8,460 research outputs found

    On the sine-Gordon--Thirring equivalence in the presence of a boundary

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    In this paper, the relationship between the sine-Gordon model with an integrable boundary condition and the Thirring model with boundary is discussed and the reflection RR-matrix for the massive Thirring model, which is related to the physical boundary parameters of the sine-Gordon model, is given. The relationship between the the boundary parameters and the two formal parameters appearing in the work of Ghoshal and Zamolodchikov is discussed.Comment: 14 pages, Latex, to be published in Int. J. Mod. Phys. A. Two references adde

    Modes of zonal mean temperature variability 20–100 km from the TIMED/SABER observations

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    In this study we investigate the spatial variabilities of the zonal mean temperature (20–100 km) from the TIMED (Thermosphere, Ionosphere, Mesosphere, Energetics and Dynamics)/SABER (Sounding of the Atmosphere using Broadband Emission Radiometry) satellite using the empirical orthogonal functions (EOFs). After removing the climatological annual mean, the first three EOFs are able to explain 87.0% of temperature variabilities. The primary EOF represents 74.1% of total anomalies and is dominated by the north–south contrast. Patterns in the second and third EOFs are related to the semiannual oscillations (SAO) and mesospheric temperature inversions (MTI), respectively. The quasi-biennial oscillation (QBO) component is also decomposed into the seventh EOF with contributions of 1.2%. Last, we use the first three modes and annual mean temperature to reconstruct the data. The result shows small differences are in low latitude, which increase with latitude in the middle stratosphere and upper mesosphere

    Phase diagram of the frustrated, spatially anisotropic S=1 antiferromagnet on a square lattice

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    We study the S=1 square lattice Heisenberg antiferromagnet with spatially anisotropic nearest neighbor couplings J1xJ_{1x}, J1yJ_{1y} frustrated by a next-nearest neighbor coupling J2J_{2} numerically using the density-matrix renormalization group (DMRG) method and analytically employing the Schwinger-Boson mean-field theory (SBMFT). Up to relatively strong values of the anisotropy, within both methods we find quantum fluctuations to stabilize the N\'{e}el ordered state above the classically stable region. Whereas SBMFT suggests a fluctuation-induced first order transition between the N\'{e}el state and a stripe antiferromagnet for 1/3≤J1x/J1y≤11/3\leq J_{1x}/J_{1y}\leq 1 and an intermediate paramagnetic region opening only for very strong anisotropy, the DMRG results clearly demonstrate that the two magnetically ordered phases are separated by a quantum disordered region for all values of the anisotropy with the remarkable implication that the quantum paramagnetic phase of the spatially isotropic J1J_{1}-J2J_{2} model is continuously connected to the limit of decoupled Haldane spin chains. Our findings indicate that for S=1 quantum fluctuations in strongly frustrated antiferromagnets are crucial and not correctly treated on the semiclassical level.Comment: 10 pages, 10 figure

    Synthesis, characterization and crystal structure of a dioxomolybdenum(VI) complex derived from N’-(2-hydroxy-4-diethaylaminobenzylidene)-4-hydroxybenzohydrazide

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    Reaction of [MoO2(acac)2] (where acac = acetylacetonate) with N’-(2-hydroxy-4-diethaylaminobenzylidene)-4-hydroxybenzohydrazide (H2L) in methanol afforded a methanol-coordinated mononuclear molybdenum(VI) oxo complex, [MoO2L(MeOH)]. Crystal and molecular structure of the complex were determined by single crystal X-ray diffraction method. The complex was further characterized by elemental analysis and FT-IR spectra. Single crystal X-ray structural studies indicate that the hydrazone ligand coordinates to the MoO2 core through enolate oxygen, phenolate oxygen and azomethine nitrogen. The Mo atom in the complex is in octahedral coordination. Thermal stability of the complex has also been studied. KEY WORDS: Molybdenum complex, Hydrazone ligand, Crystal structure, X-ray diffraction, Thermal property Bull. Chem. Soc. Ethiop. 2014, 28(3), 409-414.DOI: http://dx.doi.org/10.4314/bcse.v28i3.1
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