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Stability Series for the Complexation of Six Key Siderophore Functional Groups with Uranyl Using Density Functional Theory.
- Source :
-
The journal of physical chemistry. A [J Phys Chem A] 2020 Mar 26; Vol. 124 (12), pp. 2460-2472. Date of Electronic Publication: 2020 Mar 16. - Publication Year :
- 2020
-
Abstract
- Determining stability constants of uranyl complexes with the principal functional groups in siderophores and identifying stability series is of great importance to predict which siderophore classes preferentially bind to U <superscript>VI</superscript> and, hence, impact uranium speciation in the environment. It also helps to develop resins for scavenging U <superscript>VI</superscript> from aqueous solutions. Here, we apply a recently developed computational approach to calculate log β values for a set of geochemically relevant uranium organometallic complexes using Density Functional Theory (DFT). We determined the stability series for catecholate, hydroxamate, α-hydroxycarboxylate, α-aminocarboxylate, hydroxy-phenyloxazolonate, and α-hydroxyimidazole with the uranyl cation. In this work, the stability constants (log β <subscript>110</subscript> ) of α-hydroxyimidazolate and hydroxy-phenyloxazolonate are calculated for the first time. Our approach employed the B3LYP density functional approximation, aug-cc-pVDZ basis set for ligand atoms, MDF60 ECP for U <superscript>VI</superscript> , and the IEFPCM solvation model. DFT calculated log β <subscript>110</subscript> were corrected using a previously established fitting equation. We find that the siderophore functional groups stability decreases in the order: α-hydroxycarboxylate bound via the α-hydroxy and carboxylate groups (log β <subscript>110</subscript> = 17.08), α-hydroxyimidazolate (log β <subscript>110</subscript> = 16.55), catecholate (log β <subscript>110</subscript> = 16.43), hydroxamate (log β <subscript>110</subscript> = 9.00), hydroxy-phenyloxazolonate (log β <subscript>110</subscript> = 8.43), α-hydroxycarboxylate bound via the carboxylate group (log β <subscript>110</subscript> = 7.51) and α-aminocarboxylate (log β <subscript>110</subscript> = 4.73). We confirm that the stability for the binding mode of the functional groups decrease in the order: bidentate, monodentate via ligand O atoms, and monodentate via ligand N atoms. The stability series strongly suggests that α-hydroxyimidazolate is an important functional group that needs to be included when assessing uranyl mobility and removal from aqueous solutions.
Details
- Language :
- English
- ISSN :
- 1520-5215
- Volume :
- 124
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- The journal of physical chemistry. A
- Publication Type :
- Academic Journal
- Accession number :
- 32092265
- Full Text :
- https://doi.org/10.1021/acs.jpca.9b10649