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Stability Series for the Complexation of Six Key Siderophore Functional Groups with Uranyl Using Density Functional Theory.

Authors :
Kirby ME
Sonnenberg JL
Simperler A
Weiss DJ
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