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141.
An experimental investigation on the possibility of obtaining tunable, multiple wavelength output in mixture of dyes pumped by a nitrogen laser has been carried out. A great number of binary dye mixtures have been tested. Simultaneous two wavelength operation is generally possible provided the gain profiles of both dyes are neither strongly overlapped nor too widely separated. Three color emission is feasible in many mixtures, but the possible combinations are limited. A simple scheme for multiple, simultaneous wavelength tuning is presented.  相似文献   
142.
Two hundred ninety experimental absolute intensities of nu(1) and nu(3) transitions of ozone have been measured, with good accuracy (<2%). They are used to derive the transition-moment parameters for these bands. The agreement between our observed and calculated line intensities is satisfactory. This work shows that the intensities of these two bands are on average 4% smaller than those used in the literature. In addition, 20 intensities of the nu(2) + nu(3) - nu(2) band confirm this value. Also, 42 line intensities of the 2nu(1)-nu(3) band are reported. Copyright 2001 Academic Press.  相似文献   
143.
144.
Raman and resonance-Raman spectra of the I?3 ion isolated within CsI crystals have been studied using 647 nm and 488 nm exciting radiation. Sample temperatures between 300 and 20 K have been used. Eleven overtones of the symmetric stretching mode (nν1) have been observed in the resonance-Raman spectrum excited by the 488 nm Ar+ laser line. Bands centred at 153, 170, 264 and 304 cm?1 have been assigned as ν3, 2ν2, ν13 and 2ν3+) respectively. The remaining structure between the nν1 lines has been assigned as due to combinations of these lines with the lattice vibrations of the CsI crystal.  相似文献   
145.
Aromatic ketones are enantioseletively hydrogenated in alcohols containing [RuX{(S,S)‐Tsdpen}(η6p‐cymene)] (Tsdpen=TsNCH(C6H5)CH(C6H5)NH2; X=TfO, Cl) as precatalysts. The corresponding Ru hydride (X=H) acts as a reducing species. The solution structures and complete spectral assignment of these complexes have been determined using 2D NMR (1H‐1H DQF‐COSY, 1H‐13C HMQC, 1H‐15N HSQC, and 1H‐19F HOESY). Depending on the nature of the solvents and conditions, the precatalysts exist as a covalently bound complex, tight ion pair of [Ru+(Tsdpen)(cymene)] and X?, solvent‐separated ion pair, or discrete free ions. Solvent effects on the NH2 chemical shifts of the Ru complexes and the hydrodynamic radius and volume of the Ru+ and TfO? ions elucidate the process of precatalyst activation for hydrogenation. Most notably, the Ru triflate possessing a high ionizability, substantiated by cyclic voltammetry, exists in alcoholic solvents largely as a solvent‐separated ion pair and/or free ions. Accordingly, its diffusion‐derived data in CD3OD reflect the independent motion of [Ru+(Tsdpen)(cymene)] and TfO?. In CDCl3, the complex largely retains the covalent structure showing similar diffusion data for the cation and anion. The Ru triflate and chloride show similar but distinct solution behavior in various solvents. Conductivity measurements and catalytic behavior demonstrate that both complexes ionize in CH3OH to generate a common [Ru+(Tsdpen)(cymene)] and X?, although the extent is significantly greater for X=TfO?. The activation of [RuX(Tsdpen)(cymene)] during catalytic hydrogenation in alcoholic solvent occurs by simple ionization to generate [Ru+(Tsdpen)(cymene)]. The catalytic activity is thus significantly influenced by the reaction conditions.  相似文献   
146.
Marked increases in the concentrations of thorium and uranium isotopes observed in rain samples collected at Fayetteville (36° N, 94° W), Arkansas, during 1983 are attributed to the fallout from the 1982 eruption of El chichón volcano in Mexico.This investigation was supported by the National Science Foundation under Grant ATM 82-06718 and ATM 84-07618.  相似文献   
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