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  • Chemistry  (169)
  • Atomic, Molecular and Optical Physics  (1)
  • 42.75
  • Wiley-Blackwell  (170)
  • 1975-1979  (46)
  • 1960-1964  (124)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 1735-1745 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Infrared spectroscopy was used for the determination of the base-pairing content of four specific tRNAs in deuterium oxide solution. Infrared spectra were obtained in the 1750-1550 cm-1 region at various temperatures ranging from about 15 to 90°C. Melting curves were constructed by plotting the molar extinction coefficient at ν = 1657 cm-1 versus temperature. These transition curves enabled us to determine the ranges of temperature which correspond to the ordered (partially double-stranded) or randomly coiled structure of the tRNA. For a set of wavenumbers the extinction coefficients at these temperatures were used for the calculation of the base-pairing content. The procedure employed here is based on a method described earlier by Thomas [(1969) Biopolymers 7, 325-334]. For the conditions selected for this investigation (Mg2+-free D2O-buffer; 0.01M tris-DCl, 0.015M NaCl, pD 7.5) the results of this determination agree within the limits of errors with the number of base pairs predicted by the cloverleaf model.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 1296-1304 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Darstellung der freien Farbsäuren des Betanins und Betanidins wird beschrieben, ihre Bruttoformeln werden erörtert. Beide Verbindungen sind optisch aktiv. Sie spalten mit starker Natronlauge in der Hitze etwa 1/3 ihres Stickstoffes als Ammoniak ab. Quantitative Decarboxylierungsversuche und potentiometrische Titration weisen für das Glucosid wie für das Aglykon auf drei Carboxylgruppen, von denen eine durch eine basische Gruppe neutralisiert zu sein scheint, und eine schwach saure (phenolische) Gruppe hin. Beim oxydativen Abbau des Betanidins wurde L-Asparaginsäure erhalten.
    Additional Material: 2 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 2761-2776 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dehydro-digallussäure (I) und Valoneasäure-dilacton (II) erleiden mit Alkalien eine Spaltung an der Diphenyläther-Brücke, die keine Hydrolyse ist. Anhand zahlreicher Modellsubstanzen wird festgestellt, daß diese neuartige Spaltung von Diphenyläthern offenbar an das Vorliegen von 3 vicinalen, freien Hydroxygruppen an einem der beiden Phenylreste gebunden ist. Die Spaltung ist eine innere Disproportionierung; als Mechanismus wird eine β-(oder vinyloge β-)Eliminierung diskutiert. - Sieben einseitig hydroxyl-substituierte Diphenyläther wurden neu dargestellt.
    Additional Material: 3 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 93 (1960), S. 556-557 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 12 (1977), S. 805-811 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The PCILO method was used to study systems with the following types of intermolecular hydrogen bonds, involving 2nd row atoms: N…H—S, S…H—S, N…H—Cl, Cl…H—F, Cl…H—Cl, P…H—N, P…H—P, P…H—F, S…H—F.In all the cases calculated, the PCILO method yields an accurate qualitative description of the stabilization energies and to some extent quantitatively good agreement with reliable ab initio and experimental results. The corresponding equilibrium distances are in almost all cases smaller (up to 0.6 Å) than the ab initio values of the same compounds.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Organic radicals were produced in the tensides C16H33(OCH2CH2)21OH and C14H29(OCH2CH2)3-SO3Na in aqueous solutions using a short pulse of high energy electrons. The radicals were formed by OH attack on the (OCH2CH2)x-parts of the tensides. The decay of the 250nm absorption of the radicals was recorded at different initial radical concentrations and tenside concentrations. Several radicals could be produced in one micelle. Radicals formed in the same micelle decay within microseconds or faster. The half life time τ1 in a micelle carrying two radicals is 2,0·10-6 s for C16H33(OCH2CH2)21 OH and less than 6·10-7 s for C14H29(OCH2CH2)3SO3Na. A model for intramicellar radical-radical reactions is proposed according to which the rate is faster in tensides of high critical micelle concentration. Single radicals in micelles of C16H33(OCH2CH2)21OH can deactivate each other without leaving the micelles. This intermicellar reaction is discussed in terms of the rate of diffusion-controlled micelle-micelle encounters, an encounter time of 7·10-8s, and the above time τ1 for intramicellar reaction. The observed rate constant 2k of intermicellar reaction is 3,5·106 mol-1·l·s-1. At low tenside concentrations, the bimolecular rate constant increases since more single tenside radicals are present in solution. They react rapidly (ca. 108 mol-1·l·s-1) with radicals in micelles. Single radicals in C14H33(OCH2CH2)3-SO3Na micelles cannot directly react with each other because of the Coulombic repulsion between two anionic micelles. Reaction occurs after the exit of a tenside radical from its micelle, the rate of which depends on the micellar equilibrium Mn⇄Mn-1+M (M: tenside molecule; n: agglomeration number of micelle). A single radical in solution reacts with a single radical in a micelle with 2k = 1,0·108 mol-1·l·s-1 and with another single radical in solution with 4,0·107 mol-1·l·s-1.γ-Irradiation of both tensides in aqueous solution leads to slight increases in viscosity, followed by turbidity beyond the “gel dose” and phase separation. These effects are explained in terms of crosslinking of tenside molecules. Formation of a large network requires bridges between all participating tenside molecules (not only bridges between micelles).
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 1 (1978), S. 97-97 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography ; Structure and relation of polyhalogenated aromatics ; discussed ; Silica gel/aluminium oxide compared ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Separation of polychloro biphenyls ; Separation of organochlorine pesticides ; Splitless automated injection ; Residue level ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complicated PCB mixtures can be separated in individual compounds using glass capillary gas chromatography, (GC)2. Depending on extraction and clean-up procedure it is also possible to separate and determine organochlorine pesticides at the same time.This (GC)2 technique can be used to determine the contents of individual chlorinated biphenyls in milk products and animal feedstuffs and in the analysis of complicated extracts of soil and vegetable material.Practical aspects concerning connection of the capillary, automatic splitless injection, repeatability of the retention time, quality of the column with respect to separation and adsorption and degradation of DDT are discussed.The detection of individual chlorinated biphenyls is possible at the ppb level in fats and vegetable materials, using an extraction and clean-up procedure, based on saponification of the sample.Preliminary results for milk, obtained from several areas, are shown.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 12 (1961), S. 560-569 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Observations concerning primary and secondary passivationPotentiostatic and galvanostatic measurements in sulphuric acid electrolytes have been carried out on high-purity ironchrome alloys with chromium contents ranging from 5 to 70 per cent., as well as on high-purity chromium. These measurements were supplemented by the examination of passivation curves, using the galvanostatic insertion method.The passivation currents thus measured were found to differ considerably from the values known so far. The newly found values can be calculated with the aid of an approximation formula as a function of the chromium content. Apart from the “primary” passivation, it was possible, in the concentration range from about 10 to about 40 per cent. Cr, also to observe the „secondary“ passivation which is likewise governed by the current (i) / time (t) law characteristic for passivation generally: (i - i0) t = const. As this phenomenon is greatly dependent on the pH value of the electrolyte and on the presence of complex-forming substances, it is suggested that the phenomenon might be explained by the formation, due to hydrolysis of a second passivation layer.It is assumed that, in the state of “primary passivation” the alloys are covered by a very thin film comparable to that of passive chromium, and that this film is then covered by a “secondary” passivation layer of greater thickness, similar to the iron passivation layer.In the zone of primary passivation, the alloys are anodically dissolved over the whole area whilst, the zone of secondary passivation, strong pit corrosion can be observed.
    Notes: Es wurden an sehr reinen Eisen-Chrom-Legierungen mit Cr-Gehalten von 5 bis 70% sowie an reinstem Chrom potentionstatische und galvanostatische Messungen in Schwefelsäureelektrolyten durch geführt, die durch die Untersuchung von Passivierungskurven nach der galvanostatischen Einschaltmethode ergänzt wurden.Für die Passivierungsstrommengen wurden Werte gefunden, die von den bisher bekannten erheblich abweichen. Die neu ermittelten Werte lassen sich in Abhängigkeit von Cr-Gehalt der Legierungen durch eine Näherungsformel berechnen. Neben der „primären“ konnte im Konzentrationsbereich von etwa 10 bis 40% Cr auch die „sekundäre“ Passivierung beobachtet werden, für die ebenfalls das die Passivierung kennzeichnende Strom(i)-Zeit(t)-Gesetz (i-i0) = const. gilt. Wegen der starken Abhängigkeit dieses Vorganges von pH-Wert des Elektrolyten und der Anwesenheit von Komplexbildnern wird zu dessen Erklärung die hyrolysebedingte Bildung einer zweiten Passivschicht vor geschlagen.Es wird angenommen, daß die Legierungen im „primärpassiven“ Zustand mit einer sehr dünnen Schicht belegt sind, die mit derjenigen des passiven Chroms vergleichbar ist und auf der sich bei der „sekundären“ Passivierung eine dickere zweite Schicht aufbaut die einer Eisenpassivschicht ähnelt.Im primärpassiven Gebiet werden die Legierungen auf der ganzen Fläche anodisch aufgelöst, während im sekundärpassiven Bereich starke Lochfraßbildung beobachtet wird.
    Additional Material: 21 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 9 (1978), S. 406-413 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Form and Mechanisms of Cracks and Fractures Caused by Simultaneous Corrosive and Dynamic Stress under Various FrequenciesDistinction of crack nucleation and crack propagation under variable frequencies and electrolytic corrosion. Relationship between crack nucleation and frequency due to differing sliding mechanisms. Crack propagation under decreasing frequencies causes transition from corrosion fatigue to cyclic stress corrosion cracking and finally stress corrosion cracking can be observed. Coordination of that transition with the increasing influence of the KISCC-value as determinant of the crack propagation.The influence of frequency on high temperature materals in hot gas atmosphere is mainly determined by creep mechanisms during top-load phase and the gas-metal-reactions. Accordingly the life time increases with growing load frequency.
    Notes: Anrißphase und Phase des Rißfortschritts bei der Betrachtung der Frequenzabhängigkeit unter elektrolytischer Korrosion. Abhängigkeit der Anrißphase von der Frequenz infolge unterschiedlicher Gleitmechanismen. Beim Rißfortschritt erfolgt mit sinkender Frequenz Übergang von Schwingungsrißkorrosion zu zyklischer Spannungsrißkorrosion und schließlich zu Spannungsrißkorrosion. Zuordnung dieses Übergangs zum zunehmenden Einfluß des KISCC-Wertes als Bestimmungsgröße für den Bruchvorgang.Frequenzabhängigkeit bei Hochtemperaturwerkstoffen in Heißgasatmosphäre im wesentlichen bestimmt durch Kriechvorgänge bei Einwirkung der Oberlast und zeitabhängige Gas-Metall-Reaktionen. Entsprechend verlängern sich die Standzeiten mit zunehmender Belastungsfrequenz.
    Additional Material: 16 Ill.
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