Is collision-induced dissociation of low-energy carbonyl sulfide cations adversely affected by asymmetry?

We have measured relative abundances of fragment ions resulting from collision-induced dissociation of OCS(+) ions in collision with xenon neutrals as a function of ion kinetic energy and scattering angle. The lowest energy dissociation product, S(+), dominates at all energies up to 53 eV kinetic energy studied here. Surprisingly, the second most abundant dissociation channel is CS(+) and not CO(+) even though the thermochemical threshold for CO(+) is lower than that for CS(+) and CO(+) is more abundant than CS(+) in the normal mass spectrum of OCS. We do not observe any significant abundance of CO(+) in this energy range, suggesting that collision-induced excitation and dissociation of OCS(+) is significantly different to that of symmetric triatomic ions. A possible role of asymmetry in the molecular ion's collisional activation via neutral collision is suggested for the different behavior.     

Influence of the nature of organic diluents on the extraction of uranium(VI) by bis(2-ethylhexyl) sulfoxide from nitric acid solutions

The extraction of uranium(VI) from nitric acid solutions by bis(2-ethylhexyl) sulfoxide (BESO) has been examined using sixteen inert organic diluents in order to establish the correlation between its distribution coefficient and some physico-chemical properties of the diluents. The extracted solvated species is shown to be UO₂(NO₃)₂·2BESO, irrespective of their nature. The extraction rate is lower in halogen substituted hydrocarbons as compared to the other diluents used. Among benzene derivatives, extraction is found to decrease with number of substituted methyl groups. Extraction efficiency decreases as the organic solvent is varied in the order: benzene>nitromethane>toluene> >nitrobenzene>cyclohexane>p-xylene>monochlorobenzene>dodecane>o-dichlorobenzene> >hexane>decalin>1,2-dichloroethane>1,1,1-trichloroethane>carbon tetrachloride> >tetrachloroethane>chloroform. Among the properties showing good correlations with distribution coefficient are Hansen's three-dimensional solubility parameters and Dimroth's empirical solvent polarity parameters [E _T(30) ]. Polarizability indices are most satisfactorily applicable to a wide variety of solvents.     

Determination of gallium in tumour-affected tissues by means of spectroscopic techniques

A comparative investigation was carried out on the suitability of atomic absorption spectrometry and of emission spectrography with arc and hollow-cathode excitation sources for determination of gallium (μg g^-1) in biological samples. The three methods give reliable results. Hollow-cathode emission spectrography was found to be influenced to a lesser extent by matrix effects and to be more precise than the other two techniques.     

Investigation of the complex formation of plutonium(VI) with 2-thenoyltrifluoroacetone by solvent extraction

The co-ordination of plutonyl ions with 2-thenoyltrifluoroacetone (HTTA) has been investigated by distribution studies of²³⁹Pu between benzene and aqueous perchlorate medium at 25°C in order to understand the nature of the extracted species and their stability. The formation constants of the first and second complexes have been evaluated by Rydberg's graphical method as well as by least squares analysis of the distribution data using a computer programme. The overall formation constant (β₂) for Pu(VI)-HTTA system has been found to be of the order of 10¹².     

Inorganic complexes in volumetric analysis. Part III. Use of ferric fluoride complex in the estimation of iodide

Summary The method for estimation of iodide formulated in the earlier publications of the series bas been modified by the use of sodium fluoride as the complexing agent in the place of oxalate or phosphoric acid. The results obtained are in excellent agreement with the calculated ones and the method has been successfully applied for the estimation of iodide in iodized salt.     

A simple procedure for the chromatographic isolation and determination of prostaglandins from human seminal plasma

Summary A relatively simple procedure for the isolation and determination of the prostaglandins present in human seminal fluid is described. It involves preliminary chromatographic purification of these compounds from the major non-prostaglandin impurities followed by their total elution in one solvent (one-step elution). The prostaglandins thus obtained were almost free from other lipids and were further resolved into prostaglandin-groups and individual prostaglandins by repeated thin-layer chromatography. Data are also presented for prostaglandin contents of fresh semen samples from five individuals and results compared with those from the stored samples.

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Einfaches Verfahren zur chromatographischen Isolierung und Bestimmung von Prostaglandinen aus menschlichem Sperma

Zusammenfassung Das Verfahren umfaßt eine chromatographische Abtrennung der Verbindungen von den hauptsächlichsten Verunreinigungen und die Gesamtelution mit einem Lösungsmittel. Die von anderen Lipiden fast völlig freien Prostaglandine werden durch wiederholte Dünnschicht-Chromatographie in Gruppen und Einzelverbindungen getrennt. Werte werden angegeben über die Prostaglandingehalte von frischem im Vergleich zu gelagertem Sperma.

     

A measurement of the average kinetic energy released during the unimolecular decomposition of CO2 ion clusters

A combined molecular beam—mass spectrometer apparatus has been used to measure the average kinetic energy E_t released during the unimolecular decomposition of CO₂ ion clusters in the field-free region of the mass spectrometer. For the reaction (CO₂), _n→ (CO_2n?1+CO₂, the measured value for E_t is found to increase as n increases from 3 to 13.     

Stability constants of some bivalent metal complexes of N-phenyl-o-tolylbenzohydroxamic acid

The stability constants of the Cu²⁺, Zn²⁺, Ni²⁺ and Mu²⁺ complexes of N-phenyl-o-methoxybenzohydroxamic acid at 30° in 50% v/v aqueous dioxan are: log K₁ 10·45, 8·16, 7·52, 6·33; log K₂ 8·90, 6·70, 6·01, 5·59 (for the ions in the order given).