The stepwise increase of the burning voltage of short break arcs has been found not only in a gas but also in vacuum. It is suggested that the effect is associated with the occurrence of a positive anode fall which enhances ionisation phenomena near the anode. This view is supported by the simultaneous registration of arc current, burning voltage, light emission from the anode region, of spectral lines of ions, atoms and continuum from the near anode plasma. The phenomena occur beyond a critical gap distance which can be related to the characteristic geometry of the discharge. 相似文献
In this article we focus on the multiplicities of resonances, ratios of resonant over non-resonant states and rescattering processes in heavy ion collisions. Therefore we utilize a hadron transport model (UrQMD v1.3). We find that rescattering of decay particles is of great importance when studying resonances in a hadronic medium. 相似文献
A comparison has been made between the spectroscopic properties of the laser dye rhodamine 6G (R6G) in mesostructured titanium dioxide (TiO(2)) and in ethanol. Steady-state excitation and emission techniques have been used to probe the dye-matrix interactions. We show that the TiO(2)-nanocomposite studied is a good host for R6G, as it allows high dye concentrations, while keeping dye molecules isolated, and preventing aggregation. Our findings have important implications in the context of solid state dye-lasers and microphotonic device applications. 相似文献
The dipole moments of 1, 6-bridged [10]-annulenes of type I (X = CH2, O, NH) and of bromo derivatives with X = CH2, O are in agreement with the previously established structure of these compounds if a partial moment of approximately 0,8 D is assigned to the non-planar π-electron system. 相似文献
The preparation of 5,6-bis((E)-chlorommethylidene)bicyclo[2.2.2]oct-2-ene ( 13 ), 2,3-bis((E)-chloromethyl idene)-5exo,6exo- and -5endo,6endo-epoxybicyclo[2.2.2] octane ( 14 and 15 ), 5,6-bis((E)-chloromethylidene)-2exo- and -2endo-bicyclo[2.2.2] octanol ( 16 and 17 ) and 5,6-bis((E)-chloromethylidene)-2-bicyclo[2.2.2]octanone ( 18 ) are described. The face selectivity (endo-face vs. exo-face attack onto the exo-cyclic diene) of their cycloadditions to tetracyanoethylene has been determined in benzene at 20°. It is 78/22, 80/20, 60/40, 68/32, 3/97 and 30/70 for 13 , 14 , 15 , 16 , 17 and 18 , respectively. 相似文献
The syntheses of 2,3,5-trimethylidenebicyclo[2.2.1]heptane ( 1 ) and 2,3,5,6,7-pentamethylidenebicyclo[2.2.2]-octane ( 2 ) are reported. The Diels-Alder additions of the diene moieties of these polyenes can be regioselective, probably because of a possible transannular interaction between the homoconjugated methylidene and s-cis-buta-diene groups. 相似文献
We present a detailed study of the magnetization reversal in perpendicularly magnetized (Pt/Co)3 multilayers with different values of the platinum interlayer thickness tPt. To study the magnetization reversal in our samples we combined measurements of relaxation curves with the direct visualization of domain structures. Magnetization reversal was dominated by domain wall propagation for tPt=1 nm and by domain nucleation for tPt=0.2 nm, while a mixed process was observed for tPt=0.8 nm. We interpret our results within the framework of a model of thermally activated reversal where a distribution of activation energy barriers is taken into account. The reversal process was correlated with the energy barrier distribution. 相似文献