Angular correlations and the tau-neutrino mass

Effects of a nonzero mass for the tau neutrinov _τ as well as a right-handed charged-current contribution to the τ?v _τ coupling are discussed. Angular correlations of the decay products of τ⁺τ^? ine ⁺ e ^? annihilation are calculated as functions of \(m_{v_\tau } \) and the relative amount of right-handed τ?v _τ coupling.     

Photochemical Rearrangement of a Steroidal α,β-Epoxylactone. Photochemical reactions,XI [1]

The UV. irradiation of 17β-acetoxy-4α, 5α-epoxy-2-oxaandrostan-3-one ( 7 ) yields 17β-acetoxy-2-oxa-10(5 → 4)abeo-4ζ (H)-androsta-3,5-dione ( 11 ). A non-photochemical synthesis of 11 , proceeding in lower yield, is also described.     

Mass spectra of some 2-methyl-3-(o- and p;-R-phenyl)-3,3a,4,5,6,7-hexahydro-2H-indazoles

The mass spectra of twelve 2-methyl-3-(o- and p-R-phenyl)-3,3a,4,5,6,7-hexahydro-2H-indazoles which have potentially useful pharmacological properties are presented.     

Organic synthesis on the microgram scale. IX

Summary Synthesis of acetanilide and analogs in good yields has been carried out ing amounts by reacting the aromatic amines with an acetic anhydride-acetic acid mixture. After TLC separation on the same vehicle, the products can be visualized by ultraviolet radiation or by color reactions. A procedure is also described to recover the acetanilides for obtaining infrared spectra by the attenuated total reflection technique.

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Zusammenfassung Die Synthese von Acetanilid und analogen Substanzen wurde mit guter Ausbeute in Mikrogrammengen durchgeführt. Man läßt das aromatische Amin mit einer Mischung von Acetanhydrid und Essigsäure reagieren. Nach DC-Trennung in diesem Laufmittel kann man die Reaktionsprodukte im UV oder durch eine Farbreaktion sichtbar machen. Außerdem wurde ein Verfahren beschrieben, die Acetanilide für die IR-Spektroskopie nach der ATR-Methode wiederzugewinnen.

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For Part VIII see Mikrochim. Acta [Wien]1971, 662.     

Organic synthesis on the microgram scale. III separation and purification of steroids

Summary This paper describes techniques for separation and purification of steroids on the thin-layer plate. Two or more operations can be performed on the same plate in order to avoid loss of material and product.When a steroid diketone (progesterone) is treated with 2,4-dinitrophenylhydrazine on silica gel, three products are obtainable. These compounds can be readily purified on the same thin-layer plate and converted to the parent steroid by means of stannous chloride in dilute hydrochloric acid.

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Zusammenfassung Trennung und Reinigung von Steroiden auf der Dünnschichtplatte werden beschrieben. Zwei oder mehr Operationen lassen sich, um Substanzverluste zu vermeiden, auf derselben Platte ausführen.Wird ein Diketosteroid (Progesteron) mit 2,4-Dinitrophenylhydrazin auf Kieselgel behandelt, so erhält man drei Reaktionsprodukte, die auf derselben Platte leicht gereinigt und mit Zinn(II)-chlorid in verd. Salzsäure in das entsprechende Ausgangssteroid zurückverwandelt werden können.

     

Tandem on-line continuous separation and determination of arsenic by inductively coupled plasma atomic emission spectrometry

The principle of tandem on-line continuous separation techniques as an alternative means of introducing samples into plasmas was applied to the development of a sensitive, selective and convenient method for the determination of arsenic by inductively coupled plasma atomic emission spectrometry (ICP-AES). Arsenic is continuously extracted as AsI₃ into xylene from the sample dissolved in 0.1 M potassium iodide solution in 7.2 M hydrochloric acid. The xylene phase (containing the analyte) is continuously mixed on-line with NaBH₄ in dimethylformamide and acetic acid solutions. Arsine is thus continuously generated directly from the organic phase and is separated in a gas—liquid separation device which prevents most of the xylene phase vapour from reaching the ICP. The system was optimized for the continuous extraction of AsI₃, the direct generation of arsine from xylene and the final ICP determination of arsenic. Finally, the tandem on-line continuous separation ICP detection system was applied to the determination of arsenic in real samples (white metal, cast iron, cupro-nickel and orchard leaves standard materials). Very good agreement between the experimental results and the certified values was obtained.     

Application of preparative high-speed counter-current chromatography for separation of methyl gallate from Acer truncatum Bunge

Preparative separation of methyl gallate in leaves extract of Acer truncatum Bunge was conducted using high-speed counter-current chromatography (HSCCC) with a solvent system composed of ethyl acetate-ethanol-water at volume ratios of 5:1:5 (v/v/v). In a single operation, 57.5 mg of methyl gallate was obtained from 120 mg of the extract. HPLC analyses of the counter-current chromatography (CCC) fraction revealed that the methyl gallate was having over 97% purity. Its structure was identified by 1H NMR and 13C NMR.     

Organic functional group analysis via gas chromatography. III

Summary A gas Chromatographic procedure for the analysis of carbamates is described. A specially prepared reaction tube, packed with a 10 % mixture of potassium hydroxide in glass beads, is placed inside the injection port of a Perkin-Elmer 900 Gas Chromatograph, in front of the Chromatographic column packed with Porapak Q. S.A solution of the carbamates (0.01–0.1mol) is injected directly into the gas Chromatograph. The carbamates are reacted with the alkali present in the reaction tube and the alcohols produced are separated, detected and recorded. Standard calibration graphs of the alcohols are prepared in the same manner and the quantities of carbamates are determined. The procedure is fast and quantitative.

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Zusammenfassung Ein gaschromatisches Verfahren für die Analyse von Carbamaten wurde beschrieben. Ein spezielles Reaktionsrohr, beschickt mit 10% iger Kalilauge auf Glasperlen, wird innerhalb der Injektionsöffnung eines Gaschromatographen Perkin-Elmer 900 vor dem mit Poropak Q. S. gefüllten Chromatographierohr angebracht. Die Carbamatlösung (0,01 bis 0,1 Mol) wird direkt injiziert. Die Carbamate reagieren mit dem im Reaktionsrohr befindlichen Alkali, die dabei entstandenen Alkohole werden getrennt, nachgewiesen und registriert. In gleicher Weise ermittelte Standard-Eichkurven der Alkohole dienen zur Bestimmung der Carbamate. Das Verfahren ist rasch und quantitativ.

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For Part II see Mikrochim. Acta [Wien]1966, 55. Inquiries and requests for reprints of this series of papers should be addressed to Prof. T. S. Ma, Department of Chemistry, City University of New York, Brooklyn, N.Y. 11210, U.S.A.     

P, p, T Surfaces of real gases and the Riemann-Hugoniot catastrophe

Analysing experimentally determined P, ?, T data of N₂, ethylene, propene, CO₂ and Xe by a new mathematical technique, we present evidence that their isothermal pressure-density dependence exhibits behaviour characteristic of a Riemann-Hugoniot catastrophe, in analogy to a van der Waals gas for above and sub critical isotherms.     

Dehydrogenation of cyclohexane over supported Pd catalysts, II. Influence of the support and reduction temperature

We have studied the activity of Pd/sepiolite and Pd/SiO₂–AlPO₄ catalysts in cyclohexane aromatization. The catalysts were characterized by H₂ chemisorption measurements. The influence of support and reduction temperature on the metal surface properties and activity of the catalysts is discussed.