254 research outputs found
The nature of the progenitor of the M31 north-western stream: globular clusters as milestones of its orbit
We examine the nature, possible orbits and physical properties of the progenitor of the north-western stellar stream (NWS) in the halo of the Andromeda galaxy (M31). The progenitor is assumed to be an accreting dwarf galaxy with globular clusters (GCs). It is, in general, difficult to determine the progenitor\u27s orbit precisely because of many necessary parameters. Recently, Veljanoski et al. reported five GCs whose positions and radial velocities suggest an association with the stream. We use these data to constrain the orbital motions of the progenitor using test-particle simulations. Our simulations split the orbit solutions into two branches according to whether the stream ends up in the foreground or in the background of M31. Upcoming observations that will determine the distance to the NWS will be able to reject one of the two branches. In either case, the solutions require that the pericentric radius of any possible orbit be over 2 kpc. We estimate the efficiency of the tidal disruption and confirm the consistency with the assumption for the progenitor being a dwarf galaxy. The progenitor requires the mass ≳ 2 × 106 M⊙ and half-light radius ≳ 30 pc. In addition, N-body simulations successfully reproduce the basic observed features of the NWS and the GCs\u27 line-of-sight velocities
Bonding Nature in MgB2
The accurate charge density of MgB2 was observed at room temperature(R.T.)
and 15K by the MEM(Maximum Entropy Method)/Rietveld analysis using synchrotron
radiation powder data. The obtained charge density clearly revealed the
covalent bonding feature of boron forming the 2D honeycomb network in the basal
plane, on the other hand, Mg is found to be in divalent state. A subtle but
clear charge concentration was found on boron 2D sheets at 15K, which should be
relating to superconductivity.Comment: 4 pages, 3 figure
Mechanisms of toxic action and structure-activity relationships for organochlorine and synthetic pyrethroid insecticides.
The mechanisms and sites of action of organochlorine (DDT-types and chlorinated alicyclics) and synthetic pyrethroid insecticides are presented with discussion of symptoms, physiological effects, and selectivity. The structural requirements for toxicity are assessed, and structure-activity relationships are considered for each subclass. Lipophilicity is important for all the groups because it facilitates delivery of these neurotoxicants to the site of action in the nerve. Steric factors including molecular volume, shape, and isomeric configuration greatly influence toxicity. Electronic parameters also have been demonstrated to affect biological activity in some of the groups of insecticides, e.g., Hammett's sigma and Taft's sigma * as indicators of electronegativity. New synthetic pyrethroids continue to be developed, with varied structures and different physicochemical and biological properties
Thermoelectric Signal Enhancement by Reconciling the Spin Seebeck and Anomalous Nernst Effects in Ferromagnet/Non-magnet Multilayers
The utilization of ferromagnetic (FM) materials in thermoelectric devices allows one to have a simpler structure and/or independent control of electric and thermal conductivities, which may further remove obstacles for this technology to be realized. The thermoelectricity in FM/non-magnet (NM) heterostructures using an optical heating source is studied as a function of NM materials and a number of multilayers. It is observed that the overall thermoelectric signal in those structures which is contributed by spin Seebeck effect and anomalous Nernst effect (ANE) is enhanced by a proper selection of NM materials with a spin Hall angle that matches to the sign of the ANE. Moreover, by an increase of the number of multilayer, the thermoelectric voltage is enlarged further and the device resistance is reduced, simultaneously. The experimental observation of the improvement of thermoelectric properties may pave the way for the realization of magnetic-(or spin-) based thermoelectric devicesopen4
Oxidation of benzoin catalyzed by oxovanadium (IV) schiff base complexes
BACKGROUND: The oxidative transformation of benzoin to benzil has been accomplished by the use of a wide
variety of reagents or catalysts and different reaction procedures. The conventional oxidizing agents yielded mainly
benzaldehyde or/and benzoic acid and only a trace amount of benzil. The limits of practical utilization of these
reagents involves the use of stoichiometric amounts of corrosive acids or toxic metallic reagents, which in turn
produce undesirable waste materials and required high reaction temperatures.
In recent years, vanadium complexes have attracted much attention for their potential utility as catalysts for various
types of reactions.
RESULTS: Active and selective catalytic systems of new unsymmetrical oxovanadium(IV) Schiff base complexes for
the oxidation of benzoin is reported. The Schiff base ligands are derived between 2-aminoethanol and 2-hydroxy-1-
naphthaldehyde (H2L1) or 3-ethoxy salicylaldehyde (H2L3); and 2-aminophenol and 3-ethoxysalicylaldehyde (H2L2) or
2-hydroxy-1-naphthaldehyde (H2L4). The unsymmetrical Schiff bases behave as tridentate dibasic ONO donor
ligands. Reaction of these Schiff base ligands with oxovanadyl sulphate afforded the mononuclear oxovanadium(IV)
complexes (VIVOLx.H2O), which are characterized by various physico-chemical techniques.
The catalytic oxidation activities of these complexes for benzoin were evaluated using H2O2 as an oxidant. The best
reaction conditions are obtained by considering the effect of solvent, reaction time and temperature. Under the
optimized reaction conditions, VOL4 catalyst showed high conversion (>99%) with excellent selectivity to benzil
(~100%) in a shorter reaction time compared to the other catalysts considered.
CONCLUSION: Four tridentate ONO type Schiff base ligands were synthesized. Complexation of these ligands with
vanadyl(IV) sulphate leads to the formation of new oxovanadium(IV) complexes of type VIVOL.H2O.
Elemental analyses and spectral data of the free ligands and their oxovanadium(IV) complexes were found to be in
good agreement with their structures, indicating high purity of all the compounds.
Oxovanadium complexes were screened for the oxidation of benzoin to benzil using H2O2 as oxidant. The effect of
time, solvent and temperature were optimized to obtain maximum yield. The catalytic activity results demonstrate
that these catalytic systems are both highly active and selective for the oxidation of benzoin under mild reaction
conditions.Web of Scienc
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