123 research outputs found

    Observation of elastic anomalies driven by coexisting dynamical spin Jahn-Teller effect and dynamical molecular spin state in paramagnetic phase of the frustrated MgCr2_2O4_4$

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    Ultrasound velocity measurements of magnesium chromite spinel MgCr2_2O4_4 reveal elastic anomalies in the paramagnetic phase that are characterized as due to geometrical frustration. The temperature dependence of the tetragonal shear modulus (C11−C12)/2(C_{11}-C_{12})/2 exhibits huge Curie-type softening, which should be the precursor to spin Jahn-Teller distortion in the antiferromagnetic phase. The trigonal shear modulus C44C_{44} exhibits nonmonotonic temperature dependence with a characteristic minimum at ∌\sim50 K, indicating a coupling of the lattice to dynamical molecular spin state. These results strongly suggest the coexistence of dynamical spin Jahn-Teller effect and dynamical molecular spin state in the paramagnetic phase, which is compatible with the coexistence of magnetostructural order and dynamical molecular spin state in the antiferromagnetic phase.Comment: 6 pages, 3 figure

    Elastic Instabilities within Antiferromagnetically Ordered Phase in the Orbitally-Frustrated Spinel GeCo2_2O4_4

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    Ultrasound velocity measurements of the orbitally-frustrated GeCo2_2O4_4 reveal unusual elastic instabilities due to the phonon-spin coupling within the antiferromagnetic phase. Shear moduli exhibit anomalies arising from the coupling to short-range ferromagnetic excitations. Diplike anomalies in the magnetic-field dependence of elastic moduli reveal magnetic-field-induced orbital order-order transitions. These results strongly suggest the presence of geometrical orbital frustration which causes novel orbital phenomena within the antiferromagnetic phase.Comment: 5 pages, 3 figure

    Coulomb correlations intertwined with spin and orbital excitations in LaCoO3_3

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    We carried out temperature-dependent (20 - 550 K) measurements of resonant inelastic X-ray scattering on LaCoO3_3 to investigate the evolution of its electronic structure across the spin-state crossover. In combination with charge-transfer multiplet calculations, we accurately quantized the renormalized crystal-field excitation energies and spin-state populations. We show that the screening of the on-site Coulomb interaction of 3d electrons is orbital selective and coupled to the spin-state crossover in LaCoO3_3. The results establish that the gradual spin-state crossover is associated with a relative change of Coulomb energy versus bandwidth, leading to a Mott-type insulator-to-metal transition.Comment: 6 pages, 4 figures. Submitted to Phys. Rev. Let

    Emergence of magnetic long-range order in frustrated pyrochlore Nd2_2Ir2_2O7_7 with metal-insulator transition

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    In this study, we performed powder neutron diffraction and inelastic scattering measurements of frustrated pyrochlore Nd2_2Ir2_2O7_7, which exhibits a metal-insulator transition at a temperature TMIT_{\rm MI} of 33 K. The diffraction measurements revealed that the pyrochlore has an antiferromagnetic long-range structure with propagation vector q⃗0\vec{q}_{0} of (0,0,0) and that it grows with decreasing temperature below 15 K. This structure was analyzed to be of the all-in all-out type, consisting of highly anisotropic Nd3+^{3+} magnetic moments of magnitude 2.3±0.42.3\pm0.4ÎŒB\mu_{\rm B}, where ÎŒB\mu_{\rm B} is the Bohr magneton. The inelastic scattering measurements revealed that the Kramers ground doublet of Nd3+^{3+} splits below TMIT_{\rm MI}. This suggests the appearance of a static internal magnetic field at the Nd sites, which probably originates from a magnetic order consisting of Ir4+^{4+} magnetic moments. Here, we discuss a magnetic structure model for the Ir order and the relation of the order to the metal-insulator transition in terms of frustration.Comment: 6 pages, 1 table, 3 figure

    Magnetic Frustration Driven by Itinerancy in Spinel CoV2O4

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    Localized spins and itinerant electrons rarely coexist in geometrically-frustrated spinel lattices. They exhibit a complex interplay between localized spins and itinerant electrons. In this paper, we study the origin of the unusual spin structure of the spinel CoV2O4, which stands at the crossover from insulating to itinerant behavior using the first principle calculation and neutron diffraction measurement. In contrast to the expected paramagnetism, localized spins supported by enhanced exchange couplings are frustrated by the effects of delocalized electrons. This frustration produces a non-collinear spin state even without orbital orderings and may be responsible for macroscopic spin-glass behavior. Competing phases can be uncovered by external perturbations such as pressure or magnetic field, which enhances the frustration

    Development of Plasma Vitellogenin Assay for Estrogenic Effects of Endocrine-Disrupting Chemicals Using Ovariectomized Goldfish (Carassius auratus)

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    Plasma vitellogenin (VTG) assay was developed using ovariectomized goldfish (Carassius auratus) for determining the estrogenic effects of endocrine-disrupting chemicals. In a laboratory study, we assessed the estrogenic activity of commercial fish diets by using a diet for ornamental carp (CD) and a casein-based formulated fish diet (FD), which was shown to not contain soybean or fish meal in a previous study. In ovariectomized fish, plasma VTG concentrations were significantly higher in the CD-fed group than in the FD-fed group. These results indicate that the estrogen activity of CD may be high enough to cause induction of plasma VTG in ovariectomized goldfish as previously observed in male goldfish. Moreover, the effect of estrogen on plasma VTG induction was confirmed by significant plasma VTG production following the exposure of FD-fed ovariectomized goldfish to a nominal estradiol-17ÎČ concentration of 100 ÎŒg/l for 31 days. Our data suggest that induction of plasma VTG using ovariectomized goldfish is a good tool for evaluating the estrogenic effects of endocrine-disrupting chemicals

    An Efficient Approach to the Synthesis of Novel Pyrene-Fused Azaacenes

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    This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters (copyright © American Chemical Society) after peer review and technical editing by the publisher. To access the final edited and published work see: http://dx.doi.org/10.1021/ol401438
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