TY - JOUR
T1 - Co-precipitation behaviour of single atoms of rutherfordium in basic solutions
AU - Kasamatsu, Yoshitaka
AU - Toyomura, Keigo
AU - Haba, Hiromitsu
AU - Yokokita, Takuya
AU - Shigekawa, Yudai
AU - Kino, Aiko
AU - Yasuda, Yuki
AU - Komori, Yukiko
AU - Kanaya, Jumpei
AU - Huang, Minghui
AU - Murakami, Masashi
AU - Kikunaga, Hidetoshi
AU - Watanabe, Eisuke
AU - Yoshimura, Takashi
AU - Morita, Kosuke
AU - Mitsugashira, Toshiaki
AU - Takamiya, Koichi
AU - Ohtsuki, Tsutomu
AU - Shinohara, Atsushi
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021/3
Y1 - 2021/3
N2 - 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. [Figure not available: see fulltext.]
AB - 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. [Figure not available: see fulltext.]
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U2 - 10.1038/s41557-020-00634-6
DO - 10.1038/s41557-020-00634-6
M3 - Article
C2 - 33589784
AN - SCOPUS:85101458433
SN - 1755-4330
VL - 13
SP - 226
EP - 230
JO - Nature Chemistry
JF - Nature Chemistry
IS - 3
ER -