Abstract:We present the first experimental evidence for the ternary complexation of calcium and magnesium ions with plutonyl(VI) tricarbonate species in carbonate-containing aqueous solutions using visible-NIR spectrophotometric titration. Prior to studying...
“…Only one spectroscopic study of the Pu( vi )-oxalate system has been reported, 20 so additional guidance for understanding changes in our systems was obtained from previous reports on the spectral impact of changing Pu( vi ) coordination. 39–45…”
Section: Discussionmentioning
confidence: 99%
“…Only one spectroscopic study of the Pu(VI)-oxalate system has been reported, 20 so additional guidance for understanding changes in our systems was obtained from previous reports on the spectral impact of changing Pu(VI) coordination. [39][40][41][42][43][44][45] The peaks at 839 and 846 nm were determined to represent Pu(VI)-oxalate complexes that shared the pentagonal bipyramidal coordination environment of the fully hydrated Pu(VI)-aquo ion ([PuO 2 (H 2 O) 6 ] 2+ ). 47 The strong peaks in the 830-850 nm region were lost as the f-f transition became Laporte forbidden with the addition of an inversion center (i.e., hexagonal bipyramidal coordination).…”
Two aqueous Pu(vi)-oxalate species were identified through a spectroscopic study of the Pu(vi)-oxalate system as a function of [oxalate], pH, and metal-to-ligand ratio. The formation constants for both species were calculated from this data.
“…Only one spectroscopic study of the Pu( vi )-oxalate system has been reported, 20 so additional guidance for understanding changes in our systems was obtained from previous reports on the spectral impact of changing Pu( vi ) coordination. 39–45…”
Section: Discussionmentioning
confidence: 99%
“…Only one spectroscopic study of the Pu(VI)-oxalate system has been reported, 20 so additional guidance for understanding changes in our systems was obtained from previous reports on the spectral impact of changing Pu(VI) coordination. [39][40][41][42][43][44][45] The peaks at 839 and 846 nm were determined to represent Pu(VI)-oxalate complexes that shared the pentagonal bipyramidal coordination environment of the fully hydrated Pu(VI)-aquo ion ([PuO 2 (H 2 O) 6 ] 2+ ). 47 The strong peaks in the 830-850 nm region were lost as the f-f transition became Laporte forbidden with the addition of an inversion center (i.e., hexagonal bipyramidal coordination).…”
Two aqueous Pu(vi)-oxalate species were identified through a spectroscopic study of the Pu(vi)-oxalate system as a function of [oxalate], pH, and metal-to-ligand ratio. The formation constants for both species were calculated from this data.
The formation constants of CanUO2(CO3)3(4–2n)– complexes have been determined directly using capillary electrophoresis coupled with inductively coupled plasma mass spectrometry (CE-ICP-MS) in 0.1 M NaCl and at room temperature. Instead...
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