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Copper(II) complexes with phenoxyalkanoic acids and nitrogen donor heterocyclic ligands: structure and bioactivity.
- Source :
-
Journal of inorganic biochemistry [J Inorg Biochem] 2001 Jan 01; Vol. 83 (1), pp. 7-16. - Publication Year :
- 2001
-
Abstract
- The copper complexes with the phenoxyalkanoic acids MCPA, 2,4-D, 2,4,5-T and 2,4-DP in the presence of a nitrogen donor heterocyclic ligand, phen or bipyam, were prepared and characterized. Interaction of Cu(II) with phenoxyalkanoic acids and bipyam leads to dinuclear or uninuclear neutral complexes while in the presence of phen uninuclear neutral or cationic forms have been isolated. The crystal structure of bis(1,10-phenanthroline)(2-methyl-4-chloro-phenoxyacetato)copper(ll) chloride-methanol(1/1)-water(1/0.6), 1 has been determined and refined by least-squares methods using three-dimensional MoK, data. 1 crystallizes in space group P1, in a cell of dimensions a = 14.577(6)A, b = 1 1.665(5) A, c = 12.249(6) A, alpha = 98.38( 1)degrees, beta = 112.18( 1) degrees, gamma = 104.56(1 ) degrees, V= 1,798( 1) A3 and Z= 2. The cyclic voltammograms of uninuclear cationic complexes in dmf exhibit an extra cathodic wave due to the chloride ion. The available evidence supports an increasing antimicrobial effeciency for the cationic complexes.
- Subjects :
- Anti-Bacterial Agents chemistry
Anti-Bacterial Agents pharmacology
Bacteria drug effects
Carboxylic Acids chemical synthesis
Carboxylic Acids pharmacology
Crystallography, X-Ray
Electrochemistry
Heterocyclic Compounds pharmacology
Ligands
Microbial Sensitivity Tests
Models, Molecular
Molecular Structure
Nitric Oxide Donors metabolism
Nitric Oxide Donors pharmacology
Spectrum Analysis
Structure-Activity Relationship
Carboxylic Acids chemistry
Copper chemistry
Heterocyclic Compounds chemistry
Nitric Oxide Donors chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0162-0134
- Volume :
- 83
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of inorganic biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 11192702
- Full Text :
- https://doi.org/10.1016/s0162-0134(00)00131-8