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Mixed-valence hexanuclear CoII,III complex with amidoxime: synthesis, structure, and in vitro biological activity against the non-pathogenic strain of Mycolicibacterium smegmatis
The reaction of cobalt(ɪɪ) chloride with p -Br-benzoyl-β-(piperidin-1-yl)propioamid-oxime (L init ) in methanol leads to the hydrolysis of the ligand at the -OCO- ester bond and the formation of the mixed-valence hexanuclear ionic complex [Co II 2 Co III 4 (HL) 4 (L) 2 (O)-(Cl) 4 ]Cl 2 •4CH 3 OH ( 1...
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Published in: | Russian chemical bulletin 2022-10, Vol.71 (10), p.2172-2178 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The reaction of cobalt(ɪɪ) chloride with
p
-Br-benzoyl-β-(piperidin-1-yl)propioamid-oxime (L
init
) in methanol leads to the hydrolysis of the ligand at the -OCO- ester bond and the formation of the mixed-valence hexanuclear ionic complex [Co
II
2
Co
III
4
(HL)
4
(L)
2
(O)-(Cl)
4
]Cl
2
•4CH
3
OH (
1
) (L is β-(piperidin-l-yl)propioamidoxime). According to the X-ray diffraction data, the ligand (L) in
1
is coordinated to the complexing agent in different modes: the μ
3
-bridging-chelating mode (involving deprotonated amino groups) and the μ
2
- and μ
3
-bridging-chelating modes in the case of a coordinated amino group. Two cobalt atoms of the hexanuclear metal core have a tetrahedral coordination geometry (Co
II
N
2
Cl
2
; CN
Co
II
= 4), whereas the other four cobalt atoms are in an octahedral coordination environment of nitrogen and oxygen atoms forming the polyhedra of composition Co
III
O
3
N
3
and Co
III
O
4
N
2
(CN
Co
III
= 6). The evaluation of the
in vitro
biological activity of
1
against the non-pathogenic (virulent H37Rv model) mycobacterial strain of
Mycolicibacterium smegmatis
showed an increase in the efficiency of complex
1
by more than 4–12 times compared to the previously studied Co
II,III
complexes. |
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ISSN: | 1066-5285 1573-9171 |
DOI: | 10.1007/s11172-022-3643-7 |