The influence of the ratio Cu : L on the lability of copper(I1) complexes with simple ligands of different thermodynamic stabilities (L=EDTA, NTA, cysteine, proline or glycine) was investigated in the range 4 : l-l : 3. Chelex-100 and chitin were used parallel and batch wise, to cause the dissociati
Additional evidence of the operational character of the lability of complexes of copper(II) with simple organic ligands
โ Scribed by M. Teresa; S.D. Vasconcelos; Manuel A.O. Azenha
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 825 KB
- Volume
- 333
- Category
- Article
- ISSN
- 0003-2670
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โฆ Synopsis
A fixed analytical window of observation, 5 pmol I--' free copper and 100 pmol 1 ' total copper, but methods different in nature, operation mode and time scale were applied, in parallel, at pH 6.50 and 16"C, to solutions with copper complexes of very different thermodynamic stabilities. Ethylenediaminetetraacetic acid (EDTA), L-cysteine, L-lysine, L-proline and succinate were used as metal buffers. Chitin (batch and column modes), chelex-100 (column mode) and normal pulse anodic stripping voltammetry (NPASV, -0.3 V deposition potential) were used as techniques. A strategy, based on using the mass of polymer that provided uptake of free copper similar to that taken up by Pseudomonas syringne bacterial cells in absence of ligands. was used for all but NPASV methods. Flame atomic absorption spectrophotometry was used for metal detection. The lability of copper complexes with simple organic ligands showed a strongly operational character. The time scale of the physicochemical method used for the determination of lability was not the only parameter inherent to the method that influenced the extent of copper complex dissociation. The nature of both initial and competing ligands and the operation mode may also condition the speciation results.
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Two electroanalytical techniques, direct potentiometry with a copper ion selective electrode (ISE) and potentiometric stripping analysis (PSA), were used to evaluate the lability of copper-f&k acid complexes (Cu-FA) in 0.5 mol/l sodium perchlorate and in synthetic sea water. The determinations were