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Synthesis and detection of a seaborgium carbonyl complex

J. EvenHelmholtz-Institut Mainz, 55099 Mainz, GermanyA. YakushevGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyCh. E. DüllmannGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyHiromitsu HabaRIKEN, Wako, Saitama 351-0198, JapanM. AsaiJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanTetsuya K. SatoJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanH.S. BrandGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyA. Di NittoInstitut für Kernchemie, Johannes Gutenberg-Universität Mainz, 55099 Mainz, GermanyR. EichlerDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, SwitzerlandFenglei FanInstitute of Modern Physics, Chinese Academy of Sciences, 730000 Lanzhou, ChinaW. HartmannGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyM. HuangRIKEN, Wako, Saitama 351-0198, JapanE. JägerGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyD. KajiRIKEN, Wako, Saitama 351-0198, JapanJ. KanayaRIKEN, Wako, Saitama 351-0198, JapanY. KaneyaJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanJ. KhuyagbaatarHelmholtz-Institut Mainz, 55099 Mainz, GermanyB. KindlerGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyJens Volker KratzInstitut für Kernchemie, Johannes Gutenberg-Universität Mainz, 55099 Mainz, GermanyJ. KrierGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyYuki KudouRIKEN, Wako, Saitama 351-0198, JapanN. KurzGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyB. LommelGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanySunao MiyashitaDepartment of Chemistry, Hiroshima University, Kagamiyama, Higashi-Hiroshima 739-8526, JapanK. MorimotoRIKEN, Wako, Saitama 351-0198, JapanKosuke MoritaDepartment of Physics, Kyushu University, Higashi-Ku, Fukuoka, 812-8581, JapanMasashi MurakamiDepartment of Chemistry, Niigata University, Niigata, Niigata 950-2181, JapanY. NagameJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanH. NitscheDepartment of Chemistry, University of California, Berkeley, CA 94720-1460, USAKazuhiro OoeDepartment of Chemistry, Niigata University, Niigata, Niigata 950-2181, JapanZongyi QinInstitute of Modern Physics, Chinese Academy of Sciences, 730000 Lanzhou, ChinaM. SchädelJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanJ. SteinerGSI Helmholtzzentrum für Schwerionenforschung GmbH, 64291 Darmstadt, GermanyT. SumitaRIKEN, Wako, Saitama 351-0198, JapanMirei TakeyamaRIKEN, Wako, Saitama 351-0198, JapanKengo TanakaRIKEN, Wako, Saitama 351-0198, JapanAtsushi ToyoshimaJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanK. TsukadaJapan Atomic Energy Agency, Tokai, Ibaraki 319-1195, JapanΑ. TürlerDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, SwitzerlandI. UsoltsevDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, SwitzerlandY. WakabayashiRIKEN, Wako, Saitama 351-0198, JapanY. WangInstitute of Modern Physics, Chinese Academy of Sciences, 730000 Lanzhou, ChinaN. WiehlHelmholtz-Institut Mainz, 55099 Mainz, GermanyS. YamakiDepartment of Physics, Saitama University, Saitama 338-8570, Japan
2014en
ABI

Аннотация

Experimental investigations of transactinoide elements provide benchmark results for chemical theory and probe the predictive power of trends in the periodic table. So far, in gas-phase chemical reactions, simple inorganic compounds with the transactinoide in its highest oxidation state have been synthesized. Single-atom production rates, short half-lives, and harsh experimental conditions limited the number of experimentally accessible compounds. We applied a gas-phase carbonylation technique previously tested on short-lived molybdenum (Mo) and tungsten (W) isotopes to the preparation of a carbonyl complex of seaborgium, the 106th element. The volatile seaborgium complex showed the same volatility and reactivity with a silicon dioxide surface as those of the hexacarbonyl complexes of the lighter homologs Mo and W. Comparison of the product's adsorption enthalpy with theoretical predictions and data for the lighter congeners supported a Sg(CO)6 formulation.

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