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  • Inorganic Chemistry  (1,485)
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  • 2015-2019
  • 1975-1979  (3,469)
  • 1979  (1,788)
  • 1978  (1,681)
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  • 2015-2019
  • 1975-1979  (3,469)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 25 (1979), S. 763-773 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A theoretical and experimental analysis of self-inducting turbo aerator performance was carried out based on the theory of water jet injector operation. It was shown that the aerator's injection coefficient is completely determined by only two dimensionless groups, CH and EuG, between which there is a single valued dependence on whose basis generalization of experimental data is possible. An analytical expression for the optimality criterion or aerator performance index, accounting for aerator gas capacity, power consumption, and submergence, has been obtained in terms of CH and EuG with only one adjustable parameter. From the above two dependencies, a methodology was developed for determining optimal operating conditions, by means of which all the data necessary for the optimal design can be obtained from the results of bench scale experiment.
    Additional Material: 12 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 101 (1979), S. 57-65 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The concentration of trace elements in L-cells has been studied as a function of the trace metal content of the growth medium. Cells were cultured in synthetic media which contained varying trace amounts of the elements manganese, iron, cobalt, copper, zinc and molybdenum. The cellular concentration of the elements potassium, iron, copper and zinc were then determined. It was found that the cell accumulates trace metals at a different rate than they are made available. Deficiencies in zinc could be “induced” in the cell by increasing the concentration of iron, manganese and cobalt; cellular iron deficiencies were observed at larger medium concentrations of zinc, manganese, copper and cobalt. Trace metal uptake by the cell was seen to parallel the utilization by multicellular organisms.
    Additional Material: 12 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 443 (1978), S. 11-18 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: TlPd3O4 and TlPt3O4 - Ternary Platinum Metal Oxides with Cluster StructureThe crystal structure of the cardinal red oxide TlPd3O4, prepared by the reaction of Pdo with TlNO3 or Tl2O3 at 550°C, has been determined on powder samples by X-ray and neutron diffraction. The structure of the cubic compound (a = 959.6(2) pm; space group Fm3m; Z = 8) contains square-planar PdO4 units which are joined to a three dimensional skeleton by triply bonding oxygen atoms. The cubic and rhombicuboctahedral spaces are occupied by TlIII and TlI cations so that the compound can be formulated as a mixed valency thallium(III)-thallium(I)-oxopalladate(II). The relationship with the structure of the platinum bronzes is discussed.The analogous ternary platinum oxide TlPt3O4 (a = 966.3(2)pm) has been obtained by thermal decomposition of Tl2Pt2O7.
    Notes: Die Kristallstruktur des durch Umsetzung von Pdo mit TlNO3 bzw. Tl2O3 bei 550°C erhaltenen kardinalroten Oxides TlPd3O4 wurde durch Röntgen-und Neutronenbeugung an Pulverproben aufgeklärt. In der Struktur der kubischen Verbindung (a = 959,6(2) pm; Raumgruppe Fm3m; Z = 8) sind quadratisch planare Pdo4- Baugruppen über dreibindige O- Atome zu einem dreidimensionalen Netz verknüpft. Die würfelförmigen und rhombendodekaedrischen Hohlräume des Gerüstes sind von TlIII-bzw. TlI-Kationen besetzt, so daß die Verbindung als valenzgemischtes Thallium (III)-thallium(I)-oxopalladat(II) formuliert werden kann. Die Verwandtschaftsverhältnisse zu den Strukturen der Platinbronzen werden diskutiert.Das entsprechende Oxoplatinat TlPt3O4 (a = 966,3(2) pm) konnte durch thermische Zersetzung von Tl2Pt2O7 erhalten werden.
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  • 4
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Vibrational Spectra of Solid, Liquid, and Soluted Metal Polysulphides. II Polysulphides Rb2Sn (n ≥ 4) and Na2S4All compounds have been prepared from the elements in liquid ammonia. Whereas Rb2S4 has no defined composition, the vibrational spectra of Cs2S4 and their structure similar to Na2S4 indicate that Cs2S4 is a well-defined compound in contrast to former suggestions. Rb2S5 and Cs2S6 are the members with the greatest chainlength of their homologe series.While Na2S4 still exists of S42- chains in the melt the other polysulhpides disproportionate to S3- radicals and probably monosulphide. In the melt of Cs2S6, quenched to room temperature, a double branched chain structure, the thio-analogue of dithionite, S2S42-, is suggested. All polysulphides have a mean valence frequency, which is independent of the cation and decreases with increasing chainlength.
    Notes: Alle Verbindungen wurden aus den Elementen im flüssigen Ammoniak dargestellt. Während Rb2S4 keine definierte Zusammensetzung aufweist, zeigen die Schwingungsspektren des Cs2S4 sowie deren ähnliche Struktur mit dem Na2S4, daß Cs2S4 entgegen früheren Annahmen als eigenständige Verbindung auftritt. Rb2S5 und Cs2S6 sind die langkettigsten Glieder ihrer homologen Reihe. Während Na2S4 auch in der Schmelze noch aus S42--Ketten besteht, findet für die anderen Polysulfide eine Disproportionierung in S3--Radikale und wahrscheinlich Monosulfid statt. In der auf Zimmertemperatur abgeschreckten Schmelze des Cs2S6 wird eine zweifach verzweigte Kettenstruktur, ein Thioanaloges des Dithionits, S2S42-, angenommen. Bei allen Polysulfiden gibt es eine mittlere Valenzfrequenz, die unabhängig vom Kation mit steigender Kettenlänge absinkt.
    Additional Material: 12 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 98 (1979), S. 627-635 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The toxicity and extent of growth inhibition produced by chloramphenicol (CAP) in CAPs Chinese hamster cells (line V79-5) was found to be dependent on the type and concentration of hexose in the medium. In high levels of glucose (6.5 mM), cultures of CAPs cells underwent 7-8 population doublings in the presence of 100 μg/ml CAP and viability then dropped rapidly. In contrast, lower concentrations of glucose (1.0 mM) permitted only limited growth (2-3 doublings) in the presence of 100 μg/ml CAP, but the cells remained viable and apparently quiescent for prolonged periods of time. The growth potential of V79-5 cells in CAP appeared specifically dependent on glucose, as mannose and galactose could not substitute for glucose. The toxicity of CAP to these cells seemed to be determined primarily by the number of cell doublings in the presence of the drug.A CAPR derivative of V79-5, designated 5-3, was analyzed in order to determine whether the requirement for glucose for cell growth in the presence of CAP also occurred in cells that were isolated as resistant to the drug. In order to rigorously control the hexose in the medium, some experiments were performed with medium containing dialysed, instead of whole, fetal calf serum. It was seen that the growth of the CAPR line in the presence (but not the absence) of 100 μg/ml CAP was dependent on glucose in the medium. Thus, resistance to CAP in these cells appears to be a conditional state, dependent on glucose for expression. Furthermore, the glucose auxotrophy of these cells in the presence of CAP suggests that CAP is still affecting some activities in cells isolated as CAPR.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 454 (1979), S. 134-144 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cobalt(II) Hydrogenarsenate Monohydrate. Preparation and Crystal StructureCo[H2O|HOAsO3] was prepared by heating of As2O5, CoSO4 · 7 H2O and H2O at 150°C in a sealed tube and investigated by X-rays. The compound crystallizes triclinic, space group P¯1 with a = 786.5, b = 1569.9, c = 671.9 pm, α = 94.25, β = 96.89, γ = 90.28° and Z = 8.The structure contains chains of edge-shared CoO6 octahedra connected by AsO4 tetrahedra forming sheets. Two of such somewhat different sheets built up the whole structure. Based on the charge balance derived from the geometrical data and the IR spectra the occurrence of hydrogen bridges is discussed.
    Notes: Co[H2O|HOAsO3] wurde durch Erhitzen von As2O5, CoSO4 · 7 H2O und H2O auf 150°C im Autoklaven dargestellt und röntgenographisch untersucht. Die Verbindung kristallisiert triklin, Raumgruppe P¯1 mit a = 786,5, b = 1569,9, c = 671,9 pm, α = 94,25, β = 96,89, γ = 90,28° und Z = 8. Die Struktur enthält Ketten aus kantenverknüpften CoO6-Oktaedern, welche über AsO4-Tetraeder zu Schichten verknüpft sind. Zwei solche etwas verschiedenartige Schichten bilden die Gesamtstruktur. Anhand der aus den geometrischen Daten berechneten Ladungsbilanz und der IR-Spektren wird das Auftreten von Wasserstoffbrücken diskutiert.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 678-688 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Carbon-Labelling Studies on the α-Oxocarbene-Oxirene IsomerizationThe photochemical Wolff rearrangement of α-diazoketones (1a - g, 3e - g), labelled with 13C or 12C, in dioxane/water yields carboxylic acids containing the label in the carboxy group and the adjacent carbon atom. This proves that the α-oxocarbenes, formed by photolytic elimination of nitrogen, undergo a carbene-carbene rearrangement via oxygen shift (4 ⇌ 5 ⇌ 6). in some cases to an extent of more than 60%, the degree depending upon the substituents and the irradiation wave-length.  -  For examination of the reaction model (scheme 1), both entry pathways (1 → 4, 3 → 6) to the carbene-oxirene-carbene equilibrium are realized by photolysis of the isomeric labelled α-diazoketones le, f, g / 3e, f, g. An alternative mechanism, whereby the scrambling of the carbon label takes place at the ketene stage, can be excluded.
    Notes: Die photochemische Wolff-Umlagerung der 13C- bzw. l2C-markierten α-Diazoketone (1a-g. 3e-g) in Dioxan/Wasser (13:2) führt zu Carbonsäuren, in denen die Markierung in die Carboxygruppe und das benachbarte Kohlenstoff-Atom eingeht. Dadurch wird belegt, Daß die durch photolytische N2-Eliminierung gebildeten α-Oxocarbene einer Carben-Carben-Umlagerung durch Sauerstoff-Verschiebung unterliegen (4 ⇌ 5 ⇌ 6), die je nach Substituenten und Wellenlänge des Lichtes mehr als 60% ausmachen kann.  -  Zur Untersuchung des Reaktionsmodells (Schema 1) werden beide Zugänge (1 → 4 und 3 → 6) zum Carben-Oxiren-Carben-Gleichgewicht durch Photolyse isomerer, markierter α-Diazoketone (1 e, f, g/3e, f, g) beschritten. Ein alternativer Mechanismus, der die Isotopenverteilung auf der Ketenstufe vorsieht. kann ausgeschlossen werden.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1180-1194 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New 1,3,2,4-DiazadiphosphetidinesThe 1,3,2,4-diazadiphosphetidines 5a-f are easily prepared by the reaction of chlorobis(dialkylamino)phosphanes with sodium bis(trimethylsilyl)amide. Further oxidation reactions by O2, S8, N3Si(CH3)3, and alkyl halides are tested in detail in the case of 5a. As shown by NMR spectroscopy, 5a-f are obtained from synthesis almost exclusively as cis isomers which on thermal treatment form a mixture of cis and trans isomers. Methoiodide adducts 9a-f show this isomerisation as well.
    Notes: Die Reaktion von Chlorbis(dialkylamino)phosphanen mit Natrium-bis(trimethylsilyl)amid eröffnet einen bequemen Weg zu den 1,3,2,4-Diazadiphosphetidinen 5a-f, deren Erst- und Zweitoxidation durch O2,S8, N3Si(CH3)3 und Alkylhalogenide am Beispiel von 5a ausführlicher untersucht wird. 5a-f fallen bei der Darstellung fast ausschließlich als cis-Isomere an, die thermische Behandlung führt  -  wie NMR-spektroskopisch gezeigt wird  -  zu einem cis-trans-Isomerengemisch. Auch die Methoiodide 9a-f zeigen cis-trans-Isomerisierung.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 1655-1658 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2,7-Azadiphosphepines  -  New Phosphorus and Nitrogen Containing Heterocycles1 reacts with 2 moles of 2 to give the bicyclic compound 3 containing the new 1,2,7-azadiphosphepine ring system. Diphosphinoamines 5 can be considered as three-membered segments of the eight-membered ring system 1. Thus the amines 5 react with 2 likewise to give monocyclic 1,2,7-azadiphosphepines 6.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 100 (1979), S. 551-561 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cation loss and hemolysis of various mammalian red cells suspended in isotonic non-electrolyte media were investigated. Sucrose buffered with 10 mM Tris-Hepes, pH 7.4 was used as the non-permeable non-electrolyte. Mammals from which the red cells were derived include the human, guinea pig, rat, rabbit, newborn calf, newborn piglet and pig, all of which contain K as the predominant cation species (HK type) and the dog, cat, sheep and cow, all of which possess Na as the predominant cation species (LK type). Of HK cells, a rapid efflux of K takes place from humans, rats and guinea pigs. Of LK type cells, the dog and cat exhibit an augmented membrane permeability to Na. The governing factors which influence cation permeability are the change in pH, temperature, and ionic strength. In response to increase in pH, the red cells of humans, dogs and cats become more permeable to cations, whereas the red cells of rat and rabbit are unaffected. In response to increase in temperature, HK type cells exhibit augmented K efflux, while the Na loss from the dog and cat cells manifest a well-defined maximum at near 37°C. In all cases, a small substitution of sucrose by an equal number of osmoles of salts results in a dramatic decrease in cation loss. By contrast, the red cells of the rabbit, newborn calf, adult cow, newborn piglet, adult pig and sheep display no discernible increase in ion-permeability under the conditions alluded to above. In some species including the newborn calf, dog and cat, an extensive hemolysis occurs usually within an hour in isotonic buffered sucrose solution. The osmolarity of sucrose solution affects these cells differently in that as the osmolarity increases from 200-500 mM, hemolytic rates of the calf and dog reach a saturation near 300 mM sucrose, whereas the hemolytic rate of the cat decreases progressively. Common features pertaining to this hemolysis are (1) the intracellular alkalinization process; and (2) the diminution of the cell volume which take place prior to and onset of hemolysis. SITS, a potent anion transport inhibitor, completely protects the cells from hemolysis by inhibiting chloride flux and the concomitant rise in intracellular pH.
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