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  • Analytical Chemistry and Spectroscopy  (59)
  • Inorganic Chemistry
  • Superfluidity and superconductivity
  • 2015-2019
  • 1975-1979  (85)
  • 1950-1954
  • 1930-1934
  • 1925-1929
  • 1975  (85)
Collection
Publisher
Years
  • 2015-2019
  • 1975-1979  (85)
  • 1950-1954
  • 1930-1934
  • 1925-1929
Year
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 304-306 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The identification of 6-methoxy 8-aminoquinoline as a metabolite of Primaquine, an important antimalarial drug, is described. The metabolite is present in urine, plasma and erythrocytes following drug ingestion. It was identified by mass fragmentography of its 1H and 2H acetate and the acetate produced from authentic material. No evidence of further metabolites was obtained.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 10 (1975), S. 1102-1110 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of a variety of authentic carotenoids covering a range of structural types have been studied using the field desorption technique. All the compounds examined show the molecular ion as the base peak, even where this ion is of very low intensity in the electron-impact spectra. Little fragmentation is observed, but thermal decomposition can be induced in certain cases by using higher emitter currents. Application to a simple mixture of authentic compounds and a more complex mixture of sedimentary origin shows the potential of the method in the rapid qualitative screening of carotenoids in crude extracts.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 7 (1975), S. 154-159 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H NMR spectra are reported for Michler's ketone and twenty of its derivatives, along with 13C chemical shifts for five of the compounds. 1H chemical shifts show only small changes with increasing substitution at the sterically hindered 2-position. Estimates of the dihedral angle between the benzene ring and C—CO—C planes have been obtained from the chemical shifts of C=O and 4-C for ketones 1, 3, 5, 15 and 16. These angles are both internally consistent and very similar to dihedral angles determined by other methods for corresponding compounds in the benzophenone series.
    Additional Material: 1 Ill.
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  • 4
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Computer fitting techniques have been used to derive a new expression for the relationship between X-ray continuum intensity and atomic number for a range of electron acelerating potentials up to 25 kV, continuum energies up to 10 keV and average atomic numbers up to thirty. A practical approach to background corrections in energy dispersive electron microprobe analysis, which utilizes this expression, is outlined. The procedure should lead to significant improvements in both accuracy and detection limits in this method of X-ray analysis.
    Additional Material: 6 Ill.
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  • 5
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 29Si-NMR Spectroscopy of Silicate Solutions. II. On the Dependence of the Structure of Silicate Anions in Water Solutions from the Na : Si RatioThe 29Si-FT-NMR spectra of 13 sodiumsilicate solutions with different Na:Si ratios are investigated with regard to the structure of the silicate anions in the solutions. The 5 typical building units (Monosilicate, end-, middle-, branching and crosslinking groups) show characteristic and non overlapping ranges of the 29Si chemical shift with many signals splittings caused by different neighbouring group effects. The relative intensities of the signals give informations on the concentrations and the equilibrium of condensation of the silicate anions in dependence of the Na:Si ratio. It is shown, that many types of anions with different degree of condensation coexist in an equilibrium, which is shiftet to the polymer silicate anions with high content of branching and crosslinking groups on the decrease of the Na:Si ratio.
    Notes: Die 29Si-FT-NMR-Spektren von 13 Natriumsilicatlösungen mit unterschiedlichem Na:Si-Verhältnis werden in Hinblick auf die Struktur der in den Lösungen auftretenden Silicatanionen untersucht. Für die 5 möglichen Baugruppen (Monosilicat, Endgruppen. Mittelgruppen, Verzweigungs- und Vernetzungsgruppen) lassen sich definierte Bereiche der 29Si-chemischen Verschiebung angeben, in denen durch Einfluß der weiteren strukturellen Umgebung i. a. zahlreiche Signalaufspaltungen beobachtet werden. Aus den relativen Intensitäten der Signale können Aussagen über die Konzentrationsverteilung und damit über das Kondensationsgleichgewicht der Silicatanionen in Abhängigkeit vom Na:Si-Verhältnis abgeleitet werden. Es zeigt sich, daß zahlreiche Anionentypen mit unterschiedlichem Kondensationsgrad nebeneinander in einem Gleichgewicht vorliegen, das sich mit fallendem Na:Si-Verhältnis stark auf die Seite höhermolekularer Silicatanionen mit hohem Gehalt an Verzweigungs- und Vernetzungsgruppen verschiebt.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1655-1658 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,2,3-Butatrien durch Diels-Alder RetrogressionThe pyrolysis of 1 leads to indane (6), whereas 2,3, and 4 yield 1,2,3-butatriene (5) by a Diels-Alder-retrogression.
    Notes: Die Pyrolyse von 1 führt zu Indan (6), während 2,3 und 4 unter Diels-Alder-Spaltung zerfallen und 1,2,3-Butatrien (5) liefern.
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  • 7
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Acetylenes with Transition Metals, IV. Structure of the Complex Obtained from 2,5,5-Trimethy-3-hexin-2-ol and Bis(benzonitril)palladium ChlorideBy reaction of 1 with (C6H5CN)2-PdCl2 results the complex 15 which furthermore changes in the stable complex 3. The structures 3 and 15 were supported by chemical behaviour and spectroscopic data.
    Notes: Bei der Umsetzung von 1 mit Bis(benzonitril)palladiumchlorid wird als erstes Reaktionsprodukt der Komplex 15 isoliert, der sich weiter in den Komplex 3 umwandelt. Die Strukturen 3 und 15 werden chemisch und spektroskopisch untermauert.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 23-30 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An ion doublet chemical ionization mass spectrometry technique was utilized for the rapid detection and elucidation of the structure of a new hydroxylated metabolite of the oral anticoagulant warfarin. This technique involves the use of a 50:50 mixture of stable isotope labeled and unlabeled drug. With this procedure ions found in the mass spectrum which are associated with the administered drug can be identified unambiguously. The unknown metabolite from rat liver microsomal preparations was identified as benzylic hydroxywarfarin by reincubating the microsomes with warfarin specifically labeled in the benzylic position and observing the subsequent loss of label in the product. The ion doublet technique was also employed in a single human study, and benzylic hydroxywarfarin was detected and identified.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 126-130 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method is described for the micro-identification of both mono- and diesters of 12-deoxyphorbol based upon a combination of thin-layer chromatography and mass spectrometry. The technique may be used on as little as 5 ml of fresh plant latex. Nine thin-layer systems are described, six of which are adsorption systems based on silica gel or alumina as adsorbent, and three are partition systems using diethyleneglycol as stationary phase. The migration by means of thin-layer chromatography is dependent upon the chain length of the C-13 esterifying acid and on the presence or absence of a free primary hydroxyl group at C-20. By means of mass spectrometry it was possible to confirm the identity of the esterifying moiety at both the C-13 and C-20 positions of 12-deoxy-4βOH-phorbol.
    Additional Material: 4 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 2 (1975), S. 201-203 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High resolution photoplate mass spectrometry has been used to examine crude goat urine extracts to determine the fate of organochlorine xenobiotics in these animals. Using a direct introduction temperature controlled probe the crude urine extracts were analyzed and the presence of oxygenated metabolites of 4-chlorobiphenyl and 4,4′-dichlorobiphenyl were confirmed in goats; analyses of urine extracts from goats injected with the commercial Aroclor mixtures 1254 and 5460 confirmed the formation of oxygenated penta-, tetra- and monochlorobiphenyl metabolites and an oxygenated dichloroterphenyl metabolite, respectively. This technique was particularly useful in the analysis of complex mixtures of metabolites.
    Additional Material: 1 Ill.
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