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

Read full text
Authors: Trenton Vogt, Megan E. Simms, Alyssa Gaiser, Frankie D. White
Cited by: 1
References: 43

Abstract

High Resolution Image Download MS PowerPoint Slide Trivalent lanthanides and actinides are difficult to separate, often relying on subtle differences in bonding between the 4 f – and 5 f –orbitals. However, trivalent Cm poses additional complexity owing to its half-filled 5f 7 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.

Fields of Study & Subjects

Lanthanide and Transition Metal Complexes Organometallic Complex Synthesis and Catalysis Coordination Chemistry and Organometallics

Publication details

Journal / source
Inorganic Chemistry
Publisher
American Chemical Society (ACS)
Volume
65
Issue
10
Pages
5299–5305
Publication date
2 March 2026
Language
EN