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  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2987-2997 
    ISSN: 0887-6266
    Schlagwort(e): small molecule diffusion ; fluorescence nonradiative energy transfer ; glass transition temperature ; rubbery polymer ; probe shape effects ; probe flexibility effects ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2625-2635 
    ISSN: 0887-6266
    Schlagwort(e): fluorene ; fluorescence ; quenching ; in situ monitoring ; free-radical polymerization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A new approach for monitoring in situ the progress of an addition polymerization has been developed based on the fluorescence quenching of fluorene. Fluorene is quenched by the enone functionality on acrylates and methacrylates, but is not quenched after the carbon-carbon double bond in this group is broken by incorporation into the polymer backbone. Ethyl (2-fluorenyl)methacrylate was used as a self-quenching comonomer during the 2,2'-pazo bis(2-methylpropionitrile)-initiated free-radical copolymerization of methyl methacrylate at 60°C. The fluorescence intensity increases by 60% up to the onset of the gel effect (defined as the sudden increase in the temperature profile). The system shows sensitivity well into the glassy state, with fluorescence increasing more than two orders of magnitude from the beginning of the reaction. This sensitivity is compared with that of two free-volume-dependent probes, 1,3-bis(1-pyrene)propane and dimethylaminobenzylidenemalononitrile, and to fluorene. The temperature profile of the test-tube-scale reaction was used as an internal reference for characterizing the sensitivity of the probes with respect to the gel effect region. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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