Glutarimidedioxime Complexation: Extraction of Uranium vs. Interference of Vanadium and Molybdenum in Seawater

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Inorg. Chem. Front., 2026, Accepted ManuscriptDOI: 10.1039/D6QI00428H, Review ArticleRunwu Li Li, Wei Ding, Bijun Liu, Xingliang LiThe cyclic imide dioxime ligand, glutarimidedioxime (H3A), has emerged as a paradigm-shifting archetype in chemistry of coordina…

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Glutarimidedioxime Complexation: Extraction of Uranium vs. Interference of Vanadium and Molybdenum in Seawater

Abstract

The cyclic imide dioxime ligand, glutarimidedioxime (H3A), has emerged as a paradigm-shifting archetype in chemistry of coordination and separation. Its prominence is driven by the formidable challenge of extracting ultra trace uranium from seawater, a critical endeavor for sustainable nuclear energy. This review provides a comprehensive and critical synthesis of research that positions H3A as the definitive active motif in advanced amidoxime-based sorbents. We first delineate its structural elucidation, optimal synthesis, and its distinctive acid-base properties. A higher temperature (80~90 °C) promotes intramolecular cyclization of two adjacent nitrile groups and favors the synthesis of H3A, while avoiding excess hydroxylamine to prevent formation of glutarimidoxioxime. The core analysis presents a comparative examination of its coordination chemistry, governed by a hierarchy of ionic potential. H3A contains a conjugated system that forms very stable complexes with the uranyl ion. In the complex, H3A coordinates with the uranyl ion through a tridentate chelation pocket. This strong coordination enables it to compete with carbonate for the uranyl ion even at ultra-low concentrations. A central focus is the ligand’s exceptional ability to displace oxo ligands from vanadate, forming an ultra-stable, rare non-oxido V(V) complex [V(A)2]⁻, which defines the severe vanadium interference problem. Furthermore, we critically examine the previously overlooked but critical interaction with molybdenum, which catalyzes the hydrolytic degradation of the H3A motif and poses a fundamental threat to long-term sorbent viability. By integrating molecular-scale insights with macroscopic application performance, this review clarifies the intricate structure-property relationships responsible for both the promise and limitations of H3A-based technology. Finally, we chart a course for future research, emphasizing ligand design strategies to decouple uranyl from vanadium affinity and to mitigate degradation pathways, thereby guiding the development of next-generation functional materials for resource recovery and separations science.

• This article is part of the themed collections: 2026 Inorganic Chemistry Frontiers HOT Articles and 2026 Inorganic Chemistry Frontiers Review-type Articles