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1.
A. Maignan Ch. Simon V. Caignaert B. Raveau 《Zeitschrift für Physik B Condensed Matter》1995,99(1):305-310
The exploration of the magnetic and transport properties of four series of manganese perovskites, Pr0.7Ca0.34−xAxMnO3−δ (A=Sr, Ba), Pr0.7−xLaxCa0.3 MnO3−δ and Pr0.66Ca0.34−x
SrxMnO3−δ has allowed four phases with colossal magnetoresistive (CMR) properties to be isolated: Pr0.7Ca0.25Sr0.025MnO3−δ and Pr0.66Ca0.26Sr0.08MnO3−δ that exhibit a variation of resistance of 2.5. 107% and 109% at μ0 H=5 T for T=88 K and 50 K respectively, Pr0.58La0.12Ca0.3 MnO3−δ that exhibits a variation of 6.106% for μ0 H=5 T at T=80 K and Pr0.7Ba0.025Ca0.275MnO3−δ for which a resistance variation of 5.109%, at T=50 K, for μ0 H=5 T is evidenced. for each compound of this series except the barium phase, one observes that the temperature Tmax, which corresponds to the resistance maximum on the R(T) curves in zero magnetic field, increases dramatically as the mean
size of the interpolated cations increases, and that the CMR effect correlatively decreases dramatically. The comparison of
the two series Pr0.7Ca0.3−xSrxMnO3−δ and Pr0.66Ca0.34−xSrxMnO3−δ shows also the crucial role of the hole carrier density: for a same mean ionic radius of the interpolated cation Tmax is decreased of about 50 K by introducing 0.034 hole per Mn mole. 相似文献
2.
A. Barnabé A. Maignan M. Hervieu B. Raveau 《The European Physical Journal B - Condensed Matter and Complex Systems》1998,1(2):145-150
Doping of Mn-site by chromium, cobalt and nickel has been investigated in the calcium rich manganites and
. Whatever the nature of the doping element, a rapid disappearance of the charge ordered (CO) state is observed, decreasing as the doping rate increases. But the most important result concerns the Cr-doped compounds for which a re-entrant insulator to metal transition at 90-120 K is observed for x
=0.10-0.12, in a zero magnetic field. The possibility to induce colossal magnetoresistance (CMR) properties for high (IV) contents ((IV)/) for x
=0.07-0.12 is shown for the first time, the resistance ratios reaching at 30 K. This study also shows differently that the small size of the A-site cation (Pr, Ca) is not a redhibitory obstacle
to the appearance of CMR properties in manganites, in contrast with previously established phase diagrams.
Received: 18 June 1997 / Revised: 4 August 1997 / Accepted: 10 November 1997 相似文献
3.
4.
Ba(2)CoS(3) is the first example of an inorganic solid containing one-dimensional corner-sharing [Co(2+)-anion] chains, which leads to one-dimensional cooperative antiferromagnetism. 相似文献
5.
Marine de Person Aude Sevestre P. Chaimbault Laurent Perrot Francis Duchiron Claire Elfakir 《Analytica chimica acta》2004,520(1-2):149-158
This paper reports the use of an on-line LC–ESI–MS/MS method for the identification and quantification of di- and tripeptides in champagne wine without laborious sample pretreatment. The identification of these compounds, in their underivatised form, is based on identical retention times and ESI–MS spectra to those of reference standards. The presence of nine dipeptides (Arg–Ile, Ile–Arg, Ile–Val, Lys–Phe, Lys–Tyr, Phe–Lys, Tyr–Gln, Tyr–Lys, Val–Ile) and the absence of two tripeptides (Phe–Arg–Arg and Lys–Met–Asn) have been evidenced in the matrix. Calibration curves for each analyte were established using Phe–Arg as internal standard. The calibration curves were linear in the concentration range 0.1–10 mg L−1 with a determination coefficient, r2, better than 0.992. The accuracy for the calibration standard was estimated at between 92 and 102%. This method allows high recovery and satisfies the necessary requirements with respect to accuracy, repeatability and sensitivity. The first application of this analytical method to the measurement of di- and tri-peptides in different vintages of champagne wine is reported. Compositional changes in the peptides occurred depending on the vintage. 相似文献
6.
Sylvie Malo Antoine Maignan Sylvain Marinel Maryvonne Hervieu Kenneth R. Poeppelmeier Bernard Raveau 《Solid State Sciences》2005,7(12):1492
Recently, the ferroelectromagnet YMnO3 has been the focus of interest because it exhibits both antiferromagnetism (Néel temperature 80 K) and ferroelectricity (Curie temperature 914 K). There have been no reports of complete YMn1−xMxO3 solid solutions in which substitution of the foreign M cation preserves the hexagonal P63cm structure. In contrast there exist several homeotypic phases with the general formula, Ln1+nCunMO3+3n (n=1 (M=Ti), 2 (M=V) and 3 (M=Mo); Ln: lanthanide). Several YMn1−x(Cu3/4Mo1/4)xO3 compounds have been synthesized. The solid solution, from YMnO3 (x=0) to YCu3/4Mo1/4O3 (x=1) has been characterized by X-ray diffraction and transmission electron microscopy study. For 0<x<0.9, the compounds are found to crystallize in the non-centrosymmetric structure, space group P63cm, of YMnO3. The Mn-free end member, x=1, crystallizes in a complex multiple cell, the superstructure being associated to Cu3+/Mo6+ cationic ordering. Dilution of the Mn3+ magnetic array by the paramagnetic (Cu2+) and diamagnetic (Mo6+) cations is found to decrease the antiferromagnetic ordering temperature and it becomes undetectable for x0.5 compositions. 相似文献
7.
C. Yaicle F. Fauth R. Retoux M. Hervieu A. Maignan 《Journal of solid state chemistry》2005,178(5):1652-1660
Combining low-temperature electron (ED) and synchrotron powder diffraction (SPD) techniques, we have precisely determined the phase-separated crystal structure of Pr0.5Ca0.5Mn0.97Ga0.03O3. We demonstrate that the phase separation is associated with the onset of charge/orbital ordering at ∼230 K and that two ordered phases coexist at low temperature. In order to account for the significant anisotropic linewidth broadening observed in the SPD patterns, we had to include a specific strain model in the refinements. One of the phases, the most severely strained, is suggested to result from an imperfect charge ordering. 相似文献
8.
Aude Fayol 《Tetrahedron》2005,61(48):11511-11519
Three-component reaction of an α-isocyanoacetamide 7, an homoallylamine 8 and an aldehyde 9 in methanol at room temperature provides oxa-bridged tricycle 4 in good to excellent yield as a mixture of two separable diastereoisomers. In this one-pot multicomponent process, one C-N, one C-O and three C-C bonds are formed with concomitant creation of five asymmetric centers and three rings. Fragmentation of epoxy-tetrahydronaphthyridine 4 affords differentially substituted 5,6,7,8-tetrahydro-1,7-naphthyridine (5, 6) depending on the reaction conditions, providing thus additional structural diversity. A one-pot three-component synthesis of 5,6,7,8-tetrahydro-1,7-naphthyridine (6) from 7, 8 and 9 is also documented. 相似文献
9.
We report on an innovative configuration of a supercontinuum laser based on an Yb-doped nonlinear microstructured fiber. Due to this particular fiber design combining amplification and nonlinear properties, a wideband output spectrum is generated in the fiber under the Q-switched regime. By exploiting stimulated Brillouin scattering, high peak power pulses are achieved and contribute to a spectral broadening due to a nonlinear wavelength conversion process. Both infrared (1000-1200 nm) and visible (650-750 nm) spectra are generated with an average power of 200 mW. 相似文献
10.
Contribution of Cytosine‐Containing Cyclobutane Dimers to DNA Damage Produced by Photosensitized Triplet–Triplet Energy Transfer
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Dr. Thierry Douki Izabel Bérard Aude Wack Sigrid Andrä 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(19):5787-5794
Mutagenic cyclobutane pyrimidine dimers (CPDs) can be induced in DNA through either direct excitation or photosensitized triplet–triplet energy transfer (TTET). In the latter pathway, thymines are expected to receive the excitation energy from the photosensitizer and react with adjacent pyrimidines. By using state‐of‐the art analytical tools, we provide herein additional information on the formation of cytosine‐containing CPDs. We thus determined the yield of all possible CPDs upon TTET in a series of natural DNAs with various base compositions. We show that the distribution of CPDs cannot be explained only by excitation of individual thymines. We propose that the mechanism for TTET involves at least dinucleotides as the minimal targets. The observation of the formation of cytosine–cytosine CPDs also suggests that additional pathways are involved in this photosensitized reaction. 相似文献