Molecular orbital momentum distributions and binding energies for nitric oxide

Binding energy spectra of the valence electrons of the open shell molecule NO have been obtained up to 55 eV at azimuthal angles of 0° and 7° using binary (e, 2e) spectroscopy at an impact energy of 1200 eV. The momentum distribution has been obtained for the least tightly bound (unpaired) electron, removal of which leads to formation of the X ¹Σ⁺ ground state of NO⁺. Momentum distributions have also been measured at 21.0 and 40.5 eV. The measured momentum distributions are compared with several literature wavefunctions of varying complexity. They are found to be in excellent agreement with those calculated using the natural spin orbital wavefunctions of Kouba and Ohrn.     

Einstein vacuum field equations with a single non-null Killing vector

It is shown that, in the case where there is a single non-null Killing vector, the vacuum Einstein field equations imply that there is a Ricci collineation in the quotient 3-space. Using coordinates adapted to the collineation vector, we derive a fourth order partial differential equation involving the metric of the quotient 3-space and we show that if this equation is satisfied, the Ernst potential may be obtained by integrating a total Riccati equation and a straightforward set of total differential equations. We also show that if the collineation vector is null, the metric of the quotient 3-space may be expressed in terms of two real Clebsch potentials. Finally in the special case where the collineation vector is the generator of a timelike homothetic motion we reduce the field equations to a single second order partial differential equation of non-Painlevé type in two independent variables and obtain Petrov type III solution of Robinson-Trautman type.     

Pro-torus actions on Poincaré duality spaces

In this paper, it is shown that some of the results of torus actions on Poincaré duality spaces, Borel’s dimension formula and topological splitting principle to local weights, hold if ‘torus’ is replaced by ‘pro-torus’.     

Growth Behavior of CdS Nanoparticles Embedded in Polymer and Sol-Gel Silica Matrices: Relationship with Surface-State Related Luminescence

Chemical techniques were employed to synthesize CdS nanoparticles embedded in polymer (PEG 300) and sol-gel silica matrices. Systematic growth of particles (radius 3–9 nm) was obtained by adjusting post-deposition annealing temperature and time to examine the dependence of surface-state–related luminescence on particle size. Photoluminescence (PL) peak energy showed a linear dependence with a gentle slope in the weak confinement region and a steep slope in the strong confinement region, the divergence being observed near the excitonic Bohr radius for CdS. The empirical relation proposed for the weak confinement region could be used for estimating chemically prepared CdS nanoparticle size with a high degree of reliability from PL peak energy.     

圆形区域内香枞芽虫的分布模型

本文讨论圆形区域内芽虫分布模型,特别研究了芽虫与天敌接触时产生与避免outbreak状态的可能性。     

Anisotropic field of background internal waves on a sea shelf and its effect on low-frequency sound propagation

The space-time spectral characteristics of the field of background internal waves (IW) are obtained for two oceanic shelf regions (the Atlantic shelf of the United States and the Kamchatka shelf) and analyzed. Within the framework of a numerical experiment, it is shown that the observed anisotropy of the IW field may considerably affect the low-frequency sound fluctuations in the aforementioned regions and, in particular, may change the interference invariant of the sound field.     

Photochemically generated carotenoid radicals on Nafion film and silica gel: an EPR and ENDOR study

Carotenoid cation radicals have been observed at 120 K, by EPR and proton ENDOR measurements, to be formed upon 77 K photolysis of thin films of Nafion or silica gel coated with the carotenoids, β-carotene and canthaxanthin. The powder ENDOR spectra consist of resolvable lines due to couplings larger than 2.8 MHz but smaller than 17 MHz assigned to the methyl protons of the carotenoid cation radical and to an -proton of the planar polyene chain.