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  • 1
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Hydrogenase ; Hydrogen Evolution ; Nitrogenase ; Nitrogen Fixation ; Inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Nitrogen-fixingAnabaena cylindrica cells are found to evolve hydrogen in high quantities in the presence of CO plus C2H2. Studies with the inhibitors dichlorophenyldimethylurea (DCMU), disalicylidenepropanediamine (DSPD), dibromothymoquinone (DBMIB), undecylbenzimidazole (UDB) and chloro-carbonyl-cyanide-phenylhydrazone (CCCP) and also withAnabaena grown on nitrate- and ammonia-nitrogen show that the H2-formation is due to the ATP-dependent H3O+-reduction catalysed by nitrogenase. In control experiments CO plus C2H2 inhibited the activities of a cell-free hydrogenase fromClostridium pasteurianum. It is concluded that Anabaena has a hydrogenase whose natural function is to recycle the H2 lost by the action of nitrogenase.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 118 (1978), S. 177-184 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Knallgas reaction ; Hydrogenase ; Hydrogen utilization ; Nitrogenase ; Nitrogen fixation ; Isolated heterocysts ; Anabaena cylindrica ; Nostoc muscorum ; Anabaena variabilis ; Anacystis nidulans ; Cyanophora paradoxa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Several blue-green algae were surveyed for the occurrence of the hydrogenase which was assayed by the oxyhydrogen or Knallgas reaction in the intact organisms. In aerobically grown cultures, the reaction was detectable in Anabaena cylindrica, Nostoc muscorum and in two Anabaena variabilis species, whereas virtually no activity was observed in Anacystis nidulans and Cyanophora paradoxa. In these latter two algae, the reaction was, however, found after growth under molecular hydrogen for several days, which drastically increased the activity levels with all the algae tested. In the nitrogen fixing species, the activity of the Knallgas reaction was enhanced when all combined nitrogen was omitted from the media. H2 and hydrogenase could not significantly support the CO2-fixation in photoreduction experiments with all blue-green algae investigated here. Hydrogenase was assayed by the dithionite and methyl viologen dependent evolution of hydrogen and was found to be present with essentially the same specific activity levels in preparations of both heterocysts and vegetative cells from Anabaena cylindrica. Na2S2O4 as well as H2 supported the C2H2-reduction of the isolated heterocysts. The H2-dependent C2H2-reduction did not require the presence of oxygen but was strictly light-dependent where H2 served as an electron donor to photosystem I of these cells. It is concluded that hydrogen can be utilized by two different pathways in blue-green algae.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 114 (1977), S. 43-49 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Anabaena ; Hydrogenase ; Hydrogen-uptake ; Nitrogenase ; Nitrogen fixation ; Protection mechanism ; Inhibitors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The blue-green alga Anabaena cylindrica is found to consume molecular hydrogen in a hydrogenase dependent reaction. This hydrogen uptake proceeds in the dark and is strictly dependent on oxygen, thus representing a Knallgas reactions. Its rate is almost as high as that of the endogenous respiration in Anabaena. Studies with inhibitors reveal that hydrogen is utilized via the complete respiratory chain providing additional energy for the alga. CO plus C2H2 completely block the Knallgas reaction which explains the previously reported considerable increase in the total H2 formation representing the difference between the nitrogenase-dependent H2-evolution and the reutilization of the gas catalysed by the hydrogenase in intact Anabaena. H2 is able to support the C2H2-reduction in the dark in a reaction again strictly dependent on oxygen. Moreover, H2 is also consumed in experiments carried out under far red light and in the presence of dichlorophenyl-dimenthyl-urea (DCMU) where the energy for nitrogen fixation is no longer provided by respiration but by cyclic photophosphorylation. Under these conditions, H2 is found to supply electrons for the formation of C2H4 from C2H2 in a reaction no longer dependent on the presence of oxygen. Moreover, in these experiments, the presence of H2 stabilizes the C2H2-reduction activity against the deleterious effect of oxygen. Thus, this communication provides evidence for a triplicate function of the H2-uptake catalysed by hydrogenase in intact Anabaena which is (a) to provide energy by the Knallgas reaction, (b) to supply reducing equivalents for nitrogenase, (c) to protect nitrogenase from damage by oxygen.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 587-590 
    ISSN: 0009-2940
    Keywords: [1.1.1]Propellanes, substituted ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis (up to the 10-g scale) and purification of alkyl- and methoxyalkyl-substituted [1.1.1]propellanes are described.
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 6 (1984), S. 211-226 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: By partial sulfonation, desulfonation and ion exchange polytsyrene sulfonic acid resins were synthesized having the same capacity (1.3 milliequivalents/g). By the variation of the preparation methods, however, the distribution of the acid groups within the resins could be changed in a defined way so that different concentration profiles were obtained. It is shown that the properties and reaction behavior of the polymeric resins are determined to a large extent by the local concentration of the functional groups.
    Additional Material: 13 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 192 (1991), S. 2497-2519 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: [1.1.1]Propellanes are introduced to polymer chemistry as a new class of highly reactive monomers which polymerize regiospecifically with breaking of the central CC σ-bond. These rather unique hydrocarbon monomers undergo ring-opening polymerizations with formation of both homo- and copolymers and, in addition, can be used as starting materials for classical poly-condensation chemistry. A wide variety of new polymers is presented all of which contain the bicyclo[1.1.1]pentane fragment, a linearly connecting, rigid unit. This article focusses on questions related to synthesis and structure elucidation.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 26 (1995), S. 241-250 
    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: Long-term High Cycle Fatigue Behaviour at Temperatures in the Creep Range - Investigation of the Correlation with Creep Rupture Properties and Effect of Superimposed Low Cycle Fatigue LoadingThe long-term high cycle fatigue behaviour of the martensitic steel X 22 CrMoV 12 1 and the Ni-base superalloy IN 792 has been investigated. For that purpose, the influence of the ratio of static mean stress to HCF stress amplitude was examined. In addition, the influence of notches on the long-term HCF endurance has been determined. The HCF data can be correlated with creep rupture data by a combination of the method of Keil and Maier and of the Moore-Kommers-Jasper-diagram, additionally, interpolations for any ratio of static mean stress to HCF stress amplitude can be performed. That means, that it will be possible in certain cases to replace costly long-term HCF tests by short-term tests at higher temperature. The superposition of HCF and LCF loading leads to lifetime reductions, which can be explained by simple damage accumulation rules only for small HCF stress amplitudes.
    Notes: Für den martensitischen Stahl X 22 CrMoV 12 1 und die Nickelbasislegierung IN 792 wurde das Anrißverhalten im hochzyklischen Bereich für lange Zeiten ermittelt. Dazu wurde der Einfluß des Verhältnisses von statischer Mittelspannung zur HCF-Schwingungsamplitude untersucht. Weiterhin wurde der Einfluß von Kerben auf die Langzeitschwingfestigkeit bestimmt. Durch eine Kombination des Verfahrens von Keil und Maier und dem Moore-Kommers-Jasper-Diagramm läßt sich eine Korrelation zwischen HCF- und Zeitstanddaten herstellen und zusätzlich können auch Interpolationen für beliebige Verhältnisse von statischer Mittelspannung zu HCF-Schwingungsamplitude durchgeführt werden, wodurch Künftig aufwendige Langzeit-HCF-Versuche in bestimmten Fällen durch kürzer laufende Versuche bei höherer Temperatur ersetzbar sind. Die Überlagerung von HCF-und LCF-Belastung führt zu Lebensdauerverringerungen, die im allgemeinen nur bei kleineren HCF-Schwingbreiten durch einfache lineare Schadensakkumulationsregeln erklärt werden kann.
    Additional Material: 21 Ill.
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  • 8
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1259-1269 
    ISSN: 1434-1948
    Keywords: Metal dithiolenes ; Charge-transfer complexes ; Azo compounds ; Electrical conductivity ; High-resolution X-ray powder diffractometry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Combination of the planar redox-active ions [ML2]2- (L = mnt2- = maleonitrile-1,2- dithiolate; M = Ni (1), Pd (2), Pt (3); dmit2- = 2-thioxo-1,3-dithiol-4,5-dithiolate: M = Ni (4), Pd (5) and trans-4,4′-azobis(1-methyl-pyridinium), (a2+) affords 1:1 ion pairs exhibiting partial and complete electron transfer as evidenced by UV-Vis and EPR spectra. Replacement of planar a2+ by a non-planar dipyridinium ketone b2+ leads to the complexes 1b and 4b. 1a, 2a, and 3a are predominantly composed of dications and dianions while 4a, 5a, and 4b are rare examples of ion pairs consisting of two radical ions. Single crystal X-ray structural analyses was performed on 4a, a(PF6)2, and a(MeSO4)2 while the structure of 1a was resolved by powder X-ray diffractometry. The latter consists of mixed stacks of planar dianions and dications forming a slipped arrangement with the centers of the two ions displaced relative to each other by 250 pm. The short interplanar distances of 340 pm are in agreement with the presence of a weak charge-transfer interaction as indicated by the corresponding absorption band at about 1400 nm. A mean reorganization energy of 0.85 ±0.04 eV is calculated from the Hush equation for complexes 1a, 2a, and 3a. No ion pair charge-transfer band is observable for 4a, 5a, and 4b. Surprisingly, in the solid state structure of 4a the [Ni(dmit)2]- monoanions do not form segregated columns as found in the many ion pairs with redox inert counterions, but prefer a mixed stack arrangement as observed also for 1a.The specific electrical conductivity of pressed powder pellets of complexes exhibiting a charge-transfer band is in the range of 2 × 10-7 to 1 × 10-5 Ω-1cm-1, increasing with increasing driving force of electron transfer in accordance with previous results. Different to that, the conductivity of the other complexes does not depend on driving force and is much higher (2 × 10-4 to 4 × 10-4 Ω-1cm-1).
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 82 (1861), S. 381-384 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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