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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1067-1076 
    ISSN: 0887-6266
    Keywords: transmission electron microscopy ; block copolymer ; polyimide ; nanofoam ; porous films ; polymer foam ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transmission electron microscopy was performed on a polymeric nanofoam material, derived from a triblock copolymer composed of a fluorinated polyimide center block, 3F/PMDA (derived from pyromelletic dianhydride (PMDA) and 1,1-bis(4-aminophenyl)-1-phenyl-2,2,2-trifluoroethane (3F)) and polypropylene oxide (PO) end blocks. The cast and imidized polymer exhibits a microphase-separated morphology consisting of PO microdomains within a polyimide matrix. The final nanofoam material is obtained by decomposing PO microdomains into low molecular weight products, which diffuse out of the polyimide matrix leaving nanometer length scale voids. Ruthenium tetroxide staining prior to microscopy was used to enhance the contrast between the 3F/PMDA matrix and the PO microdomains or voids, which permitted a more detailed view of the microstructure of both the foamed and unfoamed materials. From the power spectra of the micrographs, spatial correlation between the PO microdomains in the unfoamed material and between the voids in the foam were found. An interdomain separation distance of ca. 37 nm was observed. Analysis of the image yielded an average area of 411 nm2 for the PO domains. The analysis indicated that the PO domains were oblong, having average major and minor dimensions of 35 and 12.5 nm, respectively. An autocorrelation of the image showed that the domain center of masses were positioned 41 nm apart, in close agreement with the domain spacing (ca. 37 nm) found as described above. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1067-1076, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2723-2729 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mild, efficient method of nitrating olefins was described recently by Corey and Estreicher. Application of their procedure to diene polymers failed because of the insolubility of the hydrophobic polymer in the aqueous nitromercuration regent. Use of water-immiscible organic cosolvents gave slow nitromercuration with substantial formation of nitrite esters. To overcome these problems a nonaqueous phase transfer-assisted method of rapid selective nitromercuration of diene polymers was developed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 1505-1516 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Iodine azide adds to cyclohexene in acetonitrile or 4:1 methylene chloride/acetonitrile to give trans-1-azido-2-iodocyclohexane. In methylene chloride this reaction gives a mixture of the cis-and trans-iodoazides owing to competing radical addition. Iodine azide adds to 1-hexene in acetonitrile by an ionic mechanism to give a 3:1 mixture of the 2-azido-1-azido- and 1-azido-2-iodohexanes. Dehydroiodination of the model iodoazides proceeds smoothly with potassium t-butoxide in diethyl ether or THF in the presence of 5 mol % 18-crown-6 at room temperature, giving in the previous example a mixture of 2-azido- and trans-1-azidohexenes. Polybutadiene, carboxyterminated poly(acrylonitrile-co-butadiene), and hydroxy-terminated polybutadiene gave iodoazide derivatives with up to 96% of the theoretical maximum nitrogen content and strong azide IR absorption. High azidoiodination gave polymer with N3/I ratios slightly higher than unity while low percent azidoiodination led to polymer with N3/I ratios of as low as 2:3. All of the nitrogen introduced was in the form of azide function. Dehydroiodination gave polymers with vinyl azide functionality and caused loss of some of the azide groups. All the azidoiodinated polymers decomposed between 120 and 160°C. The dehydroiodinated materials were less stable, decomposing between 100 and 150°C. The temperature of initial decomposition decreased as azide content increased. Polymers with 〉55-60% of the theoretical maximum azide content were shock sensitive.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2795-2802 
    ISSN: 0887-6266
    Keywords: ultrathin polymer films ; fluorescence nonradiative energy transfer ; second harmonic generation ; polymer relaxation ; small-molecule diffusion ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two optically based, molecular probe techniques are employed to study relaxation and small-molecule translational diffusion in thin and ultrathin (thicknesses 〈 ∼200 nm) polymer films. Second harmonic generation (SHG) is used to study the reorientational dynamics of a nonlinear optical chromophore, Disperse Red 1 (DR1) (previously shown to be an effective probe of α-relaxation dynamics) either covalently attached or freely doped in polymer films. Our studies on films ranging in thickness from 7 nm to 1 μm show little change in Tg with film thickness; however, a substantial broadening of the relaxation distribution is observed as film thickness decreases below approximately 150 nm. Experimental guidelines are given for using fluorescence nonradiative energy transfer (NRET) to study translational diffusion in ultrathin polymer films. Appropriate choice of a fluorescence donor species is important along with ensuring that diffusion is slow enough to be measured appropriately. Initial results on the diffusion of a small-molecule probe, lophine, in poly(isobutyl methacrylate) indicates that there is little change in probe diffusion coefficients in films as thin as 90 nm as compared to bulk films. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2795-2802, 1997
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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