Chemical Society of Japan

J. Jaques, A. CoUet, and S. WiUen, Enantiomers, Racemate, and Resolutions,]o m Wiley Sons, Inc., New York, 1981 The Chemical Society of Japan, eds., Kikan Kagaku Sosetsu (No. 6, Resolution of Optical Isomers), Gakkai Shuppan Senta, Tokyo, Japan, 1989 G. C. Barrett ia Ref. 1, Chapt. 10, pp. 338—353 S. Otsuka and T. Mukaiyama, Progress of ylsymmetric Synthesis and Optical Resolution (ia Japanese), Kagaku Dojia, Kyoto, Japan, 1982. 

N. Oi ia Chemical Society of Japan, eds., Kagaku Sosetsu (No. 6, Resolution of Optical Isomers), Gakkai Shuppan Senta, Tokyo, Japan, 1989,... 

S. B 2ick cn2cn, Mmino Mcid Determination Methods and Techniques, Marcel Dekker, New York, 1968 A. Niederweiser and G. Pataki, eds., Neiv Techniques in Mmino Mcids, Peptide and Protein Mnalysis, Ann Arbor Science Pubhshers, Ann Arbor, Mich., 1971 The Chemical Society of Japan, eds., Neiv Experimental Chemistry Series, Vol. 1 (Biochemistry 1) (in Japanese), Mamzen, Tokyo, Japan, 1978, pp. 141—160. 

Federation of Asian Chemical Societies (FACS) / The Chemical Society of Japan... 

Chemical Manufacturers Association (CMA), See American Chemistry Council (ACC), 270 Chemical Products Corporation, 223 Chemical Services Ltd., 198-199 Chemical Society of Japan, 261 Chemical Society of Peni (SQP), 263... 

FaBeChim - VeBeVeChem, 257 Fad Europe S.p.A., 179 Faimiount Chemical Company, 228 Far Research Inc., 228 Farmland Industries, 228 Federal Department for the Envhonment, 281 Federal Environment Agency Ltd. - Austria, 281 Federal Environmental Agency (UBA), 282 Federation of Asian Chemical Societies (FACS) / The Chemical Society of Japan, 261... 

Taguchi, H., Matsuzawa, M., and Ohta, T. (1980). Data presented at the annual meeting of the Agricultural Chemical Society of Japan, (April 1980). 

H. Murakami, Y. Kobayashi, T. Shimizu, and N. Kamigata, 73rd Annual Meeting of the Chemical Society of Japan, September 1997, Morioka, Abstract Book, p. 316. 

S. Tozume, T. Yagihara, S. Ando, and T, Migita, 21st Annual Meeting of the Chemical Society of Japan, p. 1791 (1969). 

Fig. 2. Geometries calculated (solid lines) and observed (bold dashed lines) for 1-propanol in its a-cyclodextrin adduct. G3 and G6 denote the numbers of glucopyranose units of a-cyclodextrin. H3 and H5 refer to the hydrogen atoms located inside of the cyclodextrin cavity. The hydrogen atoms for the observed geometry of 1-propanol are not shown, since their atomic coordinates have not been determined. The observed 1-propanol is twofold disordered, with site a occupied 80%, site b 20%. Interatomic distances are shown in bold italics on fine dashed lines (nm). Reproduced with permission from the Chemical Society of Japan...

Fig. 4. Plots of log 1 /Kd vs. log Pe for complexes of a-cyclodextrin with branched alkanols (O) and cycloalkanols ( ). The solid line was given by the plots for an a-cyclodextrin-1-alkanol system. Numbers shown refer to the numbers in the first column of Table 2. Reproduced with permission from the Chemical Society of Japan...

The Chemical Society of Japan, Kai ku-Binnninn Kisohenn Kaitei 5 Harm (Chemical Handbook,... 

The Chemical Society of Japan edited by Y. Iwasam, N.Oyama and H.Kunieda... 

Makide Y, Tominaga T, Rowland FS. 1979. [Gas chromatographic analysis of halogenated hydrocarbons in air over Japan.] Chemistry Lett (Chemical Society of Japan) 4 355-358. (Japanese)... 

Muto, N., Komatsu, T. Nakagawa, T. (1973). Counterion effect on the titration behaviour of poly(maleic acid). Bulletin of the Chemical Society of Japan, 46, 2711-15. 

Diastereoselective allylation of aromatic aldehyde. Bulletin of the Chemical Society of Japan, 68, 1523. 

FigureS.7 Near-field two-photon excitation images of single gold nanorods detected by two-photon induced photoluminescence. Nanorod dimensions (length, diameter) are 540 nm, 20 nm for (a) and 565 nm, 21 nm in (b). Scale bars lOOnm. (Reproduced with permission from The Chemical Society of Japan [11]).

Figure 11. X-ray diffraction patterns of PVP-protected metal nanoparticles (a) PVP-protected CuPd (Cu Pd = 2 1) bimetallic nanoparticles (b) PVP-protected Pd nanoparticles (c) PVP-protected Cu dispersion (d) physical mixture of (b) and (c) (Cu Pd = 2 1). (Reprinted from Ref [71], 1993, with permission from The Chemical Society of Japan.)...

Figure 6. Influence of the molar ratio of precursors on the Fe content of FePt nanoparticles. The dashed line indicates the Fe content in feeing precursors. (Reprinted from Ref. [19], 2004, The Chemical Society of Japan.)...

Source Reprinted from Ref [19], 2004, with permission from The Chemical Society of Japan. Mole ratio of precursors. 

Amsterdam, 2001, 323 (b) T. Sugimoto, Y. Shintoku, A. Muramatsu, Proceedings of 72nd Annual Meeting, Chemical Society of Japan 1 (1997) 90. 

FIG. 8 Dependence of the adsorbed amount of C12E4 on the applied potential. Concentration of C12E4 in nitrobenzene is 50 (curve 1), 20 (curve 2), 10 (curve 3), and 5 (curve 4)mmoldm (From Ref. 47, reproduced by permission. The Chemical Society of Japan.)... 

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