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  • Articles: DFG German National Licenses  (2)
  • glass transition temperature  (1)
  • intermolecular correlations  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2667-2681 
    ISSN: 0887-6266
    Keywords: nonradiative energy transfer ; polymer blends ; intermolecular correlations ; miscibility ; phase separation ; modeling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical analysis has been developed to predict fluorescence nonradiative energy transfer (NBET) behavior in homogeneous and phase-separated polymer blends. Conditions where intermolecular correlations need to be included are examined by first investigating the effect of including intermolecular correlations in predictions of NRET behavior in donor and trap (acceptor) end-labeled polymer melts. Donor fluorescence decays and energy transfer efficiencies are predicted for several different polymer systems using donor-trap intermolecular correlations in the theoretical analysis. These results are compared quantitatively to the same predictions recalculated without correlations and demonstrate the need to consider the effects of correlations when analyzing NRET measurements used for quantitative study of phase behavior. For the nonradiative energy transfer systems investigated here, correlation effects can often result in substantial differences, up to 60% as compared to the uncorrelated case, in predictions of relative energy transfer efficiency for bulk polymer. In the case of the blends, the effect of including intermolecular correlations is strongly a function of composition. A two-phase model is proposed to establish a quantitative method for relating energy transfer efficiency to phase-separated blend composition, and it is demonstrated that significant errors in interpretation of experimental NRET data may result if correlation effects are not included. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2987-2997 
    ISSN: 0887-6266
    Keywords: small molecule diffusion ; fluorescence nonradiative energy transfer ; glass transition temperature ; rubbery polymer ; probe shape effects ; probe flexibility effects ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel experimental approach involving fluorescence nonradiative energy transfer (NRET) is employed to study the Fickian diffusion of small molecules in rubbery poly(isobutyl methacrylate) (PiBMA) films near the glass transition, using a formalism that directly relates the small molecule translational diffusion coefficient, D, to changes in the normalized nonradiative energy transfer efficiency, EN. Values of D for pyrene, 1,3-bis-(1-pyrene) propane (BPP), 1,3-bis-(1-pyrene) decane (BPD), 9,10-bis-phenyl ethynyl anthracene (BPEA), diphenyl Disperse Red 4 (DPDR4), and decacyclene in PiBMA are measured over temperatures ranging from approximately Tg to Tg + 25°C. Among these chromophores, significant differences in both the magnitude and temperature dependence of D are observed which are attributed to differences in molecule shape and flexibility, as well as molar volume. Other factors being equal, chromophore flexibility was shown both to increase the magnitude of D and to decrease its dependence on temperature, as does an increase in aspect ratio. For BPD, these effects are attributed to the ability of the flexible molecule to diffuse in a piecewise manner, requiring the cooperative mobility of fewer polymer chain segments than a rigid molecule of the same molar volume. For BPEA and DPDR4, this deviation from D being dominated by molar volume effects is attributed the to high aspect ratio of these elongated molecules. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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