Nucleon Mass Splitting at Finite Isospin Chemical Potential

We investigate nucleon mass splitting at finite isospin chemical potential in the frame of two flavor Nambu--Jona-Lasinio model. It is analytically proved that, in the phase with explicit isospin symmetry breaking the proton mass decreases and the neutron mass increases linearly in the isospin chemical potential.Comment: 3 pages and no figure

Tunable synchrotron-like radiation from centimeter scale plasma channels

Synchrotron radiation sources are immensely useful tools for scientific researches and many practical applications. Currently, the state-of-the-art synchrotrons rely on conventional accelerators, where electrons are accelerated in a straight line and radiate in bending magnets or other insertion devices. However, these facilities are usually large and costly. Here, we study a compact all-optical synchrotron like radiation source based on laser-plasma acceleration either in a straight or a curved plasma channel. With the laser pulse off-axially injected, its centroid oscillates transversely in the plasma channel. This results in a wiggler motion of the whole accelerating structure and the self-trapped electrons behind the laser pulse, leading to strong synchrotron-like radiations with tunable spectra. It is further shown that a palmtop ring-shaped synchrotron is possible with current high power laser technologies. With its potential of high flexibility and tunability, such light sources once realized would find applications in wide areas and make up the shortage of large synchrotron radiation facilities

Tris(1,10-phenanthroline-κ2 N,N′)zinc(II) chloride 2-phenyl-4-selenazole-5-car­box­yl­ate decahydrate

The asymmetric unit of the title salt, [Zn(C12H8N2)3](C10H6NO2Se)Cl·10H2O, contains a [Zn(phen)3]2+ cation (phen is 1,10-phenanthroline), uncoordinated chloride and 2-phenyl-4-selenazole-5-carboxyl­ate anions and ten uncoord­in­ated water mol­ecules. The central ZnII ion is six-coordinated by six N atoms from three phen ligands in a distorted octa­hedral geometry. An extensive O—H⋯O, O—H⋯N and O—H⋯Cl hydrogen-bonding network stabilizes the crystal structure

Aqua­[2-(5-ethyl-2-pyridyl-κN)-4-iso­propyl-4-methyl-5-oxo-4,5-dihydroxy­imidazol-1-ido-κN 1](5-methyl-1H-pyrazole-3-carboxyl­ato-κ2 N 2,O)copper(II) 1.33-hydrate

In the title complex, [Cu(C5H5N2O2)(C14H18N3O)(H2O)]·1.33H2O, the CuII ion is coordinated in a slightly distorted square-pyramidal environment. The basal plane is formed by two N atoms from a 2-(5-ethyl-2-pyridyl-κN)-4-isopropyl-4-methyl-5-oxo-4,5-dihydroxy­imidazol-1-ide ligand and by one O atom and one N atom from a 5-methyl-1H-pyrazole-3-carboxyl­ate ligand. The apical position is occupied by a water mol­ecule. In the crystal structure, O—H⋯O, O—H⋯N and N—H⋯O hydrogen bonds lead to a three-dimensional supra­molecular network