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  • 1980-1984  (2)
  • Physical Chemistry  (1)
  • Physics  (1)
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  • 1980-1984  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 35-42 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The first confirmed synthesis of methylene malonamide (MeMal) is reported. This monomer was prepared by the thermal elimination or fluoride-ion-initiated elimination of trimethylsilyl chloride from α-chloro-α(trimethylsilyl-2-methyl) malonamide. Spectral data for the monomer are given. MeMal has been shown to be unstable in a variety of protic organic solvents, including water and alcohols, thus giving the appropriate (α-methyl) substituted malonamides. MeMal is stable in most aprotic solvents.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 845-854 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A preliminary report is given of relative reactive cross sections for four abstraction reactions H + H′Br ← HH′ + Br with attacking atom (A) H or D, and atom under attack (B) H or D. The pattern of reactive cross sections, as obtained in a crossed molecular beam experiment at a collision energy ET = 7 kcal/mol, indicates Sr(D,H) ≤ Sr(D,D) 〉 Sr(H,H) 〉 Sr(H,D). The atoms in parentheses are A and B. We describe a three-dimensional classical trajectory (CT) study on a potential-energy surface proposed in 1969 by Parr and Kuppermann (PK); the CT results are in fair accord with experiment. It is suggested that (D,H) has the largest cross section because it exhibits the most favorable relative timing of A approach to BC rotation. On the basis of CT it appears that the same sequence of cross sections and the same rationale may be applied to the exchange reactions H + BrH′ ← HBr + H′.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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