Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Physics  (2)
  • Infrared spectrometry  (1)
  • PACS. 25.70.Mn Projectile and target fragmentation – 21.10.Tg Lifetimes – 27.50.+e 59 ≥ A ≥ 89 – 21.60.Cs Shell model  (1)
Material
Years
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Vibrational Spectroscopy 7 (1994), S. 255-264 
    ISSN: 0924-2031
    Keywords: Fluctuation model ; Hydrogen bonds ; Infrared spectrometry ; Water
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1434-601X
    Keywords: PACS. 25.70.Mn Projectile and target fragmentation – 21.10.Tg Lifetimes – 27.50.+e 59 ≥ A ≥ 89 – 21.60.Cs Shell model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: Decay-spectroscopy study of the 67mFe isomer has been performed at GANIL. This isomer is found to have an energy of 387 keV and a half-life of 75(21) μs. An intermediate excited state is introduced at 367 keV. The results are interpreted in terms of various nuclear models, and a deformed shape is inferred for 67Fe.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 619-638 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic study of the propagation mechanism of the alternating copolymerization of styrene (St) with methyl methacrylate (MMA) in the presence of a complexing agent (diethylaluminum chloride, DEAC) in bulk and in tetrachloroethylene solutions at a molar ratio DEAC/MMA = 0.5 has been carried out. It has been shown that the copolymerization is a chain radical process characterized by a short active-center lifetime, bimolecular termination, and high rate of chain transfer to the complexed MMA. A kinetic scheme has been proposed for the propagation mechanism of alternating copolymerization in the presence of a complexing agent not requiring independent measurements of the equilibrium constant of complexation. It has been found that spontaneous and UV-initiated copolymerizations in the system have different mechanisms of initiation and a common mechanism of propagation. The propagation proceeds by addition of single monomers as well as donor-acceptor complexes of the comonomers to the propagation radicals, with the first mechanism being predominant. Inclusion of the monomers in the complex leads to an increase of the St reactivity and to a decrease of the MMA reactivity in propagation to the corresponding macroradicals in comparison with the reactivity of the free monomers. A number of kinetic and statistical parameters of the propagation reaction have been calculated.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2463-2487 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical copolymerization of butyl methacrylate with 2,3-dimethylbutadiene in the presence of Al(C2H5)2Cl or ZnCl2 results in alternating copolymers. The nature of active centers and the mechanism of polymerization in these systems have been studied by means of ESR measurements in combination with calorimetry at low temperatures. The active centers are monoradicals propagating by alternative addition of single monomer molecules; thus the reaction can be described in terms of a conventional kinetic scheme of radical additional polymerization. Participation of binary donor - acceptor complexes of the monomers in the reaction has not been confirmed. Similar conclusions have been drawn for the other alternating system studied, maleic anhydride-2,3-dimethylbutadiene. The feasibility of formation of alternating copolymers in the studied systems by the conventional mechanism of binary radical copolymerization has been confirmed by qualitative quantum-chemical treatment of the propagation reactions with due account to the donor-acceptor interactions in the transition state.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...