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  • Chemistry  (4)
  • Amino Acid Sequence
  • Base Sequence
  • Inorganic Chemistry
  • 1990-1994  (4)
  • 1992  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2677-2681 
    ISSN: 0887-624X
    Keywords: polystyrene ; photooxidation ; oxygen ; nitrous oxide ; ultraviolet ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Strips of polystyrene held in a flowing O2 or N2O atmosphere have been exposed to 240-600 nm radiation. The extent of photooxidation has been followed by x-ray photoelectron spectroscopy (XPS). Although N2O is a more reactive gas than O2, it produces a less oxidized polymer surface. This surprising observation can be correlated to the photochemistry occurring at the gas/polystyrene interface. © 1992 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Advanced Materials for Optics and Electronics 1 (1992), S. 29-36 
    ISSN: 1057-9257
    Keywords: Gallium-arsenic compounds ; Single-source ; gallium ; arsenide ; precursors ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Reactions of GaX3 (X = Br, I) with As(SiMe3)3 in 1:1 and 2:1 mole ratios were investigated. For the latter reactant stoichiometry, substances having the empirical formulae AsBr3Ga2 (1) and Asl3Ga2 (2), the analogues of the previously reported single-source GaAs precursor (AsCl3Ga2)n, were isolated as yellow isolated as yellow insoluble powders. Low-temperature reactions in a 1:1 mole ratio resulted in the isolation of the adducts Br3Ga.As(SiMe3)3 (3) and I3Ga.As(SiMe3)3 (4). On the other hand, at room temperature the GaBr3 reaction resulted in a complex mixture from which no characterizable compounds were isolated, whereas the Gal3 reaction afforded the crystalline compound [I2GaAs(SiMe3)2]2 (5). The structures of 4 and 5 were elucidated by complete single-crystal X-ray analysis (crystal data: 4, monoclinic, space group P21/c, a = 16.497(2) Å, b = 9.629(1) Å, c = 16.658(2) Å, β = 113.21(1)°, V = 2432(1) Å3, Z = 4; 5, orthorhombic, space group Pbca, a = 14.279(2) Å, b = 17.509(2) Å, c = 13.818(2), Å, V = 3455(1) Å3, Z = 4).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 1043-1053 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the solvolysis of [Co(CN)5Cl]3- ions have been investigated in mixtures formed by the addition of ethane-1,2-diol or ethanonitrile to water where the physical properties indicate little enhancement of structure in water-rich conditions. The effect on the kinetics of this solvolysis of this lack of structural change in the solvent shows in the linearity of the variation of log (rate constant) with the reciprocal of the dielectric constant for the addition of ethane-1,2-diol to water and the absence of any prominent extrema in the enthalpy or entropy of activation using either co-solvent. However, the effect of changes in solvation on the solvolysis with these two co-solvents appears to operate in a similar manner to the effects found when the hydrophobic co-solvent propan-2-ol is added to water. The application of a free energy cycle to the process of the initial state going to the transition state for this dissociative process suggests that, with both co-solvents, [Co(CN)5]2- in the transition state is more stable than [Co(CN)5Cl]3- in the initial state. © John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 563-577 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rates of solvolysis of complex ions [Co(3Rpy)4Cl2]+ with R = Me and Et have been determined in mixtures of water with t-butyl alcohol over a range of temperatures. Extrema found in the enthalpy ΔH* and entropy ΔS* of activation are correlated with the physical properties of the solvent mixtures which are influenced by changes in the solvent structure and these extrema are compared with those found for the solvolysis of related complexes in water + alcohol mixtures. Isokinetic plots over wide ranges of ΔH* and ΔS* are compared for the solvolysis of CoIII complexed to a variety of ligands. The application of a free energy cycle shows that the emergent cobalt (III) cation in the transition state becomes increasingly stabilized in water-rich mixtures relative to the cobalt (III) cation in the initial state as the mol fraction of t-butyl alcohol increases.
    Additional Material: 7 Ill.
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