2014
DOI: 10.1016/j.jiec.2013.10.027
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Some new cadmium complexes: Antibacterial/antifungal activity and thermal behavior

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Cited by 50 publications
(34 citation statements)
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“…[33] As a sequence of iminic nitrogen participation in binding to mercury ion and the formation of complexes, the first band was shifted to lower wavelengths by 13 nm while the second one (intensive absorption) had extremely red shifted to 364-415 nm. Furthermore, the electronic spectrum of HgLBr 2 exhibited another absorption peak at 467 nm that can be related to metal to ligand charge transfer (MLCT) transition.…”
Section: Uv-visible Spectramentioning
confidence: 99%
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“…[33] As a sequence of iminic nitrogen participation in binding to mercury ion and the formation of complexes, the first band was shifted to lower wavelengths by 13 nm while the second one (intensive absorption) had extremely red shifted to 364-415 nm. Furthermore, the electronic spectrum of HgLBr 2 exhibited another absorption peak at 467 nm that can be related to metal to ligand charge transfer (MLCT) transition.…”
Section: Uv-visible Spectramentioning
confidence: 99%
“…The Schiff base ligand of bis(3-(4-dimethylaminophenyl)-2-prop-1-enylydene)-1,2-diaminoethane was prepared from condensation reaction of ethylene diamine (0.5 mmol, 0.03 g) and 4-dimethylaminophenylpropenal (1 mmol, 0.175 g) in ethanol solvent under rigorous stirring for 5 h. [33] At the end of reaction, the ligand orange precipitate was separated. For more purification of product, it was washed twice with ethanol and then recrystallized from mixture of ethanol/dichloromethane solvents (1:1) to yield the orange crystalline powder in 54%.…”
Section: Synthesis Of Ligand (L)mentioning
confidence: 99%
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“…In-vitro biological activity of the extracts against two Gram negative bacteria such as Escherichia coli (ATCC 25922) and Pseudomonas aeroginosa (ATCC 9027) and Gram-positive bacteria including S. Bacillus subtilis (ATCC: 6633) and also a fungal strain such as A. oryzae, were carried out using the disk diffusion method [30,31]. For this mean, the Petri dishes were prepared as follows: i) a layer of culture medium (Muller Hinton Agar (Merck, Germany) for bacterial strains and Sabouraud dextrose agar (SDA) for fungal strains was poured on the surface of plates, ii) 100 μl of spore suspension of bacteria and/or fungi including nearly 0.5 × 106 colony-forming units (CFU/ml) was inoculated on the surface of culture medium, iii) The prepared discs (that had been soaked in the various concentrations of Extracts; 12.5, 25 and 50 mg/ml in physiological saline) were placed at different positions on a surface of plates.…”
Section: Biological Activitymentioning
confidence: 99%