1,890 research outputs found
Influence of Magnetic Moment Formation on the Conductance of Coupled Quantum Wires
In this report, we develop a model for the resonant interaction between a
pair of coupled quantum wires, under conditions where self-consistent effects
lead to the formation of a local magnetic moment in one of the wires. Our
analysis is motivated by the experimental results of Morimoto et al. [Appl.
Phys. Lett. \bf{82}, 3952 (2003)], who showed that the conductance of one of
the quantum wires exhibits a resonant peak at low temperatures, whenever the
other wire is swept into the regime where local-moment formation is expected.
In order to account for these observations, we develop a theoretical model for
the inter-wire interaction that calculated the transmission properties of one
(the fixed) wire when the device potential is modified by the presence of an
extra scattering term, arising from the presence of the local moment in the
swept wire. To determine the transmission coefficients in this system, we
derive equations describing the dynamics of electrons in the swept and fixed
wires of the coupled-wire geometry. Our analysis clearly shows that the
observation of a resonant peak in the conductance of the fixed wire is
correlated to the appearance of additional structure (near or
) in the conductance of the swept wire, in agreement with the
experimental results of Morimoto et al
Measurement of parity-nonconserving rotation of neutron spin in the 0.734-eV p-wave resonance of
The parity nonconserving spin rotation of neutrons in the 0.734-eV p-wave
resonance of was measured with the neutron transmission method. Two
optically polarized cells were used before and behind a a 5-cm long
target as a polarizer and an analyzer of neutron spin. The rotation
angle was carefully measured by flipping the direction of polarization
in the polarizer in sequence. The peak-to-peak value of the spin rotation was
found to be rad/cm which was consistent with
the previous experiments. But the result was statisticallly improved. The s-p
mixing model gives the weak matrix element as meV. The
value agrees well with the one deduced from the parity-nonconserving
longitudinal asymmetry in the same resonance
Soft spin waves in the low temperature thermodynamics of Pr_{0.7}Ca_{0.3}MnO_{3}
We present a detailed magnetothermal study of Pr(0.7)Ca(0.3)MnO(3), a
perovskite manganite in which an insulator-metal transition can be driven by
magnetic field, but also by pressure, visible light, x-rays, or high currents.
We find that the field-induced transition is associated with an enormous
release of energy which accounts for its strong irreversibility. In the
ferromagnetic metallic state, specific heat and magnetization measurements
indicate a much smaller spin wave stiffness than that seen in any other
manganite, which we attribute to spin waves among the ferromagnetically ordered
Pr moments. The coupling between the Pr and Mn spins may also provide a basis
for understanding the low temperature phase diagram of this most unusual
manganite.Comment: 10 pages, LATEX, 5 PDF figures, corrected typo
M153R Mutation in a pH-Sensitive Green Fluorescent Protein Stabilizes Its Fusion Proteins
BACKGROUND: Green fluorescent protein (GFP) and its fusion proteins have been used extensively to monitor and analyze a wide range of biological processes. However, proteolytic cleavage often removes GFP from its fusion proteins, not only causing a poor signal-to-noise ratio of the fluorescent images but also leading to wrong interpretations. METHODOLOGY/PRINCIPAL FINDINGS: Here, we report that the M153R mutation in a ratiometric pH-sensitive GFP, pHluorin, significantly stabilizes its fusion products while the mutant protein still retaining a marked pH dependence of 410/470 nm excitation ratio of fluorescence intensity. The M153R mutation increases the brightness in vivo but does not affect the 410/470-nm excitation ratios at various pH values. CONCLUSIONS/SIGNIFICANCE: Since the pHluorin(M153R) probe can be directly fused to the target proteins, we suggest that it will be a potentially powerful tool for the measurement of local pH in living cells as well as for the analysis of subcellular localization of target proteins
Search for the decay
We performed a search for the decay with the
E391a detector at KEK. In the data accumulated in 2005, no event was observed
in the signal region. Based on the assumption of
proceeding via parity-violation, we obtained the single event sensitivity to be
, and set an upper limit on the branching ratio to
be at the 90% confidence level. This is a factor of 3.2
improvement compared to the previous results. The results of proceeding via parity-conservation were also presented in this paper
Experimental study of the decay
The first dedicated search for the rare neutral-kaon decay
has been carried out in the E391a experiment at the
KEK 12-GeV proton synchrotron. The final upper limit of 2.6 at
the 90% confidence level was set on the branching ratio for the decay.Comment: 23 pages, 27 figures, accepted for publication as a regular article
in Physical Review
Bulk and surface switching in Mn-Fe-based Prussian Blue Analogues
Many Prussian Blue Analogues are known to show a thermally induced phase
transition close to room temperature and a reversible, photo-induced phase
transition at low temperatures. This work reports on magnetic measurements,
X-ray photoemission and Raman spectroscopy on a particular class of these
molecular heterobimetallic systems, specifically on
Rb0.81Mn[Fe(CN)6]0.95_1.24H2O, Rb0.97Mn[Fe(CN)6]0.98_1.03H2O and
Rb0.70Cu0.22Mn0.78[Fe(CN)6]0.86_2.05H2O, to investigate these transition
phenomena both in the bulk of the material and at the sample surface. Results
indicate a high degree of charge transfer in the bulk, while a substantially
reduced conversion is found at the sample surface, even in case of a near
perfect (Rb:Mn:Fe=1:1:1) stoichiometry. Thus, the intrinsic incompleteness of
the charge transfer transition in these materials is found to be primarily due
to surface reconstruction. Substitution of a large fraction of charge transfer
active Mn ions by charge transfer inactive Cu ions leads to a proportional
conversion reduction with respect to the maximum conversion that is still
stoichiometrically possible and shows the charge transfer capability of metal
centers to be quite robust upon inclusion of a neighboring impurity.
Additionally, a 532 nm photo-induced metastable state, reminiscent of the high
temperature Fe(III)Mn(II) ground state, is found at temperatures 50-100 K. The
efficiency of photo-excitation to the metastable state is found to be maximized
around 90 K. The photo-induced state is observed to relax to the low
temperature Fe(II)Mn(III) ground state at a temperature of approximately 123 K.Comment: 12 pages, 8 figure
Dizajniranje i sinteza novih derivata tiofenkarbohidrazida, tienopirazola i tienopirimidina s antioksidativnim i antitumorskim djelovanjem
2-Amino-5-acetyl-4-methyl-thiophene-3-carboxylic acid ethyl ester (1) and 5-acetyl-2-amino-4-methylthiophene-3-carbohydrazide (2) were synthesized and used as starting materials for the synthesis of new series of 1-(5-amino-4-(3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3a), 1-(5-amino-4-(4-chloro-3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3b), 1-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl) pyrazolidine-3,5-dione (4), (Z)-N\u27-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl) formohydrazonic acid (5a), (Z)-ethyl-N\u27-(4-methyl-2-amino-5-acetylthiophene-3-carbonylformo hydrazonate (5b), 6-acetyl-3-amino-2,5-dimethylthieno2,3-dpyrimidin-4(3H)-one (8), 5-methyl-3-amino-2-mercapto-6-acetylthieno2,3-dpyrimidin-4(3H)-one (10) and 5-methyl-6-acetyl-2-thioxo-2,3-dihydrothieno2,3-dpyrimidin-4(1H)-one (12) as potential antioxidant and antitumor agents. Pharmacological results showed that compounds 6a, 6b, 8, 10 and 12 exhibited promising antitumor and antioxidant activity.Etilni ester 2-amino-5-acetil-4-metil-tiofen-3-karboksilne kiseline (1) i 5-acetil-2-amino-4-metiltiofen-3-karbohidrazid (2) sintetizirani su i upotrebljeni kao reaktanti u sintezi novih spojeva 1-(5-amino-4-(3,5-dimetil-1H-pirazol-1-karbonil)-3-metiltiofen-2-il) etanona (3a), 1-(5-amino-4-(4-klor-3,5-dimetil-1H-pirazol-1-karbonil)-3-metiltiofen-2-il) etanona (3b), 1-(4-metil-2-amino-5-acetiltiofen-3-karbonil) pirazolidin-3,5-diona (4), (Z)-N\u27-(4-metil-2-amino-5-acetiltiofen-3-karbonil) formohidrazonske kiseline (5a), (Z)-etil-N\u27-(4-metil-2-amino-5-acetiltiofen-3-karbonilformo hidrazonata (5b), 6-acetil-3-amino-2,5-dimetiltieno2,3-dpirimidin-4(3H)-one (8), 5-metil-3-amino-2-merkapto-6-acetiltieno2,3-dpirimidin-4(3H)-ona (10) i 5-metil-6-acetil-2-tiokso-2,3-dihidrotieno2,3-dpirimidin-4(1H)-ona (12) kao potencijalnih antioksidansa i citostatika. Farmakološka ispitivanja ukazuju na to da spojevi 6a, 6b, 8, 10 i 12 imaju značajno antitumorsko i antioksidativno djelovanje
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