Cationic—Anionic Pd(II) Complexes with Adamantylimidazolium Cation: Synthesis, Structural Study, and MAO-Inhibiting Activity
- 作者: 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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隶属关系:
- Institute of Technical Chemistry, Ural Branch
- Perm State University
- Ural State Technical University
- Postovskii Institute of Organic Synthesis, Ural Branch
- 期: 卷 64, 编号 1 (2019)
- 页面: 56-67
- 栏目: 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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详细
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.
作者简介
M. Denisov
Institute of Technical Chemistry, Ural Branch
编辑信件的主要联系方式.
Email: denisov.m@itcras.ru
俄罗斯联邦, Perm, 614013
M. Dmitriev
Perm State University
Email: denisov.m@itcras.ru
俄罗斯联邦, Perm, 614990
D. Eroshenko
Institute of Technical Chemistry, Ural Branch
Email: denisov.m@itcras.ru
俄罗斯联邦, Perm, 614013
P. Slepukhin
Ural State Technical University; Postovskii Institute of Organic Synthesis, Ural Branch
Email: denisov.m@itcras.ru
俄罗斯联邦, Yekaterinburg, 620002; Yekaterinburg, 620990
S. Shavkunov
Perm State University
Email: denisov.m@itcras.ru
俄罗斯联邦, Perm, 614990
V. Glushkov
Institute of Technical Chemistry, Ural Branch; Perm State University
Email: denisov.m@itcras.ru
俄罗斯联邦, Perm, 614013; Perm, 614990
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