Gas-Phase Reactivity of Actinides Monocations with NH<sub>3</sub>: ICP-MS Experiments Combined with a DFT Study

The reactivity of actinide monocations (Th<sup>+</sup>, U<sup>+</sup>, Np<sup>+</sup>, Pu<sup>+</sup>, Am<sup>+</sup>, and Cm<sup>+</sup>) with NH<sub>3</sub> gas was studied in the reaction cell of an inductively coupled plasma-mass spectrometer (ICP-MS). Only Th<sup>+</sup>, U<sup>+</sup>, Np<sup>+</sup>, and Cm<sup>+</sup> react completely with NH<sub>3</sub> to form AnNH<sup>+</sup>, contrary to Pu<sup>+</sup> and Am<sup>+</sup>. Differences in reactivity are found between U<sup>+</sup>/Pu<sup>+</sup>, Pu<sup>+</sup>/Cm<sup>+</sup>, and Am<sup>+</sup>/Cm<sup>+</sup>, which could resolve isobaric interferences in ICP-MS. DFT calculations were performed across the first half of the actinide series. The calculated reaction energy between An<sup>+</sup> and NH<sub>3</sub> reproduces the experimental trends in reactivity with Th<sup>+</sup> > Pa<sup>+</sup> > U<sup>+</sup> > Np<sup>+</sup> > Ac<sup>+</sup> > Cm<sup>+</sup> > Pu<sup>+</sup> > Am<sup>+</sup>. The reaction path involves the initial formation of an AnNH<sub>3</sub><sup>+</sup> adduct followed by N-H bond insertion with the formation of HAnNH<sub>2</sub><sup>+</sup> and H<sub>2</sub>AnNH<sup>+</sup> intermediate species and subsequent H<sub>2</sub> loss. The trend in reactivity across the actinides is largely due to the first energy barrier and formation of the HAnNH<sub>2</sub><sup>+</sup> intermediate species. This limiting step is energetically unfavorable for the Pu<sup>+</sup> and Am<sup>+</sup> cations. For these cations, the excitation energy required to achieve a reactive configuration with two non-f electrons available for bonding is too high.

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Journal
Inorganic Chemistry
Published
2024-10-28
DOI
https://doi.org/10.1021/acs.inorgchem.4c03363
Citations
3
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.48
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article

Gas-Phase Reactivity of Actinides Monocations with NH3: ICP-MS Experiments Combined with a DFT Study

Dominique Guillaumont, Alexandre Quémet, Mathilde Goujet
3 citations
Inorganic Chemistry
Radioactive element chemistry and processing
0.48
article

Gas-Phase Reactivity of Actinides Monocations with NH3: ICP-MS Experiments Combined with a DFT Study

Dominique Guillaumont, Alexandre Quémet, Mathilde Goujet
article en
3 citations

Abstract

The reactivity of actinide monocations (Th<sup>+</sup>, U<sup>+</sup>, Np<sup>+</sup>, Pu<sup>+</sup>, Am<sup>+</sup>, and Cm<sup>+</sup>) with NH<sub>3</sub> gas was studied in the reaction cell of an inductively coupled plasma-mass spectrometer (ICP-MS). Only Th<sup>+</sup>, U<sup>+</sup>, Np<sup>+</sup>, and Cm<sup>+</sup> react completely with NH<sub>3</sub> to form AnNH<sup>+</sup>, contrary to Pu<sup>+</sup> and Am<sup>+</sup>. Differences in reactivity are found between U<sup>+</sup>/Pu<sup>+</sup>, Pu<sup>+</sup>/Cm<sup>+</sup>, and Am<sup>+</sup>/Cm<sup>+</sup>, which could resolve isobaric interferences in ICP-MS. DFT calculations were performed across the first half of the actinide series. The calculated reaction energy between An<sup>+</sup> and NH<sub>3</sub> reproduces the experimental trends in reactivity with Th<sup>+</sup> > Pa<sup>+</sup> > U<sup>+</sup> > Np<sup>+</sup> > Ac<sup>+</sup> > Cm<sup>+</sup> > Pu<sup>+</sup> > Am<sup>+</sup>. The reaction path involves the initial formation of an AnNH<sub>3</sub><sup>+</sup> adduct followed by N-H bond insertion with the formation of HAnNH<sub>2</sub><sup>+</sup> and H<sub>2</sub>AnNH<sup>+</sup> intermediate species and subsequent H<sub>2</sub> loss. The trend in reactivity across the actinides is largely due to the first energy barrier and formation of the HAnNH<sub>2</sub><sup>+</sup> intermediate species. This limiting step is energetically unfavorable for the Pu<sup>+</sup> and Am<sup>+</sup> cations. For these cations, the excitation energy required to achieve a reactive configuration with two non-f electrons available for bonding is too high.

Inorganic ChemistryVol. 63(45)
Université de Montpellier (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), CEA Marcoule (FR), Institut des Sciences et technologies pour une Economie Circulaire des énergies bas carbone (FR)
Openalex Percentile: Top 42%
Radioactive element chemistry and processing
0.48
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