Co-precipitation behaviour of single atoms of rutherfordium in basic solutions

It is difficult to investigate the chemical properties of superheavy elements, which are only available an atom at a time and rapidly decay. A co-precipitation method with samarium has now been developed that suggests rutherfordium would form hydroxide precipitates-but not ammine ones-if it were possible to perform these experiments on macroscopic quantities. All superheavy elements (SHEs), with atomic numbers (Z) >= 104, have been artificially synthesized one atom at a time and their chemical properties are largely unknown. Because these heavy nuclei have short lifetimes as well as extremely low production rates, chemical experiments need to be carried out on single atoms and have mostly been limited to adsorption and extraction. We have now investigated the precipitation properties of the SHE Rf (Z = 104). A co-precipitation method with samarium hydroxide had previously established that the co-precipitation behaviour of a range of elements reflected these elements' tendency to form hydroxide precipitates and/or ammine complex ions. Here we investigated co-precipitation of Rf in basic solutions containing NH3 or NaOH. Comparisons between the behaviour of Rf with that of Zr and Hf (lighter homologues of Rf) and actinide Th (a pseudo-homologue of Rf) showed that Rf does not coordinate strongly with NH3, but forms a hydroxide (co)precipitate that is expected to be Rf(OH)(4).

Automated summary

Investigating the chemical properties of superheavy elements, which are only available an atom at a time, is challenging. Researchers have developed a co-precipitation method with samarium to study the precipitation properties of the superheavy element Rf, suggesting it forms hydroxide precipitates.