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Multi-nucleon transfer channels of the reactions of 18O+232Th, 18O+238U, 18O+248Cm were used to measure fission-fragment mass distribution for various nuclides and their excitation energy dependence. Predominantly asymmetric fission is observed at low excitation energies for all the studied cases, with an increase of the symmetric fission towards high excitation energies. Experimental data are compared with predictions of the fluctuation-dissipation model, where effects of multi-chance fission (neutron evaporation prior to fission) was introduced. It was shown that a reliable understanding of the observed fission fragment mass distributions can be obtained only invoking multi-chance fissions.

It is shown that multi-nucleon transfer reaction is a powerful tool to study fission of exotic neutronrich actinide nuclei, which cannot be accessed by particle-capture or heavy-ion fusion reactions. In this work, multi-nucleon transfer channels of the reactions of 18O+232Th, 18O+238U, 18O+248Cm, and 18O+237Np were used to measure fission-fragment mass distribution for each transfer channel. Predominantly asymmetric fission is observed at low excitation energies for all the studied cases, with an increase of the symmetric fission towards high excitation energies. Experimental data are compared with predictions of the fluctuation-dissipation model, where effects of multi-chance fission (neutron evaporation prior to fission) was introduced. It is shown that mass-asymmetric structure remaining at high excitation energies originates from low-excited and less neutronrich excited nuclei due to higher-order chance fissions.

The first ionization potential (IP1) of element 103, lawrencium (Lr), has been successfully determined for the first time by using a newly developed method based on a surface ionization process. The measured IP1 value is 4.9630.080.07 eV. This value is the smallest among those of actinide elements and is in excellent agreement with the value of 4.963(15) eV predicted by state-of-the-art relativistic calculations also performed in this work. Our results strongly support that the Lr atom has an electronic configuration of [Rn]7s25f147p11/2, which is influenced by strong relativistic effects. The present work provides a reliable benchmark for theoretical calculations and also opens the way for studies on atomic properties of heavy elements with atomic number Z > 100. Moreover, the present achievement has triggered a controversy on the position of lutetium (Lu) and Lr in the Periodic Table of Elements.

In 2014 the first synthesis of a transactinide carbonyl complex – seaborgium hexacarbonyl – was reported. This was achieved in gas-phase chemical experiments in a beam-free environment behind the recoil separator GARIS. Extending this work to heavier elements requires more efficient techniques to synthesize carbonyl complexes as production rates of transactinide elements drop with increasing atomic number. A novel approach was thus conceived, which retains the benefit of a beam-free environment but avoids the physical preseparation step. The latter reduces the yields for products of asymmetric reactions such as those used for the synthesis of suitable isotopes of Sg, Bh, Hs and Mt. For this a series of experiments with accelerator-produced radioisotopes of the lighter homologues W, Re and Os was carried out at the tandem accelerator of JAEA Tokai, Japan. A newly developed double-chamber system, which allows for a decoupled recoil ion thermalization and chemical complex formation, was used, which avoids the low-efficiency physical preseparation step. Here, we demonstrate the feasibility of this newly developed method using accelerator-produced short-lived radioisotopes of the 5d homologues of the early transactinides. [ABSTRACT FROM AUTHOR]

The formation and the chemical characterization of single atoms of dubnium (Db, element 105), in the form of its volatile oxychloride, was investigated using the on‐line gas phase chromatography technique, in the temperature range 350–600 °C. Under the exactly same chemical conditions, comparative studies with the lighter homologues of Group 5 in the Periodic Table clearly indicate the volatility sequence being NbOCl3 > TaOCl3 ≥ DbOCl3. From the obtained experimental results, thermochemical data for DbOCl3 were derived. The present study delivers reliable experimental information for theoretical calculations on chemical properties of transactinides. [ABSTRACT FROM AUTHOR]

The formation and the chemical characterization of single atoms of dubnium (Db, element 105), in the form of its volatile oxychloride, was investigated using the on‐line gas phase chromatography technique, in the temperature range 350–600 °C. Under the exactly same chemical conditions, comparative studies with the lighter homologues of Group 5 in the Periodic Table clearly indicate the volatility sequence being NbOCl3 > TaOCl3 ≥ DbOCl3. From the obtained experimental results, thermochemical data for DbOCl3 were derived. The present study delivers reliable experimental information for theoretical calculations on chemical properties of transactinides. [ABSTRACT FROM AUTHOR]

The formation and the chemical characterization of single atoms of dubnium (Db, element 105), in the form of its volatile oxychloride, was investigated using the on‐line gas phase chromatography technique, in the temperature range 350–600 °C. Under the exactly same chemical conditions, comparative studies with the lighter homologues of Group 5 in the Periodic Table clearly indicate the volatility sequence being NbOCl3 > TaOCl3 ≥ DbOCl3. From the obtained experimental results, thermochemical data for DbOCl3 were derived. The present study delivers reliable experimental information for theoretical calculations on chemical properties of transactinides. [ABSTRACT FROM AUTHOR]

The formation and the chemical characterization of single atoms of dubnium (Db, element 105), in the form of its volatile oxychloride, was investigated using the on‐line gas phase chromatography technique, in the temperature range 350–600 °C. Under the exactly same chemical conditions, comparative studies with the lighter homologues of Group 5 in the Periodic Table clearly indicate the volatility sequence being NbOCl3 > TaOCl3 ≥ DbOCl3. From the obtained experimental results, thermochemical data for DbOCl3 were derived. The present study delivers reliable experimental information for theoretical calculations on chemical properties of transactinides. [ABSTRACT FROM AUTHOR]

We have studied extraction behavior of group-6 elements Mo and W to search for suitable conditions for an on-line extraction experiment of their heavier homolog, seaborgium (Sg). Batch-wise extraction of carrier-free radiotracers 93mMo and 177,179,181W were carried out from 0.10 - 8.6 M H2SO4 and 1.0 × 10−4 − 5.0 M HF/1.0 M HCl into toluene with a quaternary ammonium compound, Aliquat336. Anionic sulfate complexes of Mo and W with charge − 2 were extracted with Aliquat336 from H2SO4 solutions with concentrations of [H2SO4] > 2 M. In HF/1.0 M HCl, oxyfluoro complexes of Mo and W with charge − 1 were interpreted to be formed and extracted with Aliquat336. From these results, favorable conditions for the extraction of Sg are discussed. [ABSTRACT FROM AUTHOR]

Innenrücktitelbild: Chemical Characterization of a Volatile Dubnium Compound, DbOCl3 (Angew. Keywords: dubnium; gas chromatography; Group 5 elements; thermochemistry; transactinides EN dubnium gas chromatography Group 5 elements thermochemistry transactinides 18495 18495 1 08/05/21 20210809 NES 210809 B Die Gasphasenchemie b des exotischen Transactinoids Dubnium und seiner leichteren Homologen Tantal und Niob wird in der Zuschrift auf S. 18015 von Nadine M. Chiera, Tetsuya K. Sato und Mitarbeitern beschrieben. Dubnium, gas chromatography, Group 5 elements, thermochemistry, transactinides. [Extracted from the article]

Dubnium, gas chromatography, Group 5 elements, thermochemistry, transactinides Keywords: dubnium; gas chromatography; Group 5 elements; thermochemistry; transactinides EN dubnium gas chromatography Group 5 elements thermochemistry transactinides 18347 18347 1 08/05/21 20210809 NES 210809 B Extreme gas-phase chemistry b with the exotic transactinide dubnium and its lighter homologues tantalum and niobium is described by Nadine M. Chiera, Tetsuya K. Sato, and co-workers in their Communication on page 17871. Inside Back Cover: Chemical Characterization of a Volatile Dubnium Compound, DbOCl3 (Angew. [Extracted from the article]

The chemical characterization of the heaviest elements at the farthest reach of the periodic table (PT) and the classification of these elements in the PT are undoubtedly crucial and challenging subjects in chemical and physical sciences. The elucidation of the influence of relativistic effects on their outermost electronic configuration is also a critical and fascinating aspect. However, the heaviest elements with atomic numbers Z ≳ 100 must be produced at accelerators using nuclear reactions of heavy ions and target materials. Therefore, production rates for these elements are low, and their half-lives are as short as a few seconds to a few minutes; they are usually available in a quantity of only a few atoms at a time. Here, we review some highlighted studies on heavy actinide and light transactinide chemical characterization performed at the Japan Atomic Energy Agency tandem accelerator facility. We discuss briefly the prospects for future studies of the heaviest elements.

The sensitive analysis of 90 Sr with accelerator mass spectrometry (AMS) was developed to advance environmental radiology. One advantage of AMS is the ability to analyze environmental samples with 90 Sr/ 88 Sr atomic ratios of 10 -14 in following a simple chemical separation. Three different IAEA samples with known 90 Sr concentrations (moss-soil, animal bone, Syrian soil: 1 g each) were analyzed to assess the validity of the chemical separation and the AMS measurement. The 90 Sr measurements were conducted on the AMS system VERA combined with the Ion Laser InterAction Mass Spectrometry (ILIAMS) setup at the University of Vienna, which has excellent isobaric separation performance. The isobaric interference of 90 Zr in the 90 Sr AMS was first largely removed by chemical separation. The separation factor of Zr in two-step column chromatography with Sr resin and anion exchange resin was 10 6 . The 90 Zr remaining in the sample was effectively suppressed by ILIAMS. This procedure achieved a limit of detection <0.1 mBq in the 90 Sr AMS, which is lower than typical β-ray detection. The agreement between AMS measurements and nominal values for the 90 Sr concentrations of IAEA samples indicated that the new highly-sensitive 90 Sr analysis in the environmental samples with AMS is reliable.