Complex Formation of Ferric Iron with 7-Iodo-8-hydroxyquinoline-5-sulfonic Acid (Ferron).
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Spectrophotometric Determination of Tantalum(V) with 5-Iodo-8- -hydroxyquinoline-7-sulphonic Acid
Tantalum(V) reacts with 5-iodo-8-hydroxyquinoline-7-sulphonic acid to form a yellowish coloured complex having maximum absorbance at 405 nm in citric acid medium. The relatively slow reaction at room temperature is completed in 10 minutes at 40 °c. The colour is stable for at least 12 hr. Effects of heating temperature, time, pH, reagent concentration and other variables have been studied. The ...
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Seventy-eight metal species are examined for fluorescence properties of their chelates with 8-hydroxyquinoline-5-sutfonic acid (HQS); 42 of these fluoresce, many intensely. The optimum pH, determined by ligand ionization vs. hydroxo compiex formation, iles between 5 and 8. Cadmlum forms the most fluorescent complex In a purely aqueous solution. Fluorescence Is enhanced for many metals in surfac...
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The formation and entrapment of tris(8-hydroxyquinoline)aluminum (Alq₃) molecules on the surface of anodic porous alumina (APA) immersed in an ethanol solution of 8-hydroxyquinoline (HQ) were investigated by absorption, fluorescence, and Raman spectroscopies. The effects of the selected APA preparation conditions (galvanostatic or potentiostatic anodization method, anodizing current and voltage...
متن کاملComplex formation reactions of Scandium(III), Yttrium(III) and Lanthanum(III) complexes with 8-Hydroxyquinoline
This study aims to investigate the nature and types of complexes formed in aqueous solution between 8Hydroxyquinoline (HQ) and the ions of Sc, Y, and La. Potentiometric titration was used to follow the formation of complexes. The coordination compounds formed were studied through the determination of stability constants of these complexes in aqueous solution at 25,0 ± 0,1oC and ionic strength o...
متن کامل5-Carboxy-8-hydroxyquinoline is a Broad Spectrum 2-Oxoglutarate Oxygenase Inhibitor which Causes Iron Translocation.
2-Oxoglutarate and iron dependent oxygenases are therapeutic targets for human diseases. Using a representative 2OG oxygenase panel, we compare the inhibitory activities of 5-carboxy-8-hydroxyquinoline (IOX1) and 4-carboxy-8-hydroxyquinoline (4C8HQ) with that of two other commonly used 2OG oxygenase inhibitors, N-oxalylglycine (NOG) and 2,4-pyridinedicarboxylic acid (2,4-PDCA). The results reve...
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ژورنال
عنوان ژورنال: Acta Chemica Scandinavica
سال: 1961
ISSN: 0904-213X
DOI: 10.3891/acta.chem.scand.15-1765