Synthesis, characterization, and antimicrobial studies of some palladium complexes with an octamethyl tetraazacyclotetradecadiene ligand and isomers of its reduced form
Biologically important tetraaza-macrocyclic ligand 3,10-C-meso-3,5,7,7,10,12,14,14-octamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene dihydroperchlorate, Me 8 [14]diene·2HClO 4 (L 1 ·2HClO 4 ) was synthesized by the condensation of 1,2-diaminopropane with acetone in presence of quantitative amoun...
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Published in | Journal of the Iranian Chemical Society Vol. 15; no. 9; pp. 1947 - 1959 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.09.2018
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Biologically important tetraaza-macrocyclic ligand 3,10-C-meso-3,5,7,7,10,12,14,14-octamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene dihydroperchlorate, Me
8
[14]diene·2HClO
4
(L
1
·2HClO
4
) was synthesized by the condensation of 1,2-diaminopropane with acetone in presence of quantitative amount of HClO
4
and three isomeric ligands designated as L
A
, L
B
and L
C
were separated by the reduction of L
1
·2HClO
4
with NaBH
4
and fractional crystallization from xylene. The nitrato, nitro, bromido, and iodido complexes of palladium with diene ligand L
1
were prepared by the interaction of L
1
·2HClO
4
with K
2
[Pd(NO
3
)
4
], K
2
[Pd(NO
2
)
4
], K
2
[PdBr
4
], and K
2
[PdI
4
] (prepared by the reactions with PdCl
2
with KNO
3
, KNO
2
, KBr, and KI, respectively), respectively. The bromide and iodido complexes of L
A
were prepared by the axial substitution reactions with [PdL
A
Cl
2
]Cl
2
. By contrast, similar complexes of other isomeric ligands L
B
and L
C
were prepared by axial addition reactions of [PdL
ʹ
][PdCl
4
] (L′ = L
B
or L
C
) with KBr and KI, respectively. The complexes were characterized on the basis of elemental analysis: IR,
1
H-NMR, UV–Vis spectroscopic analysis, and magnetic and molar conductivity data. The antifungal and antibacterial activities of these compounds have been studied against some phyto-pathogenic fungi and bacteria. |
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ISSN: | 1735-207X 1735-2428 |
DOI: | 10.1007/s13738-018-1392-1 |