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| 1.
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論文
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Ihara, Yoshinori ; Tsuchiya, Ryokichi
概要:
The following ten nickel(II) complexes with meso- or dl-1,2-diphenyl-1,2-ethanediamine (abbreviated as meso-stien and dl-stien, respectively) were prepared, and their thermal behavior was investigated in the
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solid phase: [Ni(meso-stien)2]X2 (X=Cl, Br, I, NO3, or ClO4), [Ni(dl-stien)2]X2 (X=I or ClO4), and [Ni(H2O)2(dl-stien)2]X2 (X=Cl, Br, or NO3). The square planar bis(dl-stien) complex chloride, bromide, and nitrate obtained by thermal dehydration of their respective octahedral diaqua complexes were found by various techniques to be transformed, upon further heating, to the octahedral diacido bis(dl-stien) complexes. The complexes containing dl-stien have a stronger tendency to show such structural transformations than those containing meso-stien. The reason for this difference is discussed.
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| 2.
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translated from the original Sanskrit with introduction and notes by Kamaleswar Bhattacharya ; text critically edited by E.H. Johnston and Arnold Kunst
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| 3.
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translations and studies by Chr. Lindtner
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| 4.
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Nāgārjuna ; introduction, Sanskrit text, English translation, and annotation, David J. Kalupahana
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edited by C. Robert Helms and Bruce E. Deal
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| 6.
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Yoshimura, Osamu ; Ueda, Kazumasa ; Yamamoto, Yoshikazu
概要:
2-(2-Thiazolylazo)-4-methoxyphenol (TAMP) forms a brownish 2:1 complex with iron(ll) in the presence of ascorbic acid; t
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he complex has a characteristic absorption at 784 nm in chloroform. By utilizing this peculiar absorption, selective spectrophotometry determination of iron has been developed. The optimum pH for iron extraction lies between 5.0-9.3 and Beer's law holds up to 5.0 ng/ml of iron. Many type of ions are tolerable. The method was successfully applied to the determination of iron in river waters. The extraction constant of iron(ll) complex was log Kex=-2.50±0.12 and the extraction mechanism was kinetically investigated. The complexation rate was first-order with respect to iron(ll) and TAMP concentrations and independent of ascorbic acid concentration. From these results, the major extraction rate-determining step was concluded to be a 1:1 complexation reaction between iron(ll) and dissociated TAMP. Kinetic data and activation parameters for the first-order reaction were determined and discussed. © 1988, The Japan Society for Analytical Chemistry. All rights reserved.
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| 7.
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Sakurai, Ikuo ; Suzuki, Harumi ; Shimizu, Sakae ; Yamamoto, Yuzuru
概要:
It was found that Macrophoma commelinae (IFO 9570) had an ability to transform 5-acetyl-4-methoxy-6-methyl-2-pyrone (1) to 4-acetyl-3-methoxy-5-methylbenzoic acid (2). This biotransformation was investigated using 13C- and 14C-labeled
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compounds. It is likely that 2 is formed by condensation of the added 2-pyrone and a catabolic pyruvate.
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| 8.
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Kodama, Akio
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| 9.
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Suzuki, Masatatsu ; Uehara, Akira
概要:
Reaction of copper(II) ion with hexacyanoferrate(II) ion, [Fe(CN)6]4−, in an aqueous solution containing such an amine a
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s en (1,2-ethanediamine), tn (1,3-propanediamine), dien (bis(2-aminoethyl)amine), or dpt (bis(3-aminopropyl)amine), gave two types of complexes: Double complex salts, [Cu(en or tn)2]2[Fe(CN)6]·nH2O(n=5–8), and cyanide-bridged complexes, [(Cu(dien or dpt))2(NC)2Fe(CN)4]·4H2O. The infrared spectra of the complexes in the νCN region revealed that the complexes, [(Cu(dien or dpt))2(NC)2Fe(CN)4]·4H2O, contain cyanide bridges, while in [Cu(en or tn)2]2[Fe(CN)6]·nH2O, no cyanide bridge is present. The thermal reactions of the complexes in the solid state were investigated by means of derivatography under dynamic conditions (D conditions). It was found that dehydration from [Cu(en)2Fe(CN)6]·nH2O resulted in formation of cyanide bridge in the apical position of square planer [Cu(en)2]2+. For [(Cu(dien or dpt))2(NC)2Fe(CN)4]·4H2O, dehydration resulted in the formation of additional cyanide bridges. All the complexes showed metal to metal (iron(II) to copper(II)) charge-transfer transitions (MMCT) in the near ultraviolet or visible region. The complexes, [Cu(en or tn)2]2[Fe(CN)6]·nH2O, exhibited the outer sphere iron(II) to copper(II) charge-transfer bands (OSMMCT) in the near ultra-violet region. [(Cu(dien or dpt))2(NC)2Fe(CN)4]·4H2O and the dehydrated complexes prepared by thermal reaction showed the inner-sphere iron(II) to copper(II) charge transfer bands (ISMMCT) in the visible region. A good correlation was observed between the energies of the MMCT and the d-d band maxima of copper(II) ions.
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| 10.
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