Direkte photometrische Bestimmung von Kobalt in Eisen, St?hlen, Erzen und Schlacken mit Nitroso-R-Salz

Zusammenfassung Die direkte Bestimmung von Kobalt in unterschiedlichen Substanzen im Gehaltsbereich von 0,001 bis 5% ist nach einem einfachen Verfahren möglich, wenn die Komplexbildungsreaktion und der tatsächliche Störeffekt durch andere Elemente bekannt sind. Die für eine Bestimmung benötigte Zeit beträgt 25 min. Die relative Standardabweichung liegt zwischen 0,02–20%.

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Direct photometric determination of cobalt in iron, steels, ores and slags using nitroso-R-salt

A simple procedure without any separation is described; the complex formation and the interfering effects of other elements are studied. This method is suitable for the accurate determination of 0.001 to 5% of cobalt in several materials. The time required for one determination is 25 min only. The coefficients of variation are within 0.02–20%.

     

pH-Dependent force spectroscopy of tri(ethylene glycol)- and methyl-terminated self-assembled monolayers adsorbed on gold

Self-assembled monolayers (SAMs) of methoxy-tri(ethylene glycol)- (EG(3)-OMe) and methyl-terminated alkanethiols (C(16)) adsorbed on polycrystalline gold were investigated by chemical force spectroscopy. Measurements were performed in aqueous electrolyte solutions depending on ionic strength and pH value. Charged and hydrophobic tips were employed as probes to mimic local patches of proteins and to study the interaction at the organic/liquid interface in detail. Force-distance curves reveal information about the origin of the observed interaction and the underlying mechanisms. The measurements confirm an effective negative surface charge to be present at the oligo(ethylene glycol) (OEG) and the methyl interface and suggest that the charges are due to the adsorption of hydroxyl ions from aqueous solution. pH-dependent measurements further support the robustness of the established charge associated with the OEG films. Its sign does not change over the whole range of investigated values between pH approximately 3.5 and approximately 10. In contrast, the hydrophobic self-assembled hexadecanethiol films on gold show an isoelectric point (IEP) around pH 4. While the mechanism of charge establishment appears to be similar for both SA films, the strength of hydrogen bonding to interfacial water, which acts as a template for hydroxyl ion adsorption, is likely to be responsible for the observed difference.     

Elevated plasma levels of haptoglobin in Duchenne muscular dystrophy:electrophoretic variants in patients with a severe form of the disease

Analysis of plasma proteins of Duchenne muscular dystrophy (DMD) patients and normal age-matched boys using two dimensional gel electrophoresis and densitometry indicated a three-fold increase in the average haptoglobin level in DMD plasma. Two electrophoretic variants of haptoglobin in which the alpha 2 chain had more basic or more acidic spots were found in DMD patients with a rapidly progressing form of the disease. The basic variant was present in relatively low amount. Possible reasons for the elevated haptoglobin levels are discussed.     

Catecholamine binding to CNS adrenergic receptors.

The properties of 3H-catecholamine binding to alpha- and beta-adrenergic receptors in CNS are reviewed. 3H-epinephrine and 3H-norepinephrine label one class of alpha-receptors throughout the brain, with high affinities for agonists and some antagonists. Agonist affinities at this site are increased in low temperature conditions but are reduced by guanine nucleotides and monovalent cations. Divalent cations reverse both effects. This alpha-receptor may be coupled to adenylate cyclase by GTP and/or sodium, and uncoupled by divalent cations. 3H-epinephrine labels beta2, but not beta1, receptors in CNS, especially in bovine cerebellum. The same beta-receptor does not show agonist-specific GTP-sensitivity, but does exhibit Na+-sensitivity. This receptor appears to be linked to adenylate cyclase, and sodium rather than GTP may be the coupling agent.     

Recherches dans la serie des metallocenes—XXVII: Stereochimies comparees de ferrocenylcyclohexenones chirales portant un carbone asymetrique quaternaire en position α ou β. Puretes optiques par dilution isotopique

The two diastereoisomeric pairs of α-phenyl α-methyl and β-phenyl β-methyl ferrocenyl cyclohexenones were prepared in optically active series from a single chiral precursor, (+) phenyl-2 methyl-2 succinic acid, the S configuration of which was established by chemical correlation. The chiral precursor and the four ketones were shown to be optically pure by isotopic dilution with tritium labelled racemates. We infer that diastereogenic cyclisation of the γ-ferrocenyl butyric acids into ketones is under pure kinetic control and leads mainly to the isomer bearing the bulkiest group in an endo position.     

A new approach to intermolecular forces in non-bonding regions

A new method to compute intermolecular energies in non-bonding regions is presented. It is based on the assumption that in such regions molecules can be reviewed as the sum of distorted, possibly overlapping, and electron exchanging atoms. The intermolecular energy change at a given distance is due to the sum of the atomic energy changes caused by these distortions. The energy change of any particular atom is computed in a Hartree—Fock model in which the effect of the other atom is represented by an effective potential. This potential in turn is computed from a calculation at a slightly larger intermolecular distance of the potential seen by an external electron in the field of the “other” atom. This potential computed in the RPA approximation and involves the distorted Hartree—Fock orbitals of the other atom (computed in a similar manner to the above) and the RPA response function of the other distorted atom.     

Projection between basis sets: A means of defining the electronic structure of functional subunits

The general problem of the transfer of the representation of a set of orthonormal functions from one basis to a different, nonequivalent one is considered and specialized to a matrix formulation convenient for use in molecular electronic structure calculations. A procedure is suggested for treating problems where the transfer of representation breaks into a subset of most interest and one of less interest as for example the occupied and virtual orbitals of a Hartree-Fock SCF calculation. These techniques are then applied to obtain a representation of a methyl group from an SCF wave function for methane.     

Zur Existenz von zwei Kristallmodifikationen der Mellitsäure

Zusammenfassung Es wurde röntgenorgraphisch und mit Hilfe derDTA, festgestellt, daß die Mellitsäure nur in einer Modifikation, der orthorhombischen¹, vorliegt. Die Darstellung der Mellitsäure^2,3 wurde in Einzelheiten modifiziert. Die Reinheit der Präparate wurde spektroskopisch, im IR- bzw. UV-Gebiet, und mit Hilfe der Papierchromatographie geprüft.

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by means of X-ray analysis and DTA it was found that mellitic acid exists only in the orthorhombic modification. The preparation of mellitic acid was modified in part. The purity ot the samples obtained was checked by IR-and UV-spectroscopy and by paper chromatography.

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Zur Kenntnis von Salzen einiger aromatischer Polycarbonsäuren, 3. Mitt.; 2. Mitt.:B. Hájek, E. Kálalová undF. Petr, Z. Chem.5, 230 (1965).

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Gewidmet dem Andenken an Professor Dr.Hans Meyer meinen Lehrer an der ehemaligen Deutschen Universität in Prag. Prof.Meyer geboren am 31. März 1871 in Wien, gestorben am 28. November 1942 in Theresienstadt, beschäftigte sich eingehend (mitH. Raudnitz u. a.) mit der Darstellung und Untersuchung der Mellitsäure und ihrer Derivate.     

Zur Automatisierung der Auswertung bei der quantitativen Spektralanalyse

Zusammenfassung Die Eigenschaften der photoelektrischen und photographischen Registrierung von Spektren werden besprochen und die Bedeutung der photographischen Registrierung für die Verfahrensentwicklung und Routineanalyse von Proben wechselnder Zusammensetzung hervorgehoben. Das Programmsystem für den elektronischen Digitalrechner und verschiedene Möglichkeiten der Datenerfassung werden beschrieben. Durch diese Automatisierung der Auswertung wird gegenüber dem herkömmlichen Rechenbrettverfahren eine Beschleunigung um den Faktor 200 erreicht.

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Summary The characteristics of the photoelectric and photographic registration of spectra are discussed and the importance of the photographic registration for the development of methods and the routine analysis of samples of changing composition is emphasized. The program system for the electronic digitalcomputer and different possibilities of data collecting are described. Automating the evaluation has resulted in a speeding-up factor of 200 compared with the traditional computing board method.

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Die obige Arbeit wurde erwähnt von Herrn Dr. Pohl am 6. 10. 1964 in Düsseldorf in seinem Vortrag Erfassen und Verwerten von chemischen Daten. [Diese Z. 209, 19 (1965).]

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Außerdem wurde uns die Arbeit von Tunnicliff und Weaver, Analytical Chemistry 36, 2318 (1964), erst nach Abschluß unserer Arbeit bekannt. Die Autoren befassen sich mit einer ähnlichen Aufgabe, wobei allerdings das Problem der Linienauswahl eingehender behandelt wird als bei uns.     

Determination of the quaternary compound ciclotropium in human biological material after hydrolysis and derivatization with the fluorophor flunoxaprofen chloride

The quantitative determination of the quaternary spasmolytic compound ciclotropium and its metabolite N-isopropyltropinium is described for human plasma and urine. The analytical procedure consists of ion-pair extraction from biological material, alkaline hydrolysis, subsequent derivatization with the fluorophor flunoxaprofen chloride and separation by high-performance liquid chromatography on a reversed-phase column with fluorimetric monitoring. The detection limits of 0.5 ng/ml in plasma and 10 ng/ml in urine at signal-to-noise ratios higher than 3 permit the determination of pharmacokinetic parameters after therapeutic doses.