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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 34 (1969), S. 959-963 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1617-4623
    Keywords: MAP kinase kinase ; Ste7 ; Saccharomyces cerevisiae ; Candida albicans
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The HST7 gene of Candida albicans encodes a protein with structural similarity to MAP kinase kinases. Expression of this gene in Saccharomyces cerevisiae complements disruption of the Ste7 MAP kinase kinase required for both mating in haploid cells and pseudohyphal growth in diploids. However, Hst7 expression does not complement loss of either the Pbs2 (Hog4) MAP kinase kinase required for response to high osmolarity, or loss of the Mkk1 and Mkk2 MAP kinase kinases required for proper cell wall biosynthesis. Intriguingly, HST7 acts as a hyperactive allele of STE7; expression of Hst7 activates the mating pathway even in the absence of upstream signaling components including the Ste7 regulator Ste11, elevates the basal level of the pheromone-inducible FUS1 gene, and amplifies the pseudohyphal growth response in diploid cells. Thus Hst7 appears to be at least partially independent of upstream activators or regulators, but selective in its activity on downstream target MAP kinases. Creation of Hst7/Ste7 hybrid proteins revealed that the C-terminal two-thirds of Hst7, which contains the protein kinase domain, is sufficient to confer this partial independence of upstream activators.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 21 (1991), S. S269 
    ISSN: 1434-6079
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We have calculated final n, l, m-distributions for the electron capture in Na+ + Na(28d) collisions and N5+, Ar8+ + Cs(6s) collisions using a three-body classical trajectory Monte-Carlo (CTMC) method. The collision velocity range is 0.5 ≲ x ≲ 1.7. Here, x = vp/ve, where vp is the ion projectile velocity in the laboratory frame and ve is the initial orbital velocity of the electron bound to the alkali-metal core. The results are discussed along with experimental data.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 27 (1993), S. 295-301 
    ISSN: 1434-6079
    Keywords: 31.10 ; 32.80.D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We investigate how an initially symmetric state of He, made of two identical electron wave packets, can decay by the descent of an electron into a lower orbit and the ionisation of the second electron. Matrix elements of the Green's function are calculated via a non perturbative, mean field approximation. We find examples where the evolution mechanism predicted by the mean field approximation shows a breaking of the symmetry of the initial state and may lead to autoionization. The dominant component of the solution is asymmetric for energies below ≈ −0.005 a.u., but turns out to be symmetric for positive energies.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 7 (1963), S. 959-969 
    ISSN: 0021-8995
    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
    Notes: The initial stages of isotactic polypropylene oxidation were investigated by oxidizing at 130°C. to various extents up to 10 ml. of oxygen consumed per gram of polymer. The development of infrared absorption bands in the carbonyl regions was followed, as increasing amounts of oxidation occurred. The oxidation uptake curves showed that both autocatalytic rate and induction time depended primarily on the thickness of the sample, contrary to the case of polyethylene. This indicated the initiation process was primarily diffusion controlled for samples of the thickness range studied. The presence of copper shortened the induction times and increased the autocatalytic rate. In this case, the dependency of the induction time on thickness was less. Dielectric data showed that polypropylene became unsuitable electrically at about the point where the autocatalytic oxidation set in. It was also found that the effects of prior exposure to oxidative conditions were cumulative to a considerable extent, and thus resulted in shorter induction times.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 2641-2649 
    ISSN: 0021-8995
    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
    Notes: Several samples of polyethylene were exposed to attack by fuming nitric acid and the resulting changes in density, infrared absorption, and visual appearance were recorded. The motivation for this investigation lies in the possibility of using acid etching as a means of studying the structure of interspherulitic regions in polyethylene and the relations between these and structure-sensitive properties such as stress-crack resistance. The results indicate that certain parts of the samples were attacked preferentially by the acid; the residual material, though of a porous gross structure, was of higher density than that of the average initial material. The differences in visual appearance were the most dramatic and appear to correlate with stress-crack resistance. Insofar as quantitative characterization of interspherulitic regions are concerned, the merits of this method of investigation are still in doubt and await further study.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 587-609 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermal oxidation and copper-catalyzed thermal oxidation of polypropylene were studied over a range of elevated temperatures. The apparent activation energy for both of these processes, based on t10 induction periods, was 27 kcal./mole. Measurement of the time (t10) required for interaction of 1 g. of polymer with 10 cc. of oxygen was found to be a convenient and expedient technique for estimating the induction period, since this amount of oxygen is sufficient to cause deterioration of physical and dielectric properties of the polymer. In the absence of copper, stabilization of polypropylene comparable to that achieved with polyethylene was observed when antioxidant concentration was increased proportionately to compensate for the larger number of oxidation-susceptible tertiary carbon atoms in polypropylene. However, it was found that thermal antioxidants, even in high concentration, were ineffective protectants for polypropylene when copper was present. Conventional copper chelators and metal deactivators were, at best, only slightly effective in suppressing oxidation catalyzed by copper and usually were unsatisfactory for a variety of other reasons. Oxamide, however, and particularly its less volatile, high melting, disubstituted derivatives, functioned cooperatively with a wide variety of antioxidant systems and were found to comprise a highly effective and useful family of inhibitors of the copper-catalyzed oxidation of polypropylene.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Saturated hydrocarbons evolved during electron irradiation of polyethylene are characteristic of short side chains in the polymer. A convenient analysis is effected by programmed temperature gas chromatography. In order to minimize the relative concentrations of extraneous hydrocarbons, i.e., those not arising from selective scission of complete side chains, it is necessary to irradiate at low temperatures and doses. Such analyses of a high pressure polyethylene (DYNK) indicates that the two methyls per 100 carbon atoms detected in infrared absorption are probably equal amounts of ethyl and butyl branches. These arise by intramolecular chain transfer during polymerization. At a dose of 10 Mrad about 1/4% of the alkyl groups are removed. Methane is the only hydrocarbon detected on irradiation of polypropylene, indicating little combination of methyl radicals to form ethane during irradiation.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2205-2214 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A stream of atomic oxygen, produced by passing oxygen at low pressure through a radio-frequency coil, was allowed to impinge on films prepared from several dozen different polymers. The flow of oxygen radicals was regulated so that the reaction temperatures were between 40 and 70°C. The rapid reactions which occurred at the polymer film-oxygen radical interface were essentially unaffected by the presence of phenolic antioxidants over a wide range of concentrations but rate of reaction was greatly affected by the structure of the polymer. Bulk properties of the polymers were unchanged because the attack by atomic oxygen is limited to the surface of the polymer. In many instances a simple ablation of the surface was observed, but in some cases, especially polyethylene and polypropylene, a highly oxidized surface layer was created. These oxidized surface layers had remarkably low contact angles with water and should be of great interest in improving adhesion and other surface-dependent properties of polymers.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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