Journal
TRANSITION METAL CHEMISTRY
Volume 32, Issue 4, Pages 507-513Publisher
SPRINGER
DOI: 10.1007/s11243-007-0205-7
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Macrocyclic Cu-II stop compounds of the type Cu(L-4)Cl-2 (where L-4 = N-4 or N2O2 donor macrocyclic ligand) have been synthesized by treating the corresponding macrocycles with copper chloride in methanol. These compounds were characterized with the help of elemental analysis, i.r., mass, ESR, electronic spectra, conductance, magnetic and thermal studies. Distorted octahedral geometry has been proposed for all of these compounds. These compounds were found to be efficient in the catalytic oxidation of ascorbic acid and the percentage yields of oxidation products were determined spectrophotometrically. The biological activities of these compounds have been tested against gram +ve and gram -ve bacteria and found to be more active when compared with commercially available antibacterials like streptomycin and ampicillin.
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