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  • Polymer and Materials Science  (5)
  • 2000-2004
  • 1975-1979  (5)
  • 1965-1969
  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(p-vinylbenzophenone), (poly[1-(4-benzoylphenyl)ethylene]), (PVB) has been synthesized for the first time directly from its monomer p-vinylbenzophenone (VB) the preparation of which was improved. In a second step, copolymers containing blocks of photosensitive VB units separated by isolated quenching vinylferrocene (VF) units have been prepared. PVB and the VB-VF copolymers were irradiated in the presence of isopropyl alcohol in benzene solutions. The benzophenone groups inserted in these macromolecular chains obey the same reaction scheme as the photoreduction of the small molecule of benzophenone. However, recombination of the radicals located along the polymeric chain leads to intra- and intermolecular reactions changing drastically the macromolecular morphology by the formation of cycles and networks and by chain scissions. The quantum yields of the photochemical transformations were measured, but they could not be related quantitatively to morphological parameters. In all cases the ferrocene group inhibits strongly the photochemical reaction.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1991-2029 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theory for amorphous orientation in spherulitic polymers is presented based upon a consideration of conformational changes in the chains, loops, and cilia located between crystalline lamellae within a spherulite which is assumed to undergo an affine deformation. Chain statistics are worked out on the basis of (a) an analytical method involving random walks on a cubic lattice between barriers following a technique proposed by DiMarzio and Rubin and (b) a Monte Carlo computer simulation on a tetrahedral lattice. The latter method is considered more appropriate in view of the chain constraints such that lattice geometry becomes important. Values of the amorphous orientation are calculated as a function of the degree of crystallinity, initial lamellar separation, mole fraction of bonds in amorphous chains of each type, and chain lengths of each type of amorphous chain. It is found that tie chains are the principal contributor to amorphous orientation and the amount increases with increasing fraction and decreasing length of these. Results are compared with measurements of amorphous orientation by the birefringence x-ray and the infrared dichroism technique. It is concluded that the tie chains must be initially quite highly elongated and that the assumed affineness of spherulite deformation is not closely obeyed.
    Additional Material: 24 Ill.
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  • 3
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(N-aryl maleimide)s of characteristic structures have been synthesized and some of their physical properties studied. These include N-(2-fluoro phenyl), N-(3-fluoro phenyl), N-(4-fluoro phenyl), N-(2,4-difluoro phenyl), N-(2,5-difluoro phenyl), N-(2,3,5,6-tetrafluoro phenyl), and N-(pentafluoro phenyl). The polymerization of N-(fluoro phenyl) maleimides by free-radical initiation in bulk or in solution and by anionic catalyst have been studied to compare the characteristics of polymerization by γ-ray irradiation with that by free-radical initiation. The polymers were characterized by elemental analysis, intrinsic viscosity, spectroscopy (IR and NMR), programmed thermogravimetric analysis, and x-ray diffraction. Spectra of polymers prepared by radiation and anionic polymerization were nearly identical with those of polymers prepared by free-radical polymerization initiated by AIBN in bulk or in solution and by the self-initiated thermal polymerization. A variety of reaction conditions were tried, but all attempts to change the molecular structure of the polymers were unsuccessful. Rates of thermal degradation for poly[N-(fluoro phenyl) maleimide]s have been analyzed by using a multiple-heating-rate procedure. Overall activation energy, order of reaction, and frequency factor have been evaluated. On the basis of the comparison between the overall activation energy of the thermal degradation of poly[N-(fluoro phenyl) maleimide]s and NMR spectra of their corresponding monomers, it can be concluded that the 1H shifts due to ethylenic protons are so characteristic in sign and magnitude as to be useful in thermal stability elucidation. Some qualitative explanations were given on the stability of these polymers as affected by the type and size of the substituent. The x-ray diffractograms of all samples show two rather broad peaks indicative of noncrystalline structures. The location of the peaks does not depend upon preparation conditions and temperature. Poly(N-maleimide)s of fluoroanilines have not been hitherto described.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 14 (1976), S. 649-652 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 15 (1977), S. 71-75 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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