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  • 1
    Publication Date: 2014-08-30
    Description: Author(s): K. Kimura, S. Nakatsuji, and T. Kimura Several pyrochlore antiferromagnets are being considered as candidate materials where geometrical frustration may lead to quantum spin-liquid states. In a “breathing” pyrochlore lattice systems (see PRL 110, 097203 (2013)) the spins occupy the vertices of alternating tetrahedra of different size that are characterized by different exchange parameters J and J ′ . [Phys. Rev. B 90, 060414] Published Fri Aug 29, 2014
    Keywords: Magnetism
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
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  • 2
    Publication Date: 2018-04-19
    Description: Author(s): K. Kimura, M. Toyoda, P. Babkevich, K. Yamauchi, M. Sera, V. Nassif, H. M. Rønnow, and T. Kimura A material with broken space-inversion and time-reversal symmetries can exhibit symmetry-dependent unique phenomena such as the magnetoelectric effect. Ferroic order of magnetic quadrupoles fulfills this symmetry condition. The authors report here the discovery of ferroic magnetic quadrupole order and its magnetoelectric activity in the novel compound Pb(TiO)Cu 4 (PO 4 ) 4 , which is in contrast with isostructural Ba(TiO)Cu 4 (PO 4 ) 4 and Sr(TiO)Cu 4 (PO 4 ) 4 in exhibiting antiferroic quadrupole order. Their first-principles calculations reveal that s 2 electrons in Pb 2 + ions alter specific magnetic interactions and consequently switch the quadrupole order from antiferroic to ferroic. This result provides not only an opportunity to explore magnetoelectric phenomena arising from magnetic quadrupoles, but also a useful way of fine-tuning magnetic interactions with s 2 electrons. [Phys. Rev. B 97, 134418] Published Wed Apr 18, 2018
    Keywords: Magnetism
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
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  • 3
    Publication Date: 2017-12-27
    Description: Author(s): P. Babkevich, L. Testa, K. Kimura, T. Kimura, G. S. Tucker, B. Roessli, and H. M. Rønnow The antiferromagnetic compound Ba ( TiO ) Cu 4 ( PO 4 ) 4 contains square cupola of corner-sharing CuO 4 plaquettes, which were proposed to form effective quadrupolar order. To identify the magnetic structure, we have performed spherical neutron polarimetry measurements. Based on symmetry analysis and careful ... [Phys. Rev. B 96, 214436] Published Tue Dec 26, 2017
    Keywords: Magnetism
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 9 (1977), S. 116-117 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic solvent-induced shifts (ASIS) in 19F n.m.r. spectra of several organic fluoro compounds have been determined in several solvents. 19F n.m.r. signals of unsaturated fluoro compounds in C6F6 and C6H6 show excess high field shifts corresponding to the term σc (solvent shift caused by chemical interactions). The mechanism of this shift is discussed in connection with the presence of an F-π interaction. A thermal study also supports this idea.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular secondary ion mass spectra of three pentasaccharides, viridopentaoses A, B and C, using various matrices, are discussed. The appearance of the molecular ion species is dependent upon the relative proton affinities between the sample and the organic matrix material. However, the presence of sodium ion, rather than proton, also greatly influences the appearance of the molecular ion species. The glycosidic linkages are mainly cleaved between the glycosidic oxygen atom and the anomeric carbon atom to give informative sugar sequence ions. These fragmentations have been confirmed by the linked scanning technique (B/E).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1991), S. 493-497 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A sensitive and rapid method to analyse fuel components in blood from rats exposed to kerosene or light oil vapour was developed by making use of capillary gas chromatography/mass spectrometry. The aliphatic hydrocarbons with carbon numbers 8-10 and aromatics such as toluene, xylene, 3- and 4-ethyltoluene and trimethylbenzenes were clearly detected in blood from rats exposed to kerosene or light oil vapour, using the head-space method combined with the salting-out technique. The concentration ratio of pseudocumene to toluene in blood exposed to light oil was higher than that in the case of exposure to kerosene. The lower limits of detection were 50 pg and 1 ng in toluene and pseudocumene, respectively. Our suggestion is that this method is useful in forensic investigations to detect fuel components in blood and for the purposes of differentiating kerosene and light oil in blood tissues.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 26 (1995), S. 107-112 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectra of 14 positional isomers of carboxylic acids esters with 17 skeletal atoms, CH3(CH2)m-1COO(CH2)n-1CH3(CmCOOCn) with m + n = 15 and m = 1 - 14, have been measured in the crystalline state at liquid nitrogen temperature. The relationship between the observed wavenumbers of the characteristic bands and the positions of the  - C(=O) - O -  group in the molecular chain was examined. All of the positional isomers of CmCOOCn with m + n = 15 exhibit a strong LAM-1 band in the region between 147 and 136 cm-1. The LAM-1 wavenumbers for the isomers which have the  - C(=O) - O -  group almost in the middle of the molecular chain are slightly higher (147 - 143 cm-1) than those for the isomers which have the same group almost at the end of the chain. In order to elucidate the observed LAM-1 wavenumbers, the Raman spectra of two homologous series of esters, C5COOCn and C6COOCn, were examined. All isomers of CmCOOCn give a strong band at about 1135 cm-1 assignable to the k = 1 mode of the C - C stretching vibrations. Some of the isomers give an additional k = 1 band at about 1125 cm-1. The isomers of CmCOOCn, which exhibit the two k = 1 bands, have the  - C(=O) - O -  group almost in the middle of the molecular chain, and appear to give the LAM-1 band at the higher wavenumbers. In the crystalline state all of the esters examined take the all-trans conformation with the  - C(=O) - O -  group part incorporated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 11 (1981), S. 108-111 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman band of the ν1 vibrational mode of SO42- has been measured in aqueous solutions of Na2SO4 and (NH4)2SO4 at 5-80°C, and analysed from the stochastic point of view. The band shape is approximately symmetric, but cannot be reproduced by a Lorentzian curve. The vibrational relaxation is caused by a random modulation of very low frequency from surrounding water. The vibrational correlation time for the ions is not sufficiently long to make allowance for the Markovian process of relaxation, compared with the correlation time for the bath, that is water. The vibrational correlation function appropriate for these ions is proposed.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 6 (1977), S. 89-91 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ν1 Raman linewidths of SO42- in NH4HSO4, NH4HSO4 + HCl and H2SO4 aqueous solutions were estimated by resolving the observed bands into several components with a Voigt profile. From their concentration dependence, the rate constants of proton transfer were estimated to be 4.5 × 1011 M-1s-1 consistently for the three kinds of acidic solutions.
    Additional Material: 4 Ill.
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  • 10
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The isotropic and anisotropic Raman band widths of the totally symmetric vibrations of halogen-substituted methanes have been measured in the liquid state at room temperature. The isotropic C—H and C—D stretching vibration bands broaden with increasing molecular weight and this is qualitatively explained by the Fischer-Laubereau dephasing model. The isotropic band widths of the deformation vibrations are correlated with the reorientational correlation times and are attributed to broadening due to interactions dependent on the orientation, such as the dipole-dipole interaction.
    Additional Material: 3 Ill.
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