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Journal Articles

Comparison of nuclear medicine therapeutics targeting PSMA among alpha-emitting nuclides

Kaneda, Kazuko*; Shirakami, Yoshifumi*; Kadonaga, Yuichiro*; Watabe, Tadashi*; Oe, Kazuhiro*; Yin, X.*; Haba, Hiromitsu*; Shirasaki, Kenji*; Kikunaga, Hidetoshi*; Tsukada, Kazuaki; et al.

International Journal of Molecular Sciences (Internet), 25(2), p.933_1 - 933_14, 2024/01

https://doi.org/10.3390/ijms25020933
 Times Cited Count：4 Percentile：89.63(Biochemistry & Molecular Biology)

Journal Articles

Optimized TES microcalorimeters with 14 eV energy resolution at 30 keV for $$gamma$$-ray measurements of the $$^{229}$$Th isomer

Muramatsu, Haruka*; Hayashi, Tasuku*; Yuasa, Naoki*; Konno, Ryohei*; Yamaguchi, Atsushi*; Mitsuda, Kazuhisa*; Yamasaki, Noriko*; Maehata, Keisuke*; Kikunaga, Hidetoshi*; Takimoto, Misaki; et al.

Journal of Low Temperature Physics, 200(5-6), p.452 - 460, 2020/09

https://doi.org/10.1007/s10909-020-02458-7
 Times Cited Count：2 Percentile：10.32(Physics, Applied)

Journal Articles

Production of $$^{266}$$Bh in the $$^{248}$$Cm($$^{23}$$Na,5$$n$$)$$^{266}$$Bh reaction and its decay properties

Haba, Hiromitsu*; Fan, F.*; Kaji, Daiya*; Kasamatsu, Yoshitaka*; Kikunaga, Hidetoshi*; Komori, Yukiko*; Kondo, Narumi*; Kudo, Hisaaki*; Morimoto, Koji*; Morita, Kosuke*; et al.

Physical Review C, 102(2), p.024625_1 - 024625_12, 2020/08

https://doi.org/10.1103/PhysRevC.102.024625
 Times Cited Count：6 Percentile：52.67(Physics, Nuclear)

Journal Articles

Energy of the $$^{229}$$Th nuclear clock isomer determined by absolute $$gamma$$-ray energy difference

Yamaguchi, Atsushi*; Muramatsu, Haruka*; Hayashi, Tasuku*; Yuasa, Naoki*; Nakamura, Keisuke; Takimoto, Misaki; Haba, Hiromitsu*; Konashi, Kenji*; Watanabe, Makoto*; Kikunaga, Hidetoshi*; et al.

Physical Review Letters, 123(22), p.222501_1 - 222501_6, 2019/11

https://doi.org/10.1103/PhysRevLett.123.222501
 Times Cited Count：44 Percentile：89.79(Physics, Multidisciplinary)

Journal Articles

Extraction behavior of rutherfordium as a cationic fluoride complex with a TTA chelate extractant from HF/HNO $$_{3}$$ acidic solutions

Yokoyama, Akihiko*; Kitayama, Yuta*; Fukuda, Yoshiki*; Kikunaga, Hidetoshi*; Murakami, Masashi*; Komori, Yukiko*; Yano, Shinya*; Haba, Hiromitsu*; Tsukada, Kazuaki; Toyoshima, Atsushi*

Radiochimica Acta, 107(1), p.27 - 32, 2019/01

https://doi.org/10.1515/ract-2018-2949
 Times Cited Count：1 Percentile：9.36(Chemistry, Inorganic & Nuclear)

Journal Articles

Performance of new gas-filled recoil ion separator GARIS-II for asymmetric fusion reaction

Kaji, Daiya*; Morimoto, Koji*; Wakabayashi, Yasuo*; Takeyama, Mirei*; Yamaki, Sayaka*; Tanaka, Kengo*; Haba, Hiromitsu*; Huang, M.*; Murakami, Masashi*; Kanaya, Jumpei*; et al.

JPS Conference Proceedings (Internet), 6, p.030107_1 - 030107_4, 2015/06

https://doi.org/10.7566/JPSCP.6.030107

Performance of the new gas-filled recoil ion separator GARIS-II was investigated using asymmetric $$^{22}$$Ne-induced fusion reactions. The use of He-H$$_{2}$$ mixture gas for the gas-filled magnet significantly reduced background scattered particles detected at the focal-plane Si detector, and increased a transmission of the asymmetric reaction products. A target-identification system was newly installed for efficient measurements of excitation functions without changing beam energy nor target.

Journal Articles

Production of $$^{88}$$Nb and $$^{170}$$Ta for chemical studies of element 105, Db, using the GARIS gas-jet system

Huang, M.*; Haba, Hiromitsu*; Murakami, Masashi*; Asai, Masato; Kaji, Daiya*; Kanaya, Jumpei*; Kasamatsu, Yoshitaka*; Kikunaga, Hidetoshi*; Kikutani, Yuki*; Komori, Yukiko*; et al.

Journal of Radioanalytical and Nuclear Chemistry, 304(2), p.845 - 849, 2015/05

https://doi.org/10.1007/s10967-014-3877-4
 Times Cited Count：3 Percentile：24.31(Chemistry, Analytical)

A technique to utilize radioisotopes of Nb and Ta was developed for chemical studies of element 105, Db, by coupling a gas-jet transport system to the RIKEN gas-filled recoil ion separator (GARIS). The short-lived $$^{88}$$Nb and $$^{170}$$Ta were produced with nuclear reactions using a $$^{19}$$F beam whose energy was the same as that to produce $$^{262}$$Db. Then, they were separated with GARIS and extracted to a chemistry laboratory with the gas-jet transport system. By changing only magnetic field of GARIS and inserting an energy degrader and a shutter for recoil ions, we could deliver the $$^{88}$$Nb and $$^{170}$$Ta to a chemistry device for $$^{262}$$Db without changing other experimental conditions.

Journal Articles

Production of $$^{256}$$Lr in the $$^{249,250,251}$$Cf + $$^{11}$$B, $$^{243}$$Am + $$^{18}$$O, and $$^{248}$$Cm + $$^{14}$$N reactions

Sato, Nozomi; Sato, Tetsuya; Asai, Masato; Toyoshima, Atsushi; Tsukada, Kazuaki; Li, Z.*; Nishio, Katsuhisa; Nagame, Yuichiro; Sch$"a$del, M.; Haba, Hiromitsu*; et al.

Radiochimica Acta, 102(3), p.211 - 219, 2014/03

https://doi.org/10.1515/ract-2014-2142
 Times Cited Count：10 Percentile：58.77(Chemistry, Inorganic & Nuclear)

Production cross-sections of the isotope $$^{256}$$Lr in the $$^{249,250,251}$$Cf + $$^{11}$$B, $$^{243}$$Am + $$^{18}$$O, and $$^{248}$$Cm + $$^{14}$$N reactions were measured using a He/KCl gas-jet transport system and a rotating wheel $$alpha$$-particle detection apparatus. The $$alpha$$-particle energy of $$^{256}$$Lr was distributed from 8.3 to 8.7 MeV and its half-life, $$T_{1/2}$$, was measured to be $$28 pm 1$$ s. The maximum cross sections in the $$^{249}$$Cf($$^{11}$$B, 4$$n$$)$$^{256}$$Lr and $$^{243}$$Am($$^{18}$$O, 5$$n$$)$$^{256}$$Lr reactions were determined to be $$122 pm 6$$ nb at the beam energy of 63 MeV and $$26 pm 3$$ nb at 96 MeV, respectively. In the $$^{248}$$Cm($$^{14}$$N, 6$$n$$)$$^{256}$$Lr reaction, the cross section was measured to be $$27 pm 1$$ nb at 91 MeV.

Journal Articles

Production of $$^{262}$$Db in the $$^{248}$$Cm($$^{19}$$F,5$$n$$)$$^{262}$$Db reaction and decay properties of $$^{262}$$Db and $$^{258}$$Lr

Haba, Hiromitsu*; Huang, M.*; Kaji, Daiya*; Kanaya, Jumpei*; Kudo, Yuki*; Morimoto, Koji*; Morita, Kosuke*; Murakami, Masashi*; Ozeki, Kazutaka*; Sakai, Ryutaro*; et al.

Physical Review C, 89(2), p.024618_1 - 024618_11, 2014/02

https://doi.org/10.1103/PhysRevC.89.024618
 Times Cited Count：26 Percentile：81.76(Physics, Nuclear)

Journal Articles

Excitation functions for production of Rf isotopes in the $$^{248}$$Cm + $$^{18}$$O reaction

Murakami, Masashi*; Goto, Shinichi*; Murayama, Hirofumi*; Kojima, Takayuki*; Kudo, Hisaaki*; Kaji, Daiya*; Morimoto, Koji*; Haba, Hiromitsu*; Kudo, Yuki*; Sumita, Takayuki*; et al.

Physical Review C, 88(2), p.024618_1 - 024618_8, 2013/08

https://doi.org/10.1103/PhysRevC.88.024618
 Times Cited Count：17 Percentile：70.48(Physics, Nuclear)

Production cross sections of Rf isotopes in the $$^{248}$$Cm + $$^{18}$$O reaction were measured at the beam energy range of 88.2 to 101.3 MeV by use of a gas-filled recoil ion separator. The excitation functions of $$^{260}$$Rf, $$^{261a}$$Rf, and $$^{262}$$Rf were obtained together with those of spontaneously fissioning nuclides which have few-second half-lives and have been assigned to $$^{261b}$$Rf and a longer-lived state of $$^{262}$$Rf. The excitation function of few-second spontaneously fissioning nuclide exhibited the maximum cross section at the $$^{18}$$O beam energy of 94.8 MeV. The shape of the excitation function was almost the same as that of $$^{261a}$$Rf, whereas it was quite different from those of $$^{260}$$Rf and $$^{262}$$Rf. A few-second spontaneously fissioning nuclide previously reported as $$^{261b}$$Rf and $$^{262}$$Rf observed in$$^{248}$$Cm + $$^{18}$$O reaction was identified as $$^{261b}$$Rf.

Journal Articles

Production of $$^{256}$$Lr in the $$^{248}$$Cm + $$^{14}$$N reaction

Sato, Nozomi; Sato, Tetsuya; Asai, Masato; Toyoshima, Atsushi; Tsukada, Kazuaki; Li, Z.*; Nishio, Katsuhisa; Nagame, Yuichiro; Sch$"a$del, M.; Haba, Hiromitsu*; et al.

RIKEN Accelerator Progress Report, Vol.46, P. 237, 2013/00

http://www.rarf.riken.jp/researcher/APR/Document/ProgressReport_vol_46.pdf

Due to the strong relativistic effects, the weakly-bound outermost electron results in a significantly low first ionization potential (IP) of Lr as compared with its neighboring heavy actinides. The isotope $$^{256}$$Lr, with a relatively long half-life of 27 s, is the suitable candidates for the IP measurement of Lr through the surface ionization method. In the present study, we measured the cross section of the $$^{248}$$Cm($$^{14}$$N, 6$$n$$)$$^{256}$$Lr reaction to evaluate the production rate of $$^{256}$$Lr. A $$^{248}$$Cm target with 960 $$pm$$ 60 $$mu$$g/cm$$^{2}$$ thickness was bombarded with a $$^{14}$$N$$^{5+}$$ beam from the RIKEN AVF Cyclotron. The beam energy was 91 MeV in the middle of the target. The average beam intensity was 1.2 particle-$$mu$$A. Reaction products were transported to the rotating wheel $$alpha$$-particle detection system with a He/KCl gas-jet system. The $$^{256}$$Lr cross section of 27$$pm$$1 nb was calculated based on the $$alpha$$-particle events between 8.3 and 8.7 MeV.

Journal Articles

New result in the production and decay of an isotope, $$^{278}$$113 of the 113th element

Morita, Kosuke*; Morimoto, Koji*; Kaji, Daiya*; Haba, Hiromitsu*; Ozeki, Kazutaka*; Kudo, Yuki*; Sumita, Takayuki*; Wakabayashi, Yasuo*; Yoneda, Akira*; Tanaka, Kengo*; et al.

Journal of the Physical Society of Japan, 81(10), p.103201_1 - 103201_4, 2012/10

https://doi.org/10.1143/JPSJ.81.103201
 Times Cited Count：175 Percentile：97.25(Physics, Multidisciplinary)

An isotope of the 113th element, $$^{278}$$113, was produced in a nuclear reaction with a $$^{70}$$Zn beam on a $$^{209}$$Bi target. We observed six consecutive $$alpha$$ decays following the implantation of a heavy particle in nearly the same position in the semiconductor detector, in extremely low background condition. The fifth and sixth decays are fully consistent with the sequential decays of $$^{262}$$Db and $$^{258}$$Lr both in decay energies and decay times. This indicates that the present decay chain consisted of $$^{278}$$113, $$^{274}$$Rg (Z = 111), $$^{270}$$Mt (Z = 109), $$^{266}$$Bh (Z = 107), $$^{262}$$Db (Z = 105), and $$^{258}$$Lr (Z = 103) with firm connections. This result, together with previously reported results from 2004 and 2007, conclusively leads the unambiguous production and identification of the isotope $$^{278}$$113, of the 113th element.

Journal Articles

Production of $$^{265}$$Sg in the $$^{248}$$Cm($$^{22}$$Ne,5$$n$$)$$^{265}$$Sg reaction and decay properties of two isomeric states in $$^{265}$$Sg

Haba, Hiromitsu*; Kaji, Daiya*; Kudo, Yuki*; Morimoto, Koji*; Morita, Kosuke*; Ozeki, Kazutaka*; Sakai, Ryutaro*; Sumita, Takayuki*; Yoneda, Akira*; Kasamatsu, Yoshitaka*; et al.

Physical Review C, 85(2), p.024611_1 - 024611_11, 2012/02

https://doi.org/10.1103/PhysRevC.85.024611
 Times Cited Count：55 Percentile：91.21(Physics, Nuclear)

Two isomeric states in $$^{265}$$Sg, i.e, $$^{265}$$Sg$$^{a}$$ and $$^{265}$$Sg$$^{b}$$ were produced in the $$^{248}$$Cm($$^{22}$$Ne,5$$n$$) reaction. Decay properties of $$^{265}$$Sg$$^{a,b}$$ were investigated with a rotating-wheel apparatus for $$alpha$$ and spontaneous fission (SF) spectrometry under low background condition attained by a gas-jet transport system coupled to the RIKEN gas-filled recoil ion separator. Based on genetically correlated $$alpha$$-$$alpha$$ (-$$alpha$$) and $$alpha$$-SF decay chains, 18 and 24 events were assigned to $$^{265}$$Sg$$^{a}$$ and $$^{265}$$Sg$$^{b}$$, respectively. The half-life and $$alpha$$-particle energy of $$^{265}$$Sg$$^{a}$$ were measured to be $$8.5^{+2.6}_{-1.6}$$ s and $$8.84 pm 0.05$$ MeV, respectively, and those of $$^{265}$$Sg$$^{b}$$ were $$14.4^{+3.7}_{-2.5}$$ s and $$8.69 pm 0.05$$ MeV.

Journal Articles

Anionic fluoro complex of element 105, Db

Kasamatsu, Yoshitaka*; Toyoshima, Atsushi; Asai, Masato; Tsukada, Kazuaki; Li, Z.; Ishii, Yasuo; Tome, Hayato*; Sato, Tetsuya; Kikuchi, Takahiro; Nishinaka, Ichiro; et al.

Chemistry Letters, 38(11), p.1084 - 1085, 2009/10

https://doi.org/10.1246/cl.2009.1084
 Times Cited Count：17 Percentile：51.09(Chemistry, Multidisciplinary)

We report on the characteristic anion-exchange behavior of the superheavy element dubnium (Db) with atomic number Z = 105 in HF/HNO$$_{3}$$ solution at the fluoride ion concentration [F$$^{-}$$] = 0.003 M. The result clearly demonstrates that the fluoro complex formation of Db is significantly different from that of the group-5 homologue Ta in the 6th period of the periodic table while the behavior of Db is similar to that of the lighter homologue Nb in the 5th period.

Journal Articles

Adsorption of Db and its homologues Nb and Ta, and the pseudo-homologue Pa on anion-exchange resin in HF solution

Tsukada, Kazuaki; Haba, Hiromitsu*; Asai, Masato; Toyoshima, Atsushi; Akiyama, Kazuhiko*; Kasamatsu, Yoshitaka; Nishinaka, Ichiro; Ichikawa, Shinichi; Yasuda, Kenichiro; Miyamoto, Yutaka; et al.

Radiochimica Acta, 97(2), p.83 - 89, 2009/02

https://doi.org/10.1524/ract.2009.1577
 Times Cited Count：22 Percentile：79.34(Chemistry, Inorganic & Nuclear)

Anion-exchange chromatography of element 105, dubnium (Db), produced in the $$^{248}$$Cm($$^{19}$$F, 5n)$$^{262}$$Db reaction is investigated together with the homologues Nb and Ta, and the pseudo-homologue Pa in 13.9 M hydrofluoric acid (HF) solution. The distribution coefficient (K$$_{d}$$) of Db on an anion-exchange resin is successfully determined by running cycles of the 1702 chromatographic column separations. The result clearly indicates that the adsorption of Db on the resin is significantly different from that of the homologues and that the adsorption of anionic fluoro complexes of these elements decreases in the sequence of Ta $$approx$$ Nb $$>$$ Db $$geq$$ Pa.

Journal Articles

Startup of superheavy element chemistry at RIKEN

Haba, Hiromitsu*; Akiyama, Takahiro*; Kaji, Daiya*; Kikunaga, Hidetoshi*; Kuribayashi, Takahiro*; Morimoto, Koji*; Morita, Kosuke*; Oe, Kazuhiro*; Sato, Nozomi*; Shinohara, Atsushi*; et al.

European Physical Journal D, 45(1), p.81 - 86, 2007/10

https://doi.org/10.1140/epjd/e2007-00135-4
 Times Cited Count：11 Percentile：48.98(Optics)

A review is given on the startup of the superheavy element (SHE) chemistry at RIKEN. A gas-jet transport system for the SHE chemistry has been coupled to the gas-filled recoil ion separator GARIS at the RIKEN Linear Accelerator. The performance of the system was appraised using $$^{206}$$Fr and $$^{245}$$Fm produced in the $$^{169}$$Tm($$^{40}$$Ar,3${it n}$)$$^{206}$$Fr and $$^{208}$$Pb($$^{40}$$Ar,3${it n}$)$$^{245}$$Fm reactions, respectively. The $$alpha$$ particles of $$^{206}$$Fr and $$^{245}$$Fm separated with GARIS and transported by the gas-jet were identified with a rotating wheel system for $$alpha$$ spectrometry under desired low background condition. The high gas-jet efficiencies over 80% were independent of the beam intensities up to 2 particle $$mu$$A. A gas-jet coupled target system for the production of SHEs was also installed on the beam line of the RIKEN K70 AVF cyclotron. The gas-jet transport of $$^{255}$$No and $$^{261}$$Rf produced in the $$^{238}$$U($$^{22}$$Ne,5${it n}$)$$^{255}$$No and $$^{248}$$Cm($$^{18}$$O,5${it n}$)$$^{261}$$Rf reactions, respectively, was conducted for the future chemical studies of $$^{265}$$Sg via the $$^{248}$$Cm($$^{22}$$Ne, 5${it n}$)$$^{265}$$Sg reaction.

Journal Articles

Observation of second decay chain from $$^{278}$$113

Morita, Kosuke*; Morimoto, Koji*; Kaji, Daiya*; Akiyama, Takahiro*; Goto, Shinichi*; Haba, Hiromitsu*; Ideguchi, Eiji*; Katori, Kenji*; Koura, Hiroyuki; Kikunaga, Hidetoshi*; et al.

Journal of the Physical Society of Japan, 76(4), p.045001_1 - 045001_2, 2007/04

https://doi.org/10.1143/JPSJ.76.045001
 Times Cited Count：203 Percentile：97.35(Physics, Multidisciplinary)

The production and decay of $$^{278}$$113 has been investigated using a gas-filled recoil ion separator in irradiations of $$^{209}$$Bi targets with $$^{70}$$Zn beam at 353 MeV. We have observed one $$alpha$$-decay chain that can be assigned to subsequent decays from $$^{278}$$113 produced in the $$^{209}$$Bi($$^{70}$$Zn,n) reaction. After emitting four consecutive $$alpha$$-particles, the both chains ended by spontaneous fission decays of $$^{262}$$Db and decay energies and decay times of the both chains obtained in the present work agree well with those reported by our group in 2004. The present result gives the first clear confirmation of the discovery of $$^{278}$$113 and its $$alpha$$-decay products $$^{274}$$Rg reported previously.

Journal Articles

Experiments on synthesis of the heaviest element at RIKEN

Morita, Kosuke*; Morimoto, Koji*; Kaji, Daiya*; Akiyama, Takahiro*; Goto, Shinichi*; Haba, Hiromitsu*; Ideguchi, Eiji*; Kanungo, R.*; Katori, Kenji*; Kikunaga, Hidetoshi*; et al.

AIP Conference Proceedings 891, p.3 - 9, 2007/03

https://doi.org/10.1063/1.2713494

A series of experiments studying the productions and their decays of the heaviest elements have been performed by using a gas-filled recoil separator GARIS at RIKEN. Results on the isotope of the 112th element, $$^{277}$$112, and on that of the 113th element, $$^{278}$$113, are reviewed. Two decay chains which are assigned to be ones originating from the isotope $$^{277}$$112 were observed in the $$^{208}$$Pb($$^{70}$$Zn, n) reaction. The results provide a confirmation of the production and decay of the isotope $$^{277}$$112 reported by a research group at GSI, Germany, produced via the same reaction by using a velocity filter. Two decay chains, both consisted of four consecutive alpha decays followed by a spontaneous fission, were observed also in the reaction $$^{209}$$Bi($$^{70}$$Zn, n). Those are assigned to be the convincing candidate events of the isotope of the 113th element, $$^{278}$$113, and its daughter nuclei. $$^{274}$$Rg, $$^{270}$$Mt, $$^{266}$$Bh, and $$^{262}$$Db.

Journal Articles

Extraction behavior of rutherfordium into tributylphosphate from hydrochloric acid

Haba, Hiromitsu*; Tsukada, Kazuaki; Asai, Masato; Toyoshima, Atsushi; Ishii, Yasuo; Tome, Hayato; Sato, Tetsuya; Nishinaka, Ichiro; Ichikawa, Takatoshi; Ichikawa, Shinichi; et al.

Radiochimica Acta, 95(1), p.1 - 6, 2007/01

https://doi.org/10.1524/ract.2007.95.1.1
 Times Cited Count：16 Percentile：71.20(Chemistry, Inorganic & Nuclear)

no abstracts in English

Journal Articles

Chemical studies on rutherfordium (Rf) at JAERI

Nagame, Yuichiro; Tsukada, Kazuaki; Asai, Masato; Toyoshima, Atsushi; Akiyama, Kazuhiko; Ishii, Yasuo; Sato, Tetsuya; Hirata, Masaru; Nishinaka, Ichiro; Ichikawa, Shinichi; et al.

Radiochimica Acta, 93(9-10), p.519 - 526, 2005/00

https://doi.org/10.1524/ract.2005.93.9-10.519
 Times Cited Count：31 Percentile：87.27(Chemistry, Inorganic & Nuclear)

no abstracts in English

40 (Records 1-20 displayed on this page)