1970
DOI: 10.1007/bf02513701
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Determination of traces of bismuth by isotopic exchange reaction in the organic phase

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Cited by 18 publications
(10 citation statements)
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“…2) appears to be retained in solution (56,57); consequently they have lower motilities than their monomeric Tl(III) analogues, enabling mixtures of to be readily separated (65). Dithiocarbamate ligands have thus been used for the separation and extraction of (toxic) Tl(I) from Tl(III), as well as other metal ions (64)(65)(66)(67)(68)(69)(70). The complexes…”
Section: Homoleptic and Mixed Bidentate Ligand Complexesmentioning
confidence: 99%
“…2) appears to be retained in solution (56,57); consequently they have lower motilities than their monomeric Tl(III) analogues, enabling mixtures of to be readily separated (65). Dithiocarbamate ligands have thus been used for the separation and extraction of (toxic) Tl(I) from Tl(III), as well as other metal ions (64)(65)(66)(67)(68)(69)(70). The complexes…”
Section: Homoleptic and Mixed Bidentate Ligand Complexesmentioning
confidence: 99%
“…7). These observed trends of E oc in the presence of thiols can be explained by the replacement of uncharged species HgCI 2 by negatively charged species of mercury-thiol complexes [26,27] within the EDL. Calculating the effective charge of thiols, using the Henderson-Hasselbalch equation (as sum of all charges of ionogenic groups including their signs), indicates that in acetate buffer, GSH has a effective charge equal to À0.933, while for CySH and HCySH this charge is close to zero.…”
Section: Open Circuit Experiments With the Thiols Mixturementioning
confidence: 81%
“…The mercury-ions forms more stable complexes [27] in comparison with copper-ions, thus its presence in solutions which containing thiols and copper-ions, prevents the occurring of the reaction (13) and generate premises for the quantification of thiols by using its catalytic effect on the Cu 2+/0 -system.…”
Section: Cyclic Voltammetry Of Reduced Thiolsmentioning
confidence: 99%
“…For propylmercury(II) chloride, log Ps values are known only for ether and benzene, 9 and for butylmercury(II) chloride and pentylmercury(II) chloride only for ether. 9 We obtained the descriptors listed in Table 7 40 give a number of log Ps values for phenylmercury(II) chloride, and a water to octanol partition coefficient is also available. 9 E was estimated as 1.65 by comparison to aromatic solutes and with V = 1.1132, the total of 26 equations were fitted with S = 1.82, A = 0.17, B = 0.43 and L = 6.841 with SD = 0.094 log units.…”
Section: Mercury(ii) Chloridementioning
confidence: 99%