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  • Physics  (69)
  • Organic Chemistry  (30)
  • Occupational Health and Environmental Toxicology  (6)
  • Wiley-Blackwell  (105)
  • 1980-1984  (105)
  • 1940-1944
  • 1982  (105)
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  • Wiley-Blackwell  (105)
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  • 1980-1984  (105)
  • 1940-1944
Year
  • 1
    Electronic Resource
    Electronic Resource
    Über die katalysierte Flüssigphasenoxidation von cis- und trans-Oct-4-enNach einem Vortrag auf der X. Komplexkatalysetagung in Rostock 1980. (1982)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 596-608 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Catalyzed Liquid-Phase Oxidation of cis- and trans-Oct-4-eneThe influences of MoO2(acac)2acac-Acetylacetonat. , MoO 3 and Co(acac) 3 on the liquid-phase oxidation of cis- and trans-oct-4-ene at 110°C were studied. In the presence of molybdenum catalysts the yield of epoxides and the stereoselectivity of epoxide formation are increased. The results are in good agreement with the hypothesis that molybdenum compounds effect only the stereospecific reaction of the hydroperoxides formed with the starting olefin yielding the corresponding epoxide.The cobaltic complex increases the rate of autoxidation, but has no remarkable influence on the yield of epoxides. In the presence of Co(acac)3 more trans-epoxide is formed from cis-oct-4-ene than in the uncatalyzed reaction. This can be explained by an increase of the lifetime of the intermediate peroxyalkyl radical, effected by complex formation of the radical with a cobalt species.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19823240415
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  • 2
    Electronic Resource
    Electronic Resource
    Photochemie adsorbierter Moleküle. VHerrn Prof. Dr. Dr. h. c. H. G. O. Becker zum 60. Geburtstag gewidmet. ESR-Untersuchungen von Phenylkationen bei der Photolyse von Arendiazoniumsalzen im Festkörper und im adsorbierten Zustand (1982)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 209-216 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemistry of Adsorbed Molecules. V. E.S.R.-Investigations of Phenyl Cations during Photolysis of Arendiazonium Salts in the Polycrystalline and the Adsorbed StateDuring photolysis of 4-NR2-substituted arene diazonium salts ground state triplets occur at low temperatures in the e.s.r.-spectra with (π)5(sp2)1 configuration in the polycrystalline as well as in the adsorbed state on SiO2. The influence of anions and the reaction order of decay processes are discussed. The decay of the aryl cations were also investigated in the presence of pyrene as π-electron donor. Reaction takes place with coadsorbed molecules and the decay mechanism changes from ionic character to radical character.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19823240205
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  • 3
    Electronic Resource
    Electronic Resource
    Decomposition of polypropylene hydroperoxide by hindered aminesIssued as NRCC No. 19889. (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 575-582 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hindered amine-induced decomposition of polypropylene hydroperoxide was studied in the solid state and in the presence of a liquid solvent and the polymer was compared with model hydroperoxides. The high reactivity of the macrohydroperoxides appears to be related to the adjacent, hydrogen-bonded hydroperoxide groups that occur in the polymer. The hindered amines are converted to nitroxides in the reaction via hydroxylamine intermediates. Amine-induced decomposition of polypropylene hydroperoxide is faster in the absence of a liquid solvent for the amine than in the presence of the solvent, probably because of the strong amine-hydroperoxide association that occurs in the solid state. The decomposition process in the solid state is sufficiently rapid for the reaction to contribute to the effectiveness of hindered amines in the light stabilization of polymers.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170200231
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  • 4
    Electronic Resource
    Electronic Resource
    Zur Temperatur- und Viskositätsabhängigkeit der Fluoreszenzquantenausbeuten von donator-substituierten 4′-Diphenylphosphinyl-trans-stilbenen in wenig viskosen Lösungsmitteln unterschiedlicher Polarität (1982)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 887-895 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Dependence of Fluorescence Quantum Yields of Donor Substituted 4′-Diphenylphosphinyl trans-Stilbenes on Temperature and Viscosity in Low Viscous Solvents of Different PolarityThe dependence of fluorescence quantum yields of donor substituted 4′-diphenylphosphinyl trans-stilbenes 1 on temperature was investigated between 15-65°C in toluene and n-propanol. It is concluded that the fluorescence quantum yield dependence on temperature is due to the dependence of nonradiative deactivation on solvent viscosity. The nonradiative deactivation is attributed to the ethylene bond rotation in 1. The rotation around the ethylenic bond and the fluorescence are the two most important deactivation processes detected up to now for the first excited singlet of 1 in liquid solution.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19823240604
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  • 5
    Electronic Resource
    Electronic Resource
    Measurement of blood-brain barrier permeation in rats during exposure to 2450-MHz microwaves (1982)
    New York, NY [u.a.] : Wiley-Blackwell
    Bioelectromagnetics 3 (1982), S. 371-383 
    Details
    ISSN: 0197-8462
    Keywords: blood-brain barrier ; rats ; 2450-MHz microwaves ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: Adult rats anesthesized with pentobarbital and injected intravenously with a mixture of [14C]sucrose and [3H]inulin were exposed for 30 min to an environment at an ambient temperature of 22, 30, or 40 °C, or were exposed at 22 °C to 2450-MHz CW microwave radiation at power densities of 0, 10, 20, or 30 mW/cm2. Following exposure, the brain was perfused and sectioned into eight regions, and the radioactivity in each region was counted. The data were analyzed by two methods. First, the data for each of the eight regions and for each of the two radioactive tracers were analyzed by regression analysis for a total of 16 analyses and Bonferroni's Inequality was applied to prevent false positive results from numerous analyses. By this conservative test, no statistically significant increase in permeation was found for either tracer in any brain region of rats exposed to microwaves. Second, a profile analysis was used to test for a general change in tracer uptake across all brain regions. Using this statistical method, a significant increase in permeation was found for sucrose but not for inulin. A correction factor was then derived from the warm-air experiments to correct for the increase in permeation of the brain associated with change in body temperature. This correction factor was applied to the data for the irradiated animals. After correcting the data for thermal effects of the microwave radiation, no significant increase in permeation was found.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bem.2250030309
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  • 6
    Electronic Resource
    Electronic Resource
    A behavioral response of swine to a 60-Hz electric field (1982)
    New York, NY [u.a.] : Wiley-Blackwell
    Bioelectromagnetics 3 (1982), S. 443-451 
    Details
    ISSN: 0197-8462
    Keywords: miniature swine ; ELF ; 60-Hz electric field ; behavior ; Life and Medical Sciences ; Occupational Health and Environmental Toxicology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: It has been shown that rats, given the choice, will spend more time out of a 60-Hz electric field than in it at field strengths ≥ 75 kV/m. This paper describes research to examine the relevance of these data to a different species, the pig. Miniature pigs that had been exposed to a 60-Hz electric field at 30 kV/m for 20 h/day, 7 days/week for as long as 6 months, were tested for their preference for the presence or absence of the field during a 23.5-h period. Similar to earlier results with rats, miniature pigs spent more time out of the electric field than in it during the sleeping period.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bem.2250030407
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  • 7
    Electronic Resource
    Electronic Resource
    Spectroscopic study of rigid-rod polymers. II. Protonation effect (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 509-521 
    Details
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The protonation of a heterocyclic rigid-rod polymer poly(p-phenylene benzbisthiazole) and its model compound has been studied by UV-visible and Raman spectroscopy. Because of the two nitrogens on the heterocyclic ring, spectroscopic features of unprotonated, half-protonated, and fully protonated structures have been identified. For the fully protonated molecule, there is also an increase in conjugation between the phenyl ring and the heterocyclic ring.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.180200312
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  • 8
    Electronic Resource
    Electronic Resource
    Investigation of molecular order in liquid-crystalline solutions of cellulose triacetate using PMR spectroscopy (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 1019-1028 
    Details
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Liquid-crystalline solutions of cellulose triacetate (CTA) in trifluoroacetic acid (TFA)-CH2Cl2, TFA-1.2-dichloroethane (1,2-DCE) solvent mixtures were examined by means of PMR spectroscopy. CTA forms both cholesteric and nematic phases in these solvents depending on the CTA concentration. In cholesteric solutions the CH2Cl2 signal is initially a singlet and then splits into a doublet. The time dependence of the splitting and the effect of CTA concentration are reported. The results suggest that the cholesteric phase slowly changes into a nematic phase in the magnetic field. The splitting of the CH2Cl2 proton signal into a doublet and the 1,2-DCE signal into a quartet are due to direct magnetic dipole-dipole interactions. Rotation of the sample in the magnetic field results in the disappearance of the doublet or quartet and suggests that the solvent molecules are originally oriented in the direction of the magnetic field. In the biphasic region, immediate splitting of the CH2Cl2 proton signal suggests that the anisotropic phase is nematic.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.180200610
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  • 9
    Electronic Resource
    Electronic Resource
    Microphase separation in sulfonated polystyrene ionomers (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 1503-1509 
    Details
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Small- and wide-angle x-ray scattering results for a series of un-neutralized and neutralized sulfonated polystyrenes are presented for the range of sulfonation from 0 to 7.26 mol %. From the small-angle scattering it is shown that above the 3 mol % level for both the zinc and sodium salts, a Bragg spacing (37 Å) and diameter (6.9-8.4 Å) of the scattering unit can be calculated. When the concentration of salt is increased, there is no appreciable change in the latter two measurements. The wide-angle data indicate that the cations do not influence to any large extent the basic intramolecular and intermolecular structure of polystyrene. All the data are consistent with the onset of clustering above a critical ion concentration.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.180200815
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  • 10
    Electronic Resource
    Electronic Resource
    Transition metal ions and amides. VIII.Part VIII, see [1]; Part VI, see [2]. Discrimination between different models for the complexation of Cu2+ with N, N′-diglycyl 1, 2-ethanediamine, N, N′-diglycyl-1, 3-propanediamine and glycine ethylamide by potentiometric or by spectrophotometric titration (1982)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 65 (1982), S. 46-54 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexation of Cue2+ with 1, 8-diamino-3, 6-diaza-2, 7-octanedione (—N, N′-diglycyl-1, 2-ethanediamine, DED) and with 1, 9-diamino-3, 7-diaza-2, 8nonanedione (—N, N′-diglycyl-1, 3-propanediamine, DPD) has been studied by potentiometric and by spectrophotometric titration. With both ligands L the complexation to Cue2+ leads to relatively complicated equilibria with CuLH3+, CuL2+, CuLH-2, and dimeric Cu2L24+ complexes. With DED, another dimeric species, Cu2L2H-22+, is formed in addition. Independent numerical treatment of spectrophotometric and poteritiometric titrations was used to obtain a satisfactory model for the complexation and to test the relative discriminatory power of the two methods. Titrations of glycine ethylamide (GEA) were used as an additional test and as a model for DED and DPD. It was shown that in each case spectrophotometric titrations give results of similar reproducibility and have a discriminatory power equal to or better than potentiometric titrations, provided that optimum mathematical algorithms are used in the numerical treatment.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19820650106
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