Frequency stability of an optically pumped cesium beam frequency standard

Results obtained in an experimental optically pumped cesium beam frequency standard in which a single semiconductor laser is used for the state selection and the atom detection are reported. The separation between the two interaction regions is equal to 21 cm. This gives a 500 Hz linewidth which is observed with a signal to noise ratio equal to 10,000 in a 1 Hz noise bandwidth. A quartz crystal oscillator is frequency controlled by the atomic transition. The measured short term frequency stability is given by _y()=2×10^–12–1/2 for 1 s<500 s. Prospects for improvement of this frequency stability are discussed.     

Spectroscopic investigation of the ionization kinetics in XeCl laser discharges by Xe* density measurements

Time and spatially resolved absorption measurements of Xe^* particle number densities performed at an X-ray preionized self-sustained XeCl^*-laser discharge were used to investigate the reaction kinetics of such discharges and to test the validity of the commonly-made assumption that they are fit well by spatially homogeneous numerical models. It turned out that the Xe^* density distribution over the discharge cross section remains homogeneous for less than 100 ns only. Comparing the experimental results of the homogeneous discharge phase with zero-dimensional model calculations, we conclude that induced emission modeled using two excited xenon levels must be taken into account for the quantitative interpretation of the absorption measurements. For the interpretation of the Xe 6s-6p absorption measurements even a multilevel model will be necessary. Further we conclude from the relative courses and the absolute values of the Xe^* particle number densities that realistic HCl kinetics should contain three vibrationally excited levels and stepwise excitation processes as proposed by Dem'yanov et al. [8].     

Tunable UV laser photolysis of organometallics with product detection by laser mass spectroscopy: Trimethylaluminum

We use tunable UV laser light in the region 200–320 nm, produced by frequency doubling the output of a dye laser, for the decomposition of organometallic compounds. This method has been applied to TMA, trimethylaluminum Al(CH₃)₃. Only the TMA monomer absorbs UV light for >220 nm. TMA decomposes by one-photon absorption mainly into two channels: aluminum atoms Al plus organic fragments, and aluminummonomethyl AlCH₃ molecules plus organic fragments. The ratio [Al]/[AlCH₃] is wavelength dependent. We present a mechanism to explain the photolysis of trimethyl compounds of group III elements (Al, Ga, In).     

Synthesen von Heterocyclen, 122. Mitt.: Über die Reaktion des Perimidons mit aktiven Malonestern

Zusammenfassung Perimidon (1) reagiert mit monosubstit. Malonsäure-trichlorphenylestern (2) bei 250° zu 9-Hydroxy-5,7-dioxo-4,5-dihydro-7H-pyrido[1,2,3-cd]perimidinen (3), die durch saure Hydrolyse zu 10-Amino-4-hydroxy-benzo[h]carbostyrilen (4) gespalten werden.

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Syntheses of heterocycles, CXXII: Reaction of perimidone with reactive malonates

Perimidone (1) reacts with monosubstituted 2.4.6-trichlorophenyl malonates at 250° to 9-hydroxy-5.7-dioxo-4.5-dihydro-7H-pyrido[1.2.3-cd]perimidines (3), which are cleaved by acid yielding 10-amino-4-hydroxy-benzo[h]quinolin-2-ones (4).

     

Positron annihilation studies in highT c superconductor YBa2Cu3Cd x O y (x=0, 0.05)

Positron lifetime and Doppler broadening of the annihilation line measurements were performed in highT _c superconducting samples YBa₂Cu₃Cd _x O _y ,x=0, 0.05 and 6.9<y<7, as a function of temperature in the region of 14–300 K. It was found that the positron lifetime and theS parameter values are lower in the Cd doped sample than those in the undoped one. It was also observed that the positron annihilation parameters show similar temperature dependence for the undoped and Cd doped samples. We conclude that the Cd doping in highT _c superconductor YBa₂Cu₃Cd _x O _y , 6.9<y<7 fills defects associated with oxygen vacancies probably in oxygen deficient regions which can trap positrons.     

Irreversible deformation of macromolecular networks

Based upon a thermodynamical approach, the generalized Onsager type of relaxation of van der Waals networks is presented. By linearly and identically coupling the set hidden variables to the network, the memory function of the system can be related to the equilibrium strain-energy function. The relaxation behavior of real networks on stretching can quantitatively be described by means of a distribution of relaxation times known from small strain experiments. Some new and interesting conclusions are discussed as to how the macroscopically non-linear visco-elastic response might be interpreted.