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Sasaki, Yuji; Morita, Keisuke; Saeki, Morihisa*; Hisamatsu, Shugo*; Yoshizuka, Kazuharu*
Proceedings of 21st International Solvent Extraction Conference (ISEC 2017) (Internet), p.131 - 134, 2017/11
Three tridentate extractants including soft and hard donor has been developed and examined. The extractants are termed as 
-tetraoctyl-diglycolamide (TODGA), methylimino-
-dioctylacetamide (MIDOA) and -tetraoctyl-thiodiglycolamide (TDGA). The results of the present study show that TODGA can extract completely lanthanides and actinides, MIDOA can extract palladium, technetium, and rhenium, and TDGA can extract palladium, silver, and gold. We can compare the distribution ratios of these metals by TODGA, MIDOA, and TDGA. These results can be supported by some spectrometric studies, i.e., IR, NMR and UV, and calculations of metal complexes.
Hisamatsu, Shugo; Suzuki, Shinichi; Komoto, Shigeo*; Kishikawa, Keiki*; Yamamoto, Yusuke*; Motokawa, Ryuhei; Yaita, Tsuyoshi
Tetrahedron, 73(27-28), p.3993 - 3998, 2017/07
Times Cited Count：15 Percentile：57.79(Chemistry, Organic)Sasaki, Yuji; Morita, Keisuke; Saeki, Morihisa*; Hisamatsu, Shugo; Yoshizuka, Kazuharu*
Hydrometallurgy, 169, p.576 - 584, 2017/05
Times Cited Count：14 Percentile：56.4(Metallurgy & Metallurgical Engineering)The novel tridentate extractant including soft donor has developed and examined. The extractant, tetraoctyl-thiodiglycolamide (TDGA), is analogous structure to tetraoctyl-diglycolamide (TODGA) and methylimino-dioctylacetamide (MIDOA), but with sulfur donor instead of ether oxygen or nitrogen atoms of TODGA or MIDOA. From the present work, TDGA can extract silver, palladium, gold, and mercury from acidic solutions to n-dodecane. In addition to these results, the distribution ratios of hard and soft acid metals by using TDGA, TODGA, and MIDOA are compared, where the metal-complexations with each donor atom are investigated. 1H-NMR and IR studies for the metal-TDGA complexes indicate the role on donor atoms, S and N, of TDGA.
Komoto, Shigeo*; Chuko, Tomotaka*; Hisamatsu, Shugo; Okuda, Yasuhiro*; Masu, Hyuma*; Takahashi, Masahiro*; Kishikawa, Keiki*
Crystal Growth & Design, 15(6), p.2723 - 2731, 2015/05
Times Cited Count：16 Percentile：75.03(Chemistry, Multidisciplinary)Piezoluminescence and liquid crystallinity of anthracene-based bispyridinium salts were investigated in stimulus responsive luminescent organic crystals and luminescent ionic liquid crystals. The salts possess an anthracene moiety as a fluorophore in their center, and the pyridiniums attached to the anthracene moiety are substituted with trialkoxybenzyl groups. Single crystals of the salts bearing two trimethoxybenzyl groups were obtained as solvates. Ethyl acetate, acetone, and dioxane solvates of the chlorides have almost the same crystal structures with one-dimensional channels. Grinding of the solvated crystals caused the extrusion of the included solvent molecules, which resulted in the red shifts of their fluorescence in the solid state. Tris(octyloxy)benzyl and tris(dodecyloxy)benzyl derivatives exhibited rectangular columnar liquid crystals upon being heated for their bromide and tetrafluoroborate salts and upon being cooled for their hexafluorophosphate salts.
Hisamatsu, Shugo; Masu, Hyuma*; Takahashi, Masahiro*; Kishikawa, Keiki*; Komoto, Shigeo*
Crystal Growth & Design, 15(5), p.2291 - 2302, 2015/04
Times Cited Count：77 Percentile：98.08(Chemistry, Multidisciplinary)Anthracene derivatives possessing a carbamate group and an ester group at their 9- and 10-positions, respectively, were prepared to furnish pairwise packing of anthracene fluorophores in their crystal structures. They were nonluminescent in ethanol solution and showed AIE (aggregation-induced emission) in aqueous ethanol solution and in solid state. Crystal structure analysis of them showed that the H-bonding networks involved in their crystal structures could be classified into four patterns, H-bonding between the carbamate and the ester carbonyl (motifA), H-bonding between the carbamate and the ester oxygen atom (motif B), H-bonded cyclic dimer of carbamate moieties (motif C), and H-bonded chain among carbamate moieties (motif D). Compounds with pairwisely packed anthracene fluorophores showed dimer emission with the longer fluorescence wavelength than others without the pair formation.
Hisamatsu, Shugo; Suzuki, Shinichi; Yaita, Tsuyoshi
no journal, ,
A novel sensory system incorporated with an amplification function was devised for detection of trace-level substances. This sensory system comprises three steps, namely, recognition, amplification, and chemiluminescence. These steps were linked with chemical reactions and were induced continuously. The process from amplification to chemiluminescence was accomplished in the system using fluoride ions. The amplification was based on a self-immolative system, which permitted detection of the emission even at low concentration of fluoride ions for the system wherein chemiluminescence cannot be induced in the absence of fluoride ions. A suitable ratio of the chemiluminescent compound and the amplifier was optimized for efficient amplification.
