Utility of Interchangeable Coordination Modes of <i>N</i>,<i>N</i>′-Dialkyl-2,6-pyridinediamide Tridentate Pincer Ligands for Solvent Extraction of Pd(II) and Zr(IV) from High-Level Radioactive Liquid Waste

A new class of ligands, <i>N</i>,<i>N</i>'-dialkyl-2,6-pyridinediamide (DRPDA), has been designed with the specific intention of exhibiting interchangeable diversity in coordination modes, including organometallic interactions, for the purpose of solvent extraction of elements relevant to the proper treatment of high-level radioactive liquid waste (HLLW) generated after nuclear fuel reprocessing. Consequently, DRPDA has been observed to extract Pd(II) and Zr(IV) from HNO<sub>3</sub>(aq) to 1-octanol in nearly quantitative yields when the selected ligand is sufficiently hydrophobic. However, concomitance of some of other HLLW components were also found. The extraction selectivity toward Pd(II) and Zr(IV) was markedly enhanced by employing <i>n</i>-dodecane instead of 1-octanol as evidenced by good distribution ratios (<i>D</i><sub>M</sub>) of Pd(II) (<i>D</i><sub>Pd</sub> = 72.5) and Zr(IV) (<i>D</i><sub>Zr</sub> = 12.9), which is several orders of magnitude greater than <i>D</i><sub>M</sub>'s of other HLLW components (10<sup>-3</sup>-10<sup>-2</sup>), where addition of 20 vol % 1-octanol is still required to accelerate the extraction kinetics. Despite direct contact with the highly acidic aqueous phase, deprotonation from one of the amide NH moieties of DRPDA proceeds to form [Pd(DRPDA<sup>-</sup>)(NO<sub>3</sub>)] as a good extractables in the current biphasic system. This Pd(II) complex with a rather unique asymmetric N<sup>-</sup>^N^O tridentate coordination was characterized by SCXRD, elemental analysis and <sup>1</sup>H NMR, and theoretically corroborated by DFT calculations and NBO analysis. In contrast, DRPDA also interacts with Zr<sup>4+</sup> in different tridentate O^N^O mode without any deprotonation. Based on mechanistic differences in the extraction chemistry we clarified, Pd(II) and Zr(IV) coextracted to the organic phase were recovered stepwise by using appropriate stripping agents such as 1.0 M HCl(aq) and 0.10 M HNO<sub>3</sub>(aq), respectively.

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Publication Details

Journal
Inorganic Chemistry
Published
2024-12-10
DOI
https://doi.org/10.1021/acs.inorgchem.4c03844
Citations
1
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.16

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article

Utility of Interchangeable Coordination Modes of N,N′-Dialkyl-2,6-pyridinediamide Tridentate Pincer Ligands for Solvent Extraction of Pd(II) and Zr(IV) from High-Level Radioactive Liquid Waste

Tomoyuki Takeyama, Koichiro Takao, Satoru Tsushima, Yang Cao et al.
1 citations
Inorganic Chemistry
Radioactive element chemistry and processing
0.16
article

Utility of Interchangeable Coordination Modes of N,N′-Dialkyl-2,6-pyridinediamide Tridentate Pincer Ligands for Solvent Extraction of Pd(II) and Zr(IV) from High-Level Radioactive Liquid Waste

Tomoyuki Takeyama, Koichiro Takao, Satoru Tsushima, Yang Cao, Robert Gericke, Tasuku Orino, Ririka Tashiro
article en
1 citations

Abstract

A new class of ligands, <i>N</i>,<i>N</i>'-dialkyl-2,6-pyridinediamide (DRPDA), has been designed with the specific intention of exhibiting interchangeable diversity in coordination modes, including organometallic interactions, for the purpose of solvent extraction of elements relevant to the proper treatment of high-level radioactive liquid waste (HLLW) generated after nuclear fuel reprocessing. Consequently, DRPDA has been observed to extract Pd(II) and Zr(IV) from HNO<sub>3</sub>(aq) to 1-octanol in nearly quantitative yields when the selected ligand is sufficiently hydrophobic. However, concomitance of some of other HLLW components were also found. The extraction selectivity toward Pd(II) and Zr(IV) was markedly enhanced by employing <i>n</i>-dodecane instead of 1-octanol as evidenced by good distribution ratios (<i>D</i><sub>M</sub>) of Pd(II) (<i>D</i><sub>Pd</sub> = 72.5) and Zr(IV) (<i>D</i><sub>Zr</sub> = 12.9), which is several orders of magnitude greater than <i>D</i><sub>M</sub>'s of other HLLW components (10<sup>-3</sup>-10<sup>-2</sup>), where addition of 20 vol % 1-octanol is still required to accelerate the extraction kinetics. Despite direct contact with the highly acidic aqueous phase, deprotonation from one of the amide NH moieties of DRPDA proceeds to form [Pd(DRPDA<sup>-</sup>)(NO<sub>3</sub>)] as a good extractables in the current biphasic system. This Pd(II) complex with a rather unique asymmetric N<sup>-</sup>^N^O tridentate coordination was characterized by SCXRD, elemental analysis and <sup>1</sup>H NMR, and theoretically corroborated by DFT calculations and NBO analysis. In contrast, DRPDA also interacts with Zr<sup>4+</sup> in different tridentate O^N^O mode without any deprotonation. Based on mechanistic differences in the extraction chemistry we clarified, Pd(II) and Zr(IV) coextracted to the organic phase were recovered stepwise by using appropriate stripping agents such as 1.0 M HCl(aq) and 0.10 M HNO<sub>3</sub>(aq), respectively.

Inorganic ChemistryVol. 63(52)
Helmholtz-Zentrum Dresden-Rossendorf (DE), Institute of Science Tokyo (JP), Sanyo-Onoda City University (JP)
Helmholtz-Zentrum Dresden-Rossendorf, Japan Society for the Promotion of Science, Bundesministerium für Umwelt, Naturschutz, nukleare Sicherheit und Verbraucherschutz
Openalex Percentile: Top 55%
Radioactive element chemistry and processing
0.16
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