. Glushkov
Institute of Technical Chemistry, Ural Branch; Perm State University
Email: denisov.m@itcras.ru
Россия, Perm, 614013; Perm, 614990
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