Structural Analysis of Curium, Promethium, and Early Lanthanides Using 2,2′:6′,2″-Terpyridine in the Presence of Acid

Trivalent lanthanides and actinides are difficult to separate, often relying on subtle differences in bonding between the 4<i>f</i>- and 5<i>f</i>-orbitals. However, trivalent Cm poses additional complexity owing to its half-filled 5f<sup>7</sup> shell. This configuration causes Cm to have very similar properties to several of the early lanthanides, more specifically, similarly sized Pm. In this study, similarities were probed through isolating an isostructural series between the early lanthanides (La-Eu) and Cm with the oligoamine 2,2':6'2″-terpyridine in the presence of acid. Single-crystal X-ray diffraction studies highlighted the similarities of Pm and Cm under these conditions and further demonstrated the difficulty in separating these elements. Despite the similarities, differences exist between interactions of Pm and Cm with terpyridine in the solid state. Interestingly, Cm appears to be more similar to Sm than to Pm. Furthermore, this study continues to probe the fundamental chemistry of Pm and Cm with respect to slight differences that can be leveraged in their separation from each other.

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Publication Details

Journal
Inorganic Chemistry
Published
2026-03-02
DOI
https://doi.org/10.1021/acs.inorgchem.5c04674
Primary Topic
Lanthanide and Transition Metal Complexes
Type
article
Field-Weighted Citation Impact
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article

Structural Analysis of Curium, Promethium, and Early Lanthanides Using 2,2′:6′,2″-Terpyridine in the Presence of Acid

Megan E. Simms, Alyssa Gaiser, Frankie D. White, Trenton B. Vogt
Inorganic Chemistry
Lanthanide and Transition Metal Complexes
article

Structural Analysis of Curium, Promethium, and Early Lanthanides Using 2,2′:6′,2″-Terpyridine in the Presence of Acid

Megan E. Simms, Alyssa Gaiser, Frankie D. White, Trenton B. Vogt
article en

Abstract

Trivalent lanthanides and actinides are difficult to separate, often relying on subtle differences in bonding between the 4<i>f</i>- and 5<i>f</i>-orbitals. However, trivalent Cm poses additional complexity owing to its half-filled 5f<sup>7</sup> shell. This configuration causes Cm to have very similar properties to several of the early lanthanides, more specifically, similarly sized Pm. In this study, similarities were probed through isolating an isostructural series between the early lanthanides (La-Eu) and Cm with the oligoamine 2,2':6'2″-terpyridine in the presence of acid. Single-crystal X-ray diffraction studies highlighted the similarities of Pm and Cm under these conditions and further demonstrated the difficulty in separating these elements. Despite the similarities, differences exist between interactions of Pm and Cm with terpyridine in the solid state. Interestingly, Cm appears to be more similar to Sm than to Pm. Furthermore, this study continues to probe the fundamental chemistry of Pm and Cm with respect to slight differences that can be leveraged in their separation from each other.

Inorganic ChemistryVol. 65(10)
Oak Ridge National Laboratory (US), Facility for Rare Isotope Beams, Michigan State University (US)
Clean water and sanitation
Openalex Percentile: Top 40%
Lanthanide and Transition Metal Complexes
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