13,904 research outputs found
Constraining the Equation of State with Moment of Inertia Measurements
We estimate that the moment of inertia of star A in the recently discovered
double pulsar system PSR J0737-3039 may be determined after a few years of
observation to something like 10% accuracy. This would enable accurate
estimates of the radius of the star and the presure of matter in the vicinity
of 1 to 2 times the nuclear saturation density, which would in turn provide
strong constraints on the equation of state of neutron stars and the physics of
their interiors.Comment: Submitted to ApJ, 4 figure
Lattice results for the decay constant of heavy-light vector mesons
We compute the leptonic decay constants of heavy-light vector mesons in the
quenched approximation. The reliability of lattice computations for heavy
quarks is checked by comparing the ratio of vector to pseudoscalar decay
constant with the prediction of Heavy Quark Effective Theory in the limit of
infinitely heavy quark mass. Good agreement is found. We then calculate the
decay constant ratio for B mesons: .
We also quote quenched MeV.Comment: 11 pages, 3 postscript figs., revtex; two references adde
A Classification of random Dirac fermions
We present a detailed classification of random Dirac hamiltonians in two
spatial dimensions based on the implementation of discrete symmetries. Our
classification is slightly finer than that of random matrices, and contains
thirteen classes. We also extend this classification to non-hermitian
hamiltonians with and without Dirac structure.Comment: 15 pages, version2: typos in the table of classes are correcte
New imino-pyridyl nickel (II) complexes: synthesis, molecular structures and application as Heck coupling catalysts
Reactions of imino-pyridyl ligands, (2-pyridyl-2-thiophenemethyl)imine (L1) and (2-pyridyl-2-thiopheneethyl)imine (L2) with NiBr2(DME) gave the corresponding complexes [Ni(L1)Br2] (1) and [Ni(L2)Br2] (2) in good yields. Treatment of 1 and 2 with one equivalent of 2-hydroxythiophenol resulted in the displacement of the bromide ligands to form the nickel(II) thiolato complexes 3 and 4. Molecular structure of 3 confirmed that L1 and L2 bind to the nickel atom in a bidentate fashion. Complexes 1-4 catalyzed the Heck coupling reaction of iodobenzene and bromobenzene with methyl acrylate.Web of Scienc
Lattice Calculation of Heavy-Light Decay Constants with Two Flavors of Dynamical Quarks
We present results for , , , and their ratios in
the presence of two flavors of light sea quarks (). We use Wilson light
valence quarks and Wilson and static heavy valence quarks; the sea quarks are
simulated with staggered fermions. Additional quenched simulations with
nonperturbatively improved clover fermions allow us to improve our control of
the continuum extrapolation. For our central values the masses of the sea
quarks are not extrapolated to the physical , masses; that is, the
central values are "partially quenched." A calculation using "fat-link clover"
valence fermions is also discussed but is not included in our final results. We
find, for example,
MeV, , MeV, and , where in each case the first error is
statistical and the remaining three are systematic: the error within the
partially quenched approximation, the error due to the missing strange
sea quark and to partial quenching, and an estimate of the effects of chiral
logarithms at small quark mass. The last error, though quite significant in
decay constant ratios, appears to be smaller than has been recently suggested
by Kronfeld and Ryan, and Yamada. We emphasize, however, that as in other
lattice computations to date, the lattice quark masses are not very light
and chiral log effects may not be fully under control.Comment: Revised version includes an attempt to estimate the effects of chiral
logarithms at small quark mass; central values are unchanged but one more
systematic error has been added. Sections III E and V D are completely new;
some changes for clarity have also been made elsewhere. 82 pages; 32 figure
Measurement of the intrinsic damping constant in individual nanodisks of YIG and YIG{\textbar}Pt
We report on an experimental study on the spin-waves relaxation rate in two
series of nanodisks of diameter 300, 500 and 700~nm, patterned out of
two systems: a 20~nm thick yttrium iron garnet (YIG) film grown by pulsed laser
deposition either bare or covered by 13~nm of Pt. Using a magnetic resonance
force microscope, we measure precisely the ferromagnetic resonance linewidth of
each individual YIG and YIG{\textbar}Pt nanodisks. We find that the linewidth
in the nanostructure is sensibly smaller than the one measured in the extended
film. Analysis of the frequency dependence of the spectral linewidth indicates
that the improvement is principally due to the suppression of the inhomogeneous
part of the broadening due to geometrical confinement, suggesting that only the
homogeneous broadening contributes to the linewidth of the nanostructure. For
the bare YIG nano-disks, the broadening is associated to a damping constant
. A 3 fold increase of the linewidth is observed for
the series with Pt cap layer, attributed to the spin pumping effect. The
measured enhancement allows to extract the spin mixing conductance found to be
for our
YIG(20nm){\textbar}Pt interface, thus opening large opportunities for the
design of YIG based nanostructures with optimized magnetic losses.Comment: 4 pages, 3 figure
String Breaking in Lattice Quantum Chromodynamics
The separation of a heavy quark and antiquark pair leads to the formation of
a tube of flux, or string, which should break in the presence of light
quark-antiquark pairs. This expected zero temperature phenomenon has proven
elusive in simulations of lattice QCD. We present simulation results that show
that the string does break in the confining phase at nonzero temperature.Comment: 11 pages RevTeX, including 4 encapsulated Postscript figures.
version2: minor corrections to reference
A mechanistic modelling and data assimilation approach to estimate the carbon/chlorophyll and carbon/nitrogen ratios in a coupled hydrodynamical-biological model
The principal objective of hydrodynamical-biological models is to provide estimates of the main carbon fluxes such as total and export oceanic production. These models are nitrogen based, that is to say that the variables are expressed in terms of their nitrogen content. Moreover models are calibrated using chlorophyll data sets. Therefore carbon to chlorophyll (C:Chl) and carbon to nitrogen (C:N) ratios have to be assumed. This paper addresses the problem of the representation of these ratios. In a 1D framework at the DYFAMED station (NW Mediterranean Sea) we propose a model which enables the estimation of the basic biogeochemical fluxes and in which the spatio-temporal variability of the C:Chl and C:N ratios is fully represented in a mechanical way. This is achieved through the introduction of new state variables coming from the embedding of a phytoplankton growth model in a more classical Redfieldian NNPZD-DOM model (in which the C:N ratio is assumed to be a constant). Following this modelling step, the parameters of the model are estimated using the adjoint data assimilation method which enables the assimilation of chlorophyll and nitrate data sets collected at DYFAMED in 1997.Comparing the predictions of the new Mechanistic model with those of the classical Redfieldian NNPZD-DOM model which was calibrated with the same data sets, we find that both models reproduce the reference data in a comparable manner. Both fluxes and stocks can be equally well predicted by either model. However if the models are coinciding on an average basis, they are diverging from a variability prediction point of view. In the Mechanistic model biology adapts much faster to its environment giving rise to higher short term variations. Moreover the seasonal variability in total production differs from the Redfieldian NNPZD-DOM model to the Mechanistic model. In summer the Mechanistic model predicts higher production values in carbon unit than the Redfieldian NNPZD-DOM model. In winter the contrary holds
Synthesis, Physical and Antimicrobial Studies of Ferrocenyl-N-(pyridinylmethylene)anilines and Ferrocenyl-N-(pyridinylmethyl)anilines
Ferrocenyl-N-(pyridinylmethylene)anilines Schiff bases were synthesized by reaction of 3- or 4-ferrocenylaniline with either 2-, 3-, or 4-pyridinecarboxaldehyde under solvent-free conditions via mechanochemistry technique. Products were obtained in excellent yields within 10 min of grinding. The reactions afforded a melt orgummysemi-solid that solidified to the desired Schiff bases within a short time. These Schiff bases were reduced to their corresponding amines, ferrocenyl-N-(pyridinylmethyl)anilines, with NaBH4 over neutral Al2O3 solid support via grinding. Amines were obtained in excellent yields after intermittent grinding for approximately 1 h. Herein, five novel ferrocenyl-N-(pyridinylmethylene)anilines (compounds 3, 4, 6â8) and six ferrocenyl-N-(pyridinylmethyl)anilines (compounds 9â14) are reported. Compounds were characterized through FT-IR, 1H-NMR, 13C-NMR,HRMSand SC-XRDtechniques. These compounds show visible solvatochromism, whenUV-Vis absorption was measured in polar and nonpolar solvents. In changing solvent from polar to non-polar, the Schiff bases exhibited a blue shift while the amines portrayed a red shift. Electrochemical studies on these compounds reveal that redox behaviour of the iron centre is influenced by the position imine or amine groups. Antimicrobial properties of these compounds were studied for Escherichia coli, Staphylococcus aureus, Salmonella typhimirium and Candida albicans. Highest activity was recorded against Gram-positive bacteria and fungi.KEYWORDS Ferrocenyl-N-(pyridinylmethylene)anilines, ferrocenyl-N-(pyridinylmethyl)anilines, mechanochemistry technique, solventfree synthesis, antimicrobial activity
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