2014
DOI: 10.1039/c4dt02757d
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Speciation and the structure of lead(ii) in hyper-alkaline aqueous solution

Abstract: In hyper-alkaline aqueous solutions, lead(ii) is present exclusively as [Pb(OH)3]−. Other species, like [Pb(OH)4]2−, [PbOOH]−or [PbO2]2−are not detectable.

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Cited by 12 publications
(6 citation statements)
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“…At alkaline pH, dissociation of thiols favors thiolates, which could lead to increased quenching. However, the alkaline condition would cause the formation of lead hydroxides such as [Pb­(OH)] + , Pb­(OH) 2 , and complexes that reduce the availability of free Pb 2+ to quench the fluorescence of the HS-C/Au(1.4)/UiO-66 film. At the acidic pH, thiolate formation from the dissociation of the −SH group is not favored, hence the quenching response of the HS-C/Au(1.4)/UiO-66 film is lower than at pH 7.…”
Section: Resultsmentioning
confidence: 99%
“…At alkaline pH, dissociation of thiols favors thiolates, which could lead to increased quenching. However, the alkaline condition would cause the formation of lead hydroxides such as [Pb­(OH)] + , Pb­(OH) 2 , and complexes that reduce the availability of free Pb 2+ to quench the fluorescence of the HS-C/Au(1.4)/UiO-66 film. At the acidic pH, thiolate formation from the dissociation of the −SH group is not favored, hence the quenching response of the HS-C/Au(1.4)/UiO-66 film is lower than at pH 7.…”
Section: Resultsmentioning
confidence: 99%
“…The coordination chemistry of tin(II) and lead(II) is strongly affected by occupied anti-bonding orbitals causing large voids, so-called gaps, in their coordination spheres. [3][4][5][6] This is not the case for the tetravalent ions, but for neither tin(IV) nor lead(IV), no hydrate or solvate structures have previously been reported. We have made several attempts to prepare aqueous solutions of hydrated tin(IV) ions in strongly acidic solution, but it always resulted in precipitation of solid tin(IV) oxide, SnO 2 .…”
Section: Introductionmentioning
confidence: 89%
“…hyd./sol. 1.957 [11] 2.130 [9] 2.229 [5] n/a n/a n/a Tables S4 and S5 OH − 1.973 [7] 2.160 [2] 2.257 [1] 1.905 [5] 2.049 [20] 2.158 [4] Tables S1, S4 and S5 r M n+ 0.617 0.790 0.889 n/a n/a n/a 24 r M n+ Sh.…”
Section: Comparison With Other High-valent D 10 Metal Ionsmentioning
confidence: 99%
“…Chromium(III) is adsorbed as hydrolysed tetrameric complexes at both acidic and basic pH values, one chromium in the hydrolyzed tetramer binds to the surface through two oxygens to one or two Fe 3+ ions in the mineral surface. aqueous solution (Bajnóczi et al, 2014). Copper(III) is hydrolyzed to a polymeric complex or precipitateadsorbed to the clay surface.…”
Section: Resultsmentioning
confidence: 99%