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1.
Chem Biodivers ; 21(5): e202301667, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38502834

RESUMEN

In this paper, a new tridentate Schiff base ligand (L) with nitrogen donor atoms and its cadmium(II) complexes with the general formula of CdLX2 (X=Cl-, Br-, I-, SCN-, N3 -, NO3 -) have been synthesized and characterized by physical and spectral (FT/IR, UV-Vis, Mass, and 1H, 13C NMR spectroscopies) methods. Also nano-structured cadmium chloride and bromide complexes were synthesized by sonochemical method and then used to prepare nanostructured cadmium oxide confirmed by XRD and SEM techniques. Thermal behavior of the compounds was studied in the temperature range of 25 to 900 °C under N2 atmosphere at a heating rate of 20 °C/ min. Moreover, thermo-kinetic activation parameters of thermal decomposition steps were calculated according to the Coats-Redfern relationship. Antimicrobial activities of the synthesized compounds against two gram-positive and two gram-negative bacteria such as Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and two fungi of Candida albicans and Aspergillus niger were investigated by well diffusion method. SEM technique was used to monitor the morphological changes of the bacteria treated with the compounds. The 2,2-Diphenyl-1-picrylhydrazyl(DPPH) and the ferric reducing antioxidant power (FRAP) methods were used to evaluate the antioxidant ability of the ligand and its cadmium(II) complexes. In final, the cytotoxicity properties of the ligand and some cadmium(II) complexes against PC3 cancer cells were evaluated by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide) bioassay and nitric oxide (NO) level measurement. The morphological changes of prostate cancer (PC3) cells due to treatment with the ligand and its complexes confirmed their anticancer effectiveness.


Asunto(s)
Antineoplásicos , Antioxidantes , Cadmio , Complejos de Coordinación , Pruebas de Sensibilidad Microbiana , Antioxidantes/farmacología , Antioxidantes/síntesis química , Antioxidantes/química , Humanos , Antineoplásicos/farmacología , Antineoplásicos/síntesis química , Antineoplásicos/química , Cadmio/química , Cadmio/farmacología , Complejos de Coordinación/farmacología , Complejos de Coordinación/química , Complejos de Coordinación/síntesis química , Antibacterianos/farmacología , Antibacterianos/síntesis química , Antibacterianos/química , Antifúngicos/farmacología , Antifúngicos/síntesis química , Antifúngicos/química , Línea Celular Tumoral , Ensayos de Selección de Medicamentos Antitumorales , Bacterias Grampositivas/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Bacterias Gramnegativas/efectos de los fármacos , Estructura Molecular , Bases de Schiff/química , Bases de Schiff/farmacología , Bases de Schiff/síntesis química , Compuestos de Bifenilo/antagonistas & inhibidores , Compuestos de Bifenilo/química , Compuestos de Bifenilo/farmacología , Candida albicans/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Hongos/efectos de los fármacos , Relación Estructura-Actividad , Picratos/antagonistas & inhibidores , Antiinfecciosos/farmacología , Antiinfecciosos/síntesis química , Antiinfecciosos/química , Temperatura
2.
Mater Sci Eng C Mater Biol Appl ; 61: 809-23, 2016 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-26838912

RESUMEN

Some new five coordinated ZnLX2 complexes, where L is N3-Schiff base ligand obtained by condensation reaction between diethylenetriamine and (E)-3-(2-nitrophenyl)acrylaldehyde and X (Cl(-), Br(-), I(-), N3(-) and NCS(-)), were synthesized and characterized by FT-IR, (1)H and (13)CNMR, UV-visible, ESI-mass spectra and molar conductivity measurements. The structures of zinc iodide and thiocyanate complexes were determined by X-ray crystallographic analysis. The X-ray results showed that the Zn (II) center in these complexes is five-coordinated in a distorted trigonal-bipyramidal configuration. Zinc iodide and thiocyanate complexes crystallize in the monoclinic and triclinic systems with space groups of C2/c and P1- with eight and two molecules per unit cell respectively. The crystal packing of the complexes consists of intermolecular interactions such as C-H(…)O and C-H(…)I, C-H(···)S, N(…)O, together with π-π stacking and some other unexpected interactions. The mentioned interactions cause three-dimensional supramolecular structure in the solid state. Zinc complexes were also prepared in nano-structure by sonochemical method confirmed by XRD, SEM and TEM analyses. Moreover, ZnO nanoparticles were synthesized by direct thermolysis of zinc iodide complex. Furthermore, antimicrobial and thermal properties of the compounds were completely investigated.


Asunto(s)
Antiinfecciosos/síntesis química , Complejos de Coordinación/síntesis química , Zinc/química , Antiinfecciosos/química , Antiinfecciosos/farmacología , Aspergillus oryzae/efectos de los fármacos , Candida albicans/efectos de los fármacos , Complejos de Coordinación/química , Complejos de Coordinación/farmacología , Cristalografía por Rayos X , Bacterias Gramnegativas/efectos de los fármacos , Bacterias Grampositivas/efectos de los fármacos , Enlace de Hidrógeno , Ligandos , Espectroscopía de Resonancia Magnética , Nanopartículas del Metal/química , Conformación Molecular , Bases de Schiff/química , Espectroscopía Infrarroja por Transformada de Fourier
3.
Mater Sci Eng C Mater Biol Appl ; 55: 462-70, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26117778

RESUMEN

Some new cadmium(II) Schiff base complexes CdLX2 (where X=Cl(-), Br(-), I(-), SCN(-) and N3(-) and L=N,N-bis((E)-3-(4-(dimethylamino)phenyl)allylidene)benzene-1,2-diamine) were synthesized and characterized by elemental analysis, FT-IR, UV-visible, (1)HNMR spectra, and conductivity measurements. Moreover, the structure of the CdLI2 was determined by single crystal X-ray crystallography. CdLI2 crystallizes in a triclinic system with space group P 1̅. The molecular structure shows distorted tetrahedral coordination geometry. The CH....π and π-π stacking interactions connect the molecules to a supramolecular network. The thermal properties of the compounds were investigated from the room temperature to 800 °C with a heating rate of 10 °C/min and decomposition activation parameters were evaluated from the TG/DTG plots. Antibacterial/antifungal activities of the compounds were screened by the disk diffusion method against the Gram-negative bacteria Escherichia coli and Pseudomonas aeruginosa, the Gram-positive bacteria Staphylococcus aureus and Bacillus subtilis and the fungi strain Aspergillus niger and Candida albicans. The antimicrobial activities were determined for all compounds and the complexation was found to enhance the inhibitory activity. Finally, the DNA cleavage potential of the compounds was investigated by agarose gel electrophoresis method.


Asunto(s)
Antiinfecciosos/farmacología , ADN/efectos de los fármacos , Bases de Schiff/química , Cristalografía por Rayos X , Hidrólisis , Pruebas de Sensibilidad Microbiana , Espectroscopía de Protones por Resonancia Magnética
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