Ultra-violet excited laser emission in Na2

Laser emission at different wavelengths in the range of 903–914 nm and around 2.5 m has been observed upon excitation of Na₂ by uv radiation from an excimer laser at 351 nm and an excimer pumped dye laser in this wavelength range. The emission is attributed to a cascade emission followed by . In addition, coupled with the laser emission around 910 nm, broad-band fluorescence peaking around 855.5 nm is observed which, eventually, may be the first observation of the bound-free transition in Na₂.     

Limit on right handed weak coupling parameters from inelastic neutrino interactions

Right handed weak quark currents coupled to the usual left handed weak lepton current would be seen in inclusive antineutrino scattering on nuclei as a contribution at largey with the quark (not antiquark) structure function. We do not see such a term, and can therefore put an upper limit on the relative strengths of such right handed currents: \(\varrho ^2 = \frac{{\sigma _R }}{{\sigma _L }}< 0.009\) , 90% confidence. This measurement puts limits on the mixing angle of left-right symmetric models. In distinction to similar limits derived from muon decay or β decay, our limits are also valid if the right handed neutrino is heavy.     

Synthesis and investigation of mono- and binuclear cyano-bridged complexes of rhodium,ruthenium, and palladium

Binuclear Rh^III and Ru^II complexes of the [M¹-CN-M²]⁺BF ₄ ^– (M¹ and/or M² are (⁵-Cp)(³-C₃H₅)Rh and (⁶-C₆H₆)(³-C₃H₅)Ru) type, heteronuclear organometallic compound (⁵-Cp)(³-C₃H₅)RhCNPd(³-C₃H₅)Cl, and mononuclear Rh^III and Ru^II complexes [(³-C₃H₅)LM(MeCN)]⁺ _BF4 ^– (M = Rh, L = ⁵-Cp; M = Ru, L = ⁶-C₆H₆) were synthesized. An electrochemical study of these compounds in solutions demonstrates that the bond between the bridged CN ligand and the metal atoms is rather strong, and there is no dissociation into mononuclear fragments in solutions. The kinetics of the reaction of [(⁵-Cp)(³-C₃H₅)Rh(MeCN)]⁺ _BF4 ^– with halide ions was studied by electrochemical methods. The ligand exchange proceeds by a bimolecular dissociative-exchange mechanism.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 968–973, May, 1995.     

13C NMR Spectra of polycyclic compounds: stereochemistry of spiro(bicyclo[2.2.1]hepta-2,5-diene-7,1′-cyclopropane) dimers

The structures of the dimerization products of spiro(bicyclo[2.2.1]hepta-2,5-diene-7,1-cyclopropane) have been solved using¹³C NMR spectroscopy and their stereochemical assignments made. The methylene carbon atom signals for the spirocyclopropane fragment can be used as diagnostic signals in making the stereochemical assignments.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 559–564, March, 1990.     

Thermodynamic study of complex formation between 18-crown-6 and potassium ion in some binary non-aqueous solvents using a conductometric method

The complexation reaction between a macrocyclic polyether, 18-crown-6 (18C6), and potassium ion was studied in methanol (MeOH)-acetonitrile (AN), dimethylformamide (DMF)-AN and propylecarbonate (PC)-DMF binary solvent systems at different temperatures using a conductometric method. It was found that the stability of the 1:1 complex formed between K(+) ion and this ligand increases with decreasing temperature. Standard enthalpies and standard entropies of the complex formation were obtained from the temperature dependence of the stability constant. In all cases negative DeltaH(o)(c) and DeltaS(o)(c) values characterize the formation of 18C6-K(+) complex. The results obtained show that the stability of the complex is governed by the solvent medium and the thermodynamic parameters DeltaH(o)(c), DeltaS(o)(c) and DeltaG(o)(c) are sensitive to the composition of the mixed solvents. In addition, it was found that the stability constant of the resulting 1:1 complex among various neat solvents used varies in the order PC > MeOH > AN > DMF.     

Effect of epitaxial growth on the formation of the cobalt catalysts of the Fischer-Tropsch synthesis

Mixed oxides Co_xAl_yO₄ with different Al/Co ratios applied as supports for the catalysts of the Fischer-Tropsch synthesis were prepared using the solid-state chemical reaction. The Co_xAl_yO₄ supports were prepared by modifying gibbsite with various cobalt salts (acetate, nitrate, and basic carbonate). The use of basic cobalt carbonate gives the Co(20%)/Co_xAl_yO₄ catalyst, which provides an increased yield of hydrocarbons C₅₊ and a decreased methane content compared to the impregnation catalyst Co(30%)/Al₂O₃. The introduction of small amounts of rhenium additives makes it possible to enhance the yield of hydrocarbons C₅₊ (179 g m⁻³) and also to increase the selectivity with respect to the C₅–C₁₈ fraction. The introduction of basic cobalt carbonate into the support, most likely, creates favorable conditions for the epitaxial growth of the precursor of the active phase. Dedicated to Academician G. A. Abakumov on the occasion of his 70th birthday. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1856–1860, September, 2007.     

The effect of the relative location of the double bond and the alkoxy group on the mass-spectrometric behavior of alkoxydihydropyranes

Conclusions The mass spectra ofthree 6-alkoxy-³-dihydropyranes and of three 6-alkoxy-²-dihydropyranes have been studied. As distinct from the previously studied 2-alkoxy-³-dihydropyranes, the dominant fragmentation pattern for the compounds under investigation is by retrodiene degradation. Furthermore, in the case of the ²-isomers the charge is preferentially localized on the olefin fragment while for the ³-isomers, it is located on the diene fragment.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1442–1444, June, 1970.     

The synthesis of N-substituted 5-aminofurfurals

A simple method for the synthesis of N-substituted 5-aminofurfurals based on the reaction of 5-halogenofurfurals with secondary amines has been developed. The reaction takes place through the formation of quaternary salts of N-substituted 5-aminofurfurals. 5-(Diethylamino)-, 5-(N-methyl-N-phenylamino)-, and 5-piperidinofurfurals have been obtained for the first time.     

Introduction of the aminooxy group on to nitroaromatic and heterocyclic rings : Synthesis and properties of O-(nitroaryl)hydroxylamines

The reaction of halonitrobenzenes with t-butyl N-hydroxycarbamate (2), gave t-butyl N(nitroaryloxy)carbamates (3), which yielded on acidolysis with trifluoroacetic acid, O-(nitroaryl)hydroxylamines (4). Compounds 4 were utilized for the amination of anionic nitrogens and of carbanions. Attempts to apply the method to the synthesis of hydroxylamines substituted on the oxygen by heterocyclic rings (pyridine, pyrimidine, pyrazine, triazine, purine and benzothiazole) yielded only the corresponding hydroxy compounds. However, the formation of a N,O-dipyridylhydroxylamine derivative (22b) indicates that O(5-nitro-2-pyridyl)hydroxylamine (17) existed as a highly reactive intermediate.