| Literature DB >> 36050378 |
Ian Colliard1,2, Jonathan R I Lee3, Christopher A Colla4, Harris E Mason5,6, April M Sawvel3, Mavrik Zavarin1, May Nyman2, Gauthier J-P Deblonde7,8.
Abstract
The synthesis and study of radioactive compounds are both inherently limited by their toxicity, cost and isotope scarcity. Traditional methods using small inorganic or organic complexes typically require milligrams of sample-per attempt-which for some isotopes is equivalent to the world's annual supply. Here we demonstrate that polyoxometalates (POMs) enable the facile formation, crystallization, handling and detailed characterization of metal-ligand complexes from microgram quantities owing to their high molecular weight and controllable solubility properties. Three curium-POM complexes were prepared, using just 1-10 μg per synthesis of the rare isotope 248Cm3+, and characterized by single-crystal X-ray diffraction, showing an eight-coordinated Cm3+ centre. Moreover, spectrophotometric, fluorescence, NMR and Raman analyses of several f-block element-POM complexes, including 243Am3+ and 248Cm3+, showed otherwise unnoticeable differences between their solution versus solid-state chemistry, and actinide versus lanthanide behaviour. This POM-driven strategy represents a viable path to isolate even rarer complexes, notably with actinium or transcalifornium elements.Entities:
Year: 2022 PMID: 36050378 DOI: 10.1038/s41557-022-01018-8
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274