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  • 1
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 74 (1999), S. 2749-2751 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The dual nature of (3-(2-(4-(N,N-diethylamino)phenyl)ethenyl)-5,5-dimethyl-1,2-cyclohexenylidene)propanedinitrile (Lemke-e) allows us to write both quasipermanent and erasable holographic gratings in the same storage volume. In the presence of a triplet excited sensitizer, Lemke-e undergoes a photochemical reaction allowing the creation of quasipermanent photochemical holographic gratings. In addition, applying an electric field to the composite allows the storage of erasable photorefractive holograms in the same location as previously stored permanent photochemical holograms. Photochemical gratings (η〉10%) can be written in less than 1 min while photorefractive gratings (η〉50%) can be written in less than 1 s. The photochemical gratings have a dark lifetime of several days. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 901-911 
    ISSN: 0887-6266
    Keywords: activation volume ; relaxation ; pressure ; polymer ; reorientation ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Second harmonic generation (SHG) was used to measure the temperature dependence of the reorientation activation volume of 4-(diethylamino)-4′-nitrotolane (DEANT) in poly(methyl methacrylate) (PMMA). The decay of the SHG signal from films of DEANT/PMMA was recorded at hydrostatic pressures up to 3060 atm and at different temperatures between 25°C below the glass transition temperature to 35°C above it. The activation volume, ΔV*αβ associated with the long range α-type motion of the polymer remained constant at 213 ± 10 Å3 between Tg - 25°C and Tg + 10°C. At higher temperatures, ΔV*αβ decreased linearly with increasing temperature. The activation volume, ΔV*αβ, associated with short range secondary relaxations was constant over the entire temperature range with a value of 77 ± 10 Å3. The data suggest that above Tg chromophore reorientation is coupled to both the long range and local motions of the polymer; whereas, well below Tg chromophore reorientation is closely coupled to the local relaxations of the polymer. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 901-911, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2793-2803 
    ISSN: 0887-6266
    Keywords: activation volume ; relaxation ; pressure ; nonlinear optical polymer ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Second harmonic generation (SHG) was used to measure the temperature dependence of the reorientation activation volume of the side-chain copolymer poly(disperse red 1 methacrylate-co-methyl methacrylate) (DR1-MMA). The decay of the SHG signal from poled films of DR1-MMA was recorded at hydrostatic pressures up to 3060 atm and at different temperatures between 25°C below the glass transition temperature (Tg) to 35°C above it. The activation volume, ΔV*, decreased with increasing temperature. The data suggests that the coupling between chromophore reorientation and the long-range motion of the polymer is stronger for the DR1-MMA side-chain system than in previously measured guest-host systems. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2793-2803, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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