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  • 2000-2004
  • 1985-1989  (7)
  • 1975-1979
  • 1965-1969
  • 1960-1964
  • 1920-1924
  • 1987  (7)
  • Catalysis
  • Free radicals
Materialart
Erscheinungszeitraum
  • 2000-2004
  • 1985-1989  (7)
  • 1975-1979
  • 1965-1969
  • 1960-1964
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Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Biology and fertility of soils 5 (1987), S. 120-125 
    ISSN: 1432-0789
    Schlagwort(e): Fungal melanins ; Humic acid ; Infrared analysis ; Free radicals
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Geologie und Paläontologie , Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Summary Humic acid-type polymers (melanins) synthesized in culture media by the fungi Aspergillus glaucus, Eurotium echinulatum, Hendersonula toruloidea, Stachybotrys atra and Aspergillus sydowi were analysed for elemental composition, functional group content, infrared (IR) and electron spin resonance (ESR) properties. Results were discussed in comparison with range values referred for soil humic acids. The fungal polymers showed significant differences in carboxyl and nitrogen content and C/H atomic ratios, reflecting a different degree of condensation (aromaticity) among the various samples. IR analysis gave evidence of: (a) the predominant aromatic character of melanins from A. glaucus, E. echinulatum and H. toruloidea; (b) the high content of aliphatic and olefinic components of S. atra melanin; (c) the typical presence of amide bonds in the nitrogen-richest melanins from A. sydowi and H. toruloidea; and (d) the generally low amount of free carboxyl groups, which often appeared involved in hydrogen bonds. ESR spectra showed that all the melanins studied contained appreciable concentrations of organic free radicals of prevailing semiquinonic nature and of the same order of magnitude commonly measured in humic acids from soil and other sources. The free electron concentration was shown to be directly related to the C/H atomic ratio and to the degree of aromaticity shown by IR analysis. This indicated that the highest free radical content in the melanins from E. echinulatum and A. glaucus was associated with the highest presence of condensed aromatic structures. Humic acid-type polymers synthesized by soil fungi may, therefore, contribute to the total free radical content of soil humic substances and play important roles in all reactions involving free radicals in soils and related environments.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    European journal of applied physiology 56 (1987), S. 313-316 
    ISSN: 1439-6327
    Schlagwort(e): Fatigue ; Free radicals ; Lipid peroxidation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The possibility that plasma levels of malonaldehyde (MDA) are altered by exercise has been examined. The presence of MDA has been recognized to reflect peroxidation of lipids resulting from reactions with free radicals. Maximal exercise, eliciting 100% of maximal oxygen consumption ( $$\dot V_{{\text{O}}_{{\text{ 2 max}}} } $$ ) resulted in a 26% increase in plasma MDA (P〈0.005). Short periods of intermittent exercise, the intensity of which was varied, indicated a correlation between lactate and MDA (r 2=0.51) (p〈0.001). Blood lactate concentrations increased throughout this exercise regimen. A significant decrease (10.3%) in plasma MDA occurred at 40% $$\dot V_{{\text{O}}_{{\text{ 2 max}}} } $$ . At 70% $$\dot V_{{\text{O}}_{{\text{ 2 max}}} } $$ plasma MDA was still below resting values, however the trend to an increase in MDA with exercise intensity was evident. At exhaustion, plasma MDA and lactate were significantly greater than at rest. These results suggest, that exhaustive maximal exercise induces free radical generation while short periods of submaximal exercise (i.e. 〈70% $$\dot V_{{\text{O}}_{{\text{ 2 max}}} } $$ ) may inhibit it and lipid peroxidation.
    Materialart: Digitale Medien
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  • 3
    ISSN: 0268-2605
    Schlagwort(e): Hydrosilylation ; Acetylene ; Trichlorosilane ; Silica ; Rhodium ; Ruthenium ; Catalysis ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Gas-phase hydrosilylation of acetylene by tri-chlorosilane catalyzed in a continuous flow apparatus by rhodium and ruthenium phosphine complexes immobilized on the silica via mercapto, phosphine, amine and nitrile ligands has been studied. GLC analysis of the reaction products showed vinyltrichlorosilane to be accompanied by products of double hydrosilylation of acetylene and the redistribution of trichlorosilane followed by the hydrosilylation and hydrogenative hydrosilylation of acetylene with dichlorosilane. A scheme for this complex competitive-consecutive reaction was proposed. The yield and selectivity of vinyltrichlorosilane can be much improved under special reaction conditions, e.g. rate flow of the particular substrates, temperature, given catalyst and others. Kinetic measurements carried out in the range of 115-140°C allowed us to evaluate the activation energy, Ea, for the vinyltrichlorosilane synthesis, which varied between 20.5 and 27.6 kJ mol-1 for the selected rhodium and ruthenium supported complexes.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 190-203 
    ISSN: 0570-0833
    Schlagwort(e): Homogeneous hydrogenation ; Hydrogenation ; Synthetic methods ; Catalysis ; Stereoselectivity ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Stereochemical control is a major concern in the application of homogeneous catalysis to organic chemistry. In this context, the directed hydrogenation of olefins employing cationic rhodium or iridium catalysts has considerable potential, for very high selectivity can be attained under mild reaction conditions. The only requirement is a polar functional group in proximity to the double-bond which remains bound to the metal during the catalytic cycle and thereby controls the Stereochemical course of hydrogen delivery through the constraints of chelation. The substituent is most frequently a hydroxy group OH but can also be an ester, amide or carbamate group; other groups remain to be scrutinized. In cyclic compounds, directed hydrogenation can lead to face-selectivity, and the polar substituent may be in the β-, γ-, or δ-position to the double-bond. Acyclic stereoselection ensues with β- or γ-substituents in appropriate compounds, and the configuration of reduced product is predictable on the basis of simple rules. The application of optically active rhodium complexes leads to useful kinetic resolution procedures.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 309-319 
    ISSN: 0570-0833
    Schlagwort(e): EPR spectroscopy ; Automotive microparticle sources ; X-ray photoelectron spectroscopy ; Environmental chemistry ; Catalysis ; Photoelectron spectroscopy ; Microparticles ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In the last fifteen years the necessity for efficient environmental protection has become generally accepted. However, before practical measures can be taken, a comprehensive assessment of the present environmental situation should be made, taking into consideration the risks involved in as well as the positive effects of any planned environmental changes - whether natural or man made. This clearly calls for close cooperation between the various scientific disciplines. For example, the treatment of exhaust fumes from motor vehicles has been of primary importance in measures taken to restrict the recent damage caused to woodland areas. The introduction of 3-Way-Catalyst technology has been regarded as a viable countermeasure. The following report is intended to describe a method for examining some side effects of catalyst usage. Accordingly, the chemical composition of microparticles emitted from combustion motors through the use of catalysts will be examined and some possible changes in the environment caused by such particles will be briefly considered. As in the area of research into catalysts for industrial synthesis a knowledge of the surface structure of such particles, i.e. the boundary layer between emission product and environment, is necessary in the investigation into their effects. Consequently, a surface sensitive technique from solid state physics, X-ray photoelectron spectroscopy (XPS or ESCA) has found novel use in the area of environmental analysis. In the following report emphasis will be placed on the description of measurement techniques and the interpretation of the results obtained. After a critical consideration of the experimental methods, examples from two different series of measurements on diesel and Otto motors equipped with soot filters or 3-way-catalysts respectively, will be given. Hopefully, this report will also stimulate establishment of the use of EPS in environmental research techniques.
    Zusätzliches Material: 17 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 170-189 
    ISSN: 0570-0833
    Schlagwort(e): Free radicals ; Zwitterions ; Diradicals ; Quantum chemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A knowledge of the geometries at which excited molecules return to the electronic ground state (S0) is essential for the understanding of the structures of photoproducts. Particularly good candidates are geometries corresponding to local minima on the S1 (lowest excited singlet) and T1(lowest triplet) surfaces, as well as S0-S1 conical intersections (funnels). Given sufficient effort, such geometries can nowadays be found numerically for small enough molecules. Still, it is interesting to ask whether more approximate, but also more general, statements can be made concerning the geometries at which the S0 and S1 surfaces closely approach each other. Since many of these are biradicaloid geometries, it is logical to examine the properties of biradicals and related species at some length. After reviewing the two-electron two-orbital model for molecules at biradicaloid geometries, we formulate the conditions under which the S0 and S1 surfaces touch. The results obtained for the simple model are supported by ab initio large-scale configuration interaction (CI) calculations for the twisting of ethylene in the polarizing field of a positive charge and for the twisting of charged double bonds and π-donor-to-π-acceptor single bonds, and by similar calculations for “push-pull” perturbed cyclobutadienes, some of which are predicted to have nearly degenerate S0, S1, and T1 states. The likely consequences of these results for the detailed description of the mechanisms of cis-trans isomerization, the formation of twisted internal charge-transfer (TICT) states, proton translocation, and possibly of the initial step in vision, as well as for the understanding of the regiospecificity of singlet photocycloaddition, are summarized.
    Zusätzliches Material: 16 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 1 (1987), S. 281-284 
    ISSN: 0268-2605
    Schlagwort(e): Catalysis ; Brooke rearrangment ; Iridium ; Palladium ; Platinum ; Complexes ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The complexes [IrH(CO)(PPh3)3], trans-[IrCI(CO)- (PPh3)2], [RhH(PPh3)4], [Pd(PPh3)4], [Pt(trans-stilbene)(PPh3)2] and [Pt(η3-CH2-COCH2)-(PPh3)2] catalyse the rearrangement of Me3SiCH2C(O)CH2Cl to CH2=C(OSiMe3)-CH2Cl.
    Materialart: Digitale Medien
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