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Journal Articles

Effect of the headgroup structure on counterion binding in adsorbed surfactant films investigated by total reflection X-ray absorption fine structure spectroscopy

Imai, Yosuke*; Tokiwa, Yuhei*; Ueno, Shusaku*; Tanida, Hajime; Watanabe, Iwao*; Matsubara, Hiroki*; Takiue, Takanori*; Aratono, Makoto*

Bulletin of the Chemical Society of Japan, 91(10), p.1487 - 1494, 2018/10

https://doi.org/10.1246/bcsj.20180167

Times Cited Count：0 Percentile：100(Chemistry, Multidisciplinary)

Competitive binding of binary mixed counterions to the headgroups of adsorbed surfactant films has been investigated at solution surfaces by total reflection X-ray absorption fine structure (XAFS) spectroscopy. The obtained extended XAFS spectra for bromide counterions are linear combinations of the spectra of fully hydrated bromide ions (free Br) and partially dehydrated bromide ions bound to the headgroups of the surfactant ions (bound Br). From the fraction of bound Br in counterion mixed systems, two series of the relative strengths of counterion binding are proposed for the trimethylammonium (TA $^{+}$ ) and 3-methylimidazolium (MIM $^{+}$ ) headgroups: (a) TA-SO $_{4}$ TA-Cl TA-Br TA-BF $_{4}$ and (b) MIM-Br TA-Br TA-BF $_{4}$ MIM-BF $_{4}$ . For the TA headgroup, matching the hydration of the headgroups and counterions gives series (a) according to Collins' law, which states that the tendency of contact ion pair formation becomes larger when the absolute values of the hydration enthalpies of the ions match. For the MIM headgroup, the number of binding sites of hydrogen bonds between the MIM headgroup and counterion is essential, which leads to series (b) because of competition between the counterion and water for interaction with the MIM headgroup.

Journal Articles

Optical properties of trinuclear citrate complexes containing 4f and 5f block metals

Aoyagi, Noboru; Palladino, G.*; Nagasaki, Shinya*; Kimura, Takaumi

Bulletin of the Chemical Society of Japan, 91(6), p.882 - 890, 2018/06

https://doi.org/10.1246/bcsj.20170419

Times Cited Count：1 Percentile：89.35(Chemistry, Multidisciplinary)

The speciation and coordination geometries of M(III)-citrate complexes in aqueous solutions, where M denotes Eu, Tb, Lu, or Cm, are studied using potentiometric titration, nuclear magnetic resonance spectroscopies. Their photophysical properties are also characterized by time-resolved fluorescence spectra. The formation constants of mononuclear, dinuclear, and trinuclear Lu-citrate species were determined by potentiometric titration in 3.00 M NaClO $_{4}$ aqueous media. Terminal carboxylic conformation in trinuclear complexes comprised both the five- and six-membered rings at different exchanging rates. Hydration states evaluated for Eu $^{3+}$ ions are the chemical formula of [Eu(Cit) $_{2}$ (H $_{2}$ O) $_{2.5}$ ] $^{3-}$ and [Eu $_{3}$ (OH) $_{4}$ (Cit) $_{4}$ (H $_{2}$ O) $_{3.4}$ ] $^{7-}$ . These complexes in aqueous solution have geometrical similarity to the crystal structures in the literature. Furthermore, the entity of the hetero-trinuclear complex induces the intramolecular energy transfer from Tb $^{3+}$ to Eu $^{3+}$ . The incorporation of Cm $^{3+}$ into these homo/hetero-trinuclear citrate complexes proved to be a successful trial to probe the formation of actinide polymer at a trace level.

Journal Articles

Molybdenum adsorption properties of alumina-embedded mesoporous silica for medical radioisotope production

Saptiama, I.*; Kaneti, Y. V.*; Oveisi, H.*; Suzuki, Yoshitaka; Tsuchiya, Kunihiko; Takai, Kimiko*; Sakae, Takeji*; Pradhan, S.*; Hossain, M. S. A.*; Fukumitsu, Nobuyoshi*; et al.

Bulletin of the Chemical Society of Japan, 91(2), p.195 - 200, 2018/02

https://doi.org/10.1246/bcsj.20170295

Times Cited Count：31 Percentile：7.8(Chemistry, Multidisciplinary)

no abstracts in English

Journal Articles

Mesoporous alumina as an effective adsorbent for molybdenum (Mo) toward Instant production of radioisotope for medical use

Saptiama, I.*; Kaneti, Y. V.*; Suzuki, Yumi*; Suzuki, Yoshitaka; Tsuchiya, Kunihiko; Sakae, Takeji*; Takai, Kimiko*; Fukumitsu, Nobuyoshi*; Alothman, Z. A.*; Hossain, M. S. A.*; et al.

Bulletin of the Chemical Society of Japan, 90(10), p.1174 - 1179, 2017/10

https://doi.org/10.1246/bcsj.20170184

Times Cited Count：34 Percentile：11.47(Chemistry, Multidisciplinary)

no abstracts in English

Journal Articles

Bithiophene with winding vine-shaped molecular asymmetry; Preparation, structural characterization, and enantioselective synthesis

Toyomori, Yuka*; Tsuji, Satoru*; Mitsuda, Shinobu*; Okayama, Yoichi*; Ashida, Shiomi*; Mori, Atsunori*; Kobayashi, Toru; Miyazaki, Yuji; Yaita, Tsuyoshi; Arae, Sachie*; et al.

Bulletin of the Chemical Society of Japan, 89(12), p.1480 - 1486, 2016/09

https://doi.org/10.1246/bcsj.20160265

Times Cited Count：5 Percentile：69.82(Chemistry, Multidisciplinary)

Journal Articles

Recovery of Rhodium(III) from nitric acid solutions using adsorbent functionalized with -trimethylglycine

Suzuki, Tomoya; Morita, Keisuke; Sasaki, Yuji; Matsumura, Tatsuro

Bulletin of the Chemical Society of Japan, 89(5), p.608 - 616, 2016/05

https://doi.org/10.1246/bcsj.20160007

Times Cited Count：3 Percentile：80.64(Chemistry, Multidisciplinary)

In a previous study, we found that AMP03 adsorbs Rh(III) from the HNO $_{3}$ solution with pH = 1.7 - 2.2. In this study, to understand the Rh(III) adsorption properties of AMP03 and clarify conditions for efficient recovery, we investigated the adsorption behaviors of Rh(III) from the HNO $_{3}$ solution. As a result, it was found that Rh(III) is effectively adsorbed from aqueous solution containing low H $^{+}$ and high NO $_{3}$ $^{-}$ concentration. Considering the adsorption mechanism of Rh(III), we found that Rh $^{3+}$ in aqueous solution is adsorbed with two betaine groups in AMP03 and three NO $_{3}$ $^{-}$ .

Journal Articles

Development of nondestructive and quantitative elemental analysis method using calibration curve between muonic X-ray intensity and elemental composition in bronze

Ninomiya, Kazuhiko; Nagatomo, Takashi*; Kubo, Kenya*; Ito, Takashi; Higemoto, Wataru; Kita, Makoto*; Shinohara, Atsushi*; Strasser, P.*; Kawamura, Naritoshi*; Shimomura, Koichiro*; et al.

Bulletin of the Chemical Society of Japan, 85(2), p.228 - 230, 2012/02

https://doi.org/10.1246/bcsj.20110151

Times Cited Count：13 Percentile：52.4(Chemistry, Multidisciplinary)

Elemental analysis of bulk materials can be performed by detecting the high-energy X-rays emitted from muonic atoms. Muon irradiation of standard bronze samples was performed to determine the muon capture probabilities for the elemental components from muonic X-ray spectra. Nondestructive elemental analysis of an ancient Chinese coin was also performed.

Journal Articles

Fluorido complex formation of element 104, rutherfordium (Rf)

Ishii, Yasuo; Toyoshima, Atsushi; Tsukada, Kazuaki; Asai, Masato; Li, Z.*; Nagame, Yuichiro; Miyashita, Sunao*; Mori, Tomotaka*; Suganuma, Hideo*; Haba, Hiromitsu*; et al.

Bulletin of the Chemical Society of Japan, 84(9), p.903 - 911, 2011/09

https://doi.org/10.1246/bcsj.20110126

Times Cited Count：14 Percentile：50.57(Chemistry, Multidisciplinary)

The cation-exchange behavior of element 104, rutherfordium (Rf), was investigated together with its lighter group-4 homologues Zr and Hf, and the tetravalent pseudo-homologue Th in HF/HNO $_{3}$ mixed solution. The results demonstrate that distribution coefficients ( $K_{d}$ ) of Rf in HF/0.10 M HNO $_{3}$ decrease with increasing concentration of the fluoride ion [F $^{-}$ ], indicating the consecutive formation of fluorido complexes of Rf. We also measured the $K_{d}$ values of Rf and the homologues as a function of the hydrogen ion concentration [H $^{+}$ ]. The log $K_{d}$ values decrease linearly with an increase of log [H $^{+}$ ] with slopes between -2.1 and -2.5. This indicates that these elements are likely to form the same chemical compounds: mixture of [MF] $^{3+}$ and [MF $_{2}$ ] $^{2+}$ (M = Rf, Zr, Hf and Th) in the studied solution. It is also ascertained that sequence in the fluoride complex formation is Zr Hf Rf Th.

Journal Articles

Chloride complexation of Zr and Hf in HCl investigated by extended X-ray absorption fine structure spectroscopy; Toward characterization of chloride complexation of element 104, rutherfordium (Rf)

Haba, Hiromitsu*; Akiyama, Kazuhiko*; Tsukada, Kazuaki; Asai, Masato; Toyoshima, Atsushi; Yaita, Tsuyoshi; Hirata, Masaru; Sueki, Keisuke*; Nagame, Yuichiro

Bulletin of the Chemical Society of Japan, 82(6), p.698 - 703, 2009/06

https://doi.org/10.1246/bcsj.82.698

Times Cited Count：10 Percentile：57.16(Chemistry, Multidisciplinary)

Chloride complexation of the group-4 elements Zr and Hf in 8.0-11.9 M HCl is investigated by Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy to characterize chloro complexes of the transactinide element, rutherfordium (Rf). The complexes of Zr and Hf successively vary with the concentration of HCl from a hydrated complex [M(H $_{2}$ O) $_{8}$ ] $^{4+}$ at 8.0 M to a hexachloro complex [MCl $_{6}$ ] $^{2-}$ at 11.9 M (M = Zr and Hf). The present structural changes of the Zr and Hf complexes well reflect the previously studied anion-exchange behavior of Zr and Hf in HCl. From both the EXAFS and anion-exchange results, we suggest that Rf forms the same complexes as those of Zr and Hf in HCl, and that the complexation strength of the hexachloro complexes of the group-4 elements, [MCl $_{6}$ ] $^{2-}$ (M = Zr, Hf, and Rf), is in the sequence of Rf Zr Hf.

Journal Articles

Control of coordination and luminescence properties of lanthanide complexes using octadentate oligopyridine-amine ligands

Wada, Atsushi*; Watanabe, Masayuki; Yamanoi, Yoshinori*; Nankawa, Takuya; Namiki, Kosuke*; Yamasaki, Mikio*; Murata, Masaki*; Nishihara, Hiroshi*

Bulletin of the Chemical Society of Japan, 80(2), p.335 - 345, 2007/02

https://doi.org/10.1246/bcsj.80.335

Times Cited Count：18 Percentile：44.39(Chemistry, Multidisciplinary)

Lanthanide complexes with linear and cyclic octadentate oligopyridine-amine ligands were synthesized, and their molecular structures were determined by single-crystal X-ray crystallography. All of the complexes had a distorted capped square antiprism (CSAP) geometry, and the coordination environments of lanthanide complexes were more distortedfor the complexes with the linear ligand than those with the cyclic ligand. The Eu $^{3+}$ complexes with the linear ligand showed more intense emissions, which were attributed to the $^{5}$ D $_{0}$ $^{7}$ F $_{2}$ transition, than the complex withthe cyclic ligand in acetonitrile, which can be attributed to the distortion in the coordination environments. These results indicate that the coordination environments of lanthanide complexes, and thus the luminescence properties, can be controlled by tuning the geometrical structures of polydentate ligands.

Journal Articles

Component analysis of particulate products in electron beam-irradiated Xylene/air mixtures using an atmospheric pressure ionizing mass spectrometer

Hakoda, Teruyuki; Sako, Toshihiro*; Shimada, Akihiko; Ishida, Tsuneo*; Kojima, Takuji

Bulletin of the Chemical Society of Japan, 79(5), p.731 - 737, 2006/05

https://doi.org/10.1246/bcsj.79.731

Times Cited Count：5 Percentile：71.71(Chemistry, Multidisciplinary)

no abstracts in English

Journal Articles

Decomposition behavior of PCDD/F isomers in incinerator gases under electron-beam irradiation

Hirota, Koichi; Kojima, Takuji

Bulletin of the Chemical Society of Japan, 78(9), p.1685 - 1690, 2005/09

https://doi.org/10.1246/bcsj.78.1685

Times Cited Count：7 Percentile：66.38(Chemistry, Multidisciplinary)

Decomposition behavior under electron-beam irradiation was examined for polychlorinated dibenzo-p-dioxin (PCDD) and polychlorinated dibenzofuran (PCDF) isomers in incinerator gases. Significant decomposition was obtained for all PCDD isomers over the investigated absorbed doses, which was resulted from oxidation reactions with OH radicals yielded by electron-beam irradiation. In the case of PCDFs, specific isomers having symmetrical structures such as 1, 2, 8, 9-, 2, 3, 7, 8-, and 3, 4, 6, 7-TeCDFs were yielded through the dechlorination of PeCDF isomers. Thermal electrons probably played a role in the dechlorination of PeCDF isomers.

Journal Articles

Decomposition of phenolic endocrine disrupting chemicals by potassium permanganate and -ray irradiation

Abe, Yasuhiro*; Takigami, Machiko; Sugino, Koji*; Taguchi, Mitsumasa; Kojima, Takuji; Umemura, Tomonari*; Tsunoda, Kinichi*

Bulletin of the Chemical Society of Japan, 76(8), p.1681 - 1685, 2003/08

https://doi.org/10.1246/bcsj.76.1681

Times Cited Count：5 Percentile：72.28(Chemistry, Multidisciplinary)

The decomposition of phenolic endocrine disrupting chemicals (P-EDCs), such as phenol, 4-butylphenol (BuP), and bisphenol A (BPA), in aqueous solutions by potassium permanganate (KMnO $_{4}$ ) was studied and its efficiency was compared with that of hydroxyl radicals (OH $^{.}$ ) generated by $^{60}$ Co -ray irradiation. Various organic acids and inorganic carbon were formed in the decomposition of P-EDCs due to either KMnO $_{4}$ or OH $^{.}$ . They were formed via direct aromatic ring cleavage in the case of KMnO $_{4}$ and OH $^{.}$ addition-substitution reactions followed by aromatic ring cleavage in the case of OH $^{.}$ . Comparing the decrease in the P-EDCs based on the number of electrons, the amount of KMnO $_{4}$ spent to completely eliminate BuP and BPA was comparable to the amount of OH $^{.}$ . Although three times more KMnO $_{4}$ was needed for phenol than OH $^{.}$ , the complete conversion of phenol into organic acids and inorganic carbon was achieved with 720M of electrons in both cases.