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

氢氧化物 化学 Atom(片上系统) 离子 降水 吸附 锕系元素 无机化学 物理化学 有机化学 物理 气象学 计算机科学 嵌入式系统
作者
Y. Kasamatsu,Keigo Toyomura,Hiromitsu Haba,Takuya Yokokita,Yudai Shigekawa,Aiko Kino,Yuki Yasuda,Yukiko Komori,J. Kanaya,Minghui Huang,Masashi Murakami,H. Kikunaga,Eisuke Watanabe,Takashi Yoshimura,Kosuke Morita,T. Mitsugashira,Koichi Takamiya,T. Ohtsuki,Atsushi Shinohara
出处
期刊:Nature Chemistry [Springer Nature]
卷期号:13 (3): 226-230 被引量:13
标识
DOI:10.1038/s41557-020-00634-6
摘要

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. 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.
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