56,57,60CoFe NMR/ON,hyperfine anomalies and γ-factors of cobalt isotopes

The results of NMR/ON measurements on^56'57'60Co isotopes in iron are presented. To avoid the uncertainties caused by local demagnetizing field inhomogenities the measurements on two cobalt isotopes in one sample have been carried out. The values of nuclear-factor ratios ⁵⁷/ ⁶⁰ = 1.805 (20), ⁶⁰/ ⁵⁶ = 0.761 (20), ⁵⁶/ ⁵⁷ = 0.726 (20) and hyperfine anomalies⁵⁶⁶⁰ = -0.036 (10),^{60 57} = 0.017 (10) and⁵⁷⁵⁶ = 0.018 (10) have been calculated from the experimental results.     

Birefringence in YAlO3∶Ce between 2–5 eV

This contribution presents birefringence spectra for orthorhombic YAlO₃Ce single crystal in the region 2–5 eV. The spectra were measured by means of a reflection method of null ellipsometry and were compared with spectra of YAlO₃:Nd determined from values measured in the region of lower energies (1·1–2·2 eV). We have found that there are differences between the spectra of YAlO₃Nd and YAlO₃:Ce which are most pronounced in thea-axis direction.The author is most grateful to Ing. . Viovský CSc. for helpful discussions during the course of this work and to Monokrystaly Turnov for preparation of the samples.     

Hyperfine anomalies and nuclear γ-factors of56Co,57Co and60Co isotopes studied by NMR/ON

The results of NMR/ON measurements on^56,57,60Co isotopes in iron are presented in the paper. To avoid the uncertainties caused by local demagnetizing field inhomogeneities the measurements on two cobalt isotopes in one sample have been carried out. The values of nuclear-factors ratios ⁵⁷/ ⁶⁰=1·805(20), ⁶⁰/ ⁵⁶ = 0·761(20), ⁵⁶/ ⁵⁷ = 0·726(20) and hyperfme anomalies^{56 60} = –0·036(10),^{60 57} = 0·017(10) and^{57 56} = 0·018(10) have been calculated from the experimental results.Dedicated to the 30th anniversary of the Joint Institute for Nuclear Research.     

Cinnamaldehyde hydrogenation using ruthenium-tin catalyst type

Bimetallic ruthenium-tin catalysts were prepared using the sol-gel method and the method of carrier impregnation. Two different procedures were used for their reduction — reduction in hydrogen atmosphere under an increased temperature, and reduction using an aqueous solution of sodium borohydride. Hydrogenation of 3-phenylpropenal (cinnamaldehyde) in tetrahydrofuran at 433 K and the total pressure 7 MPa was used as the model reaction for comparing the catalytic properties of the prepared catalysts. It was demonstrated that a tin addition notably affected catalytic properties of ruthenium in the sense of a selectivity increment related to the production of an unsaturated alcohol.     

Photocatalytic TiO2 Coatings: Effect of Substrate and Template

Summary. Transparent TiO₂ films with a high photodegradation activity towards an azo dye in aqueous solution were prepared by sol–gel processing. Films on soda–lime glass supports protected with a thin silica barrier layer exhibited better crystallization and monodisperse nanoparticles, higher absorption of light below 370 nm, and higher photocatalytic activity than those films deposited on bare glass supports proving the detrimental effect of interdiffused sodium ions on the development of the anatase nanostructure. The effect of substrate was more pronounced in thinner films (300 nm) than in thicker ones (1200 nm), which were achieved by adding a template (i.e. Pluronic F127) to the sol.     

Formale Redoxpotentiale einiger Aminophenoxazone

Zusammenfassung Mit Hilfe von Gemischen wurden die formalen Redoxpotentials einiger einfacher Aminophenoxazone-(3) und 2-substituierter Gallocyaninmethylesterderivate (Prune) mit den Substituenten — NH-C₆H₄X [X = H, CH₃, OCH₃, OH, NH₂, N(C₂H₅)₂] in 50%iger Äthanollösung mit einer konstanten Ionenstärke in der Abhängigkeit vom pu bei 25° C gemessen.Die auf p_H=0 extrapolierten Potentiale stehen mit den Hammetschen -Konstanten in guter Korrelation.

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Summary With the aid of mixtures the formal redox potentials of several simple aminophenoxazones-(3) and 2-substituted gallocyaninmethylester derivates (Prunes) with the substituents -NH-C₆H₄X [X = H, CH₃, OCH₃, OH, NH₂, N(C₂H₅)₂] were measured in 50% ethanol solution with a constant ionic strength with respect to the dependence of pn at 25° C. The potentials extrapolated to pn = 0 are in good correlation with the Hammet -constants.

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Wir danken Herrn Ing.Z. Stránský C. Sc. für wertvolle Erinnerungen bei der Interpretation der Ergebnisse.     

Synthesis of new 3-(phenoxyphenyl)sydnones marija Šindler-kulyk

The title compounds were prepared by dehydrocyclization of corresponding substituted N-nitrosoglycines obtained from isomeric o-, m- and p-aminodiphenyl ether with ethyl bromoacetate and subsequent nitrosation of the intermediate N-arylsubstituted glycines.     

Cyclic chronopotentiometry of nickel(II) at mercury electrodes in acidic perchlorate solutions: Case of higher order nonregenerative reactions following electron transfer

The reduction of Ni²⁺ ions at mercury electrodes in acidic perchlorate solutions, at perchlorate concentrations below 0.2 M, is characterized by absence of kinetic control in the preceding step, and by a complex reaction mechanism following the electron transfer. This reaction sequence is known to involve intermetallic compound formation between Ni and Hg and is best described, as shown here, by a parallel second and third order kinetic scheme. Apparent rate coefficients for this kinetic scheme were determined using cyclic chronopotentiometric data and fitting by digital simulation. A linearization test of computed kinetic rate coefficients versus the number of transitions permits quantitative tests of validity of assumptions made.     

Electronic structure and spectra of tetrathiotetracene and related molecules

The electronic spectra of tetrathiotetracene (TTT) and of its mono- and dipositive ions have been calculated by the Pariser-Parr-Pople (PPP) method. Furthermore, the band polarizations of the first two bands of TTT have been measured. A reasonable band assignment is given using a new set of PPP parameters based on spectral data of a naphthalene derivative containing similar typical weak S-S bond. Other physical parameters as ionization potential, disproportionation energy, S-S bond length and net π-charges are discussed.