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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 293-297 
    ISSN: 0887-6266
    Keywords: poly(p-phenylene) from organometallic polymerization, crystal structure of ; crystal structure of poly(p-phenylene) from organometallic preparation ; X-ray diffraction of organometallically produced poly(p-phenylene) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The two-dimensional crystal structure of poly(p-phenylene) is investigated by linkedatom Rietveld analysis of the x-ray diffraction powder profile. Two molecular chains are packed in a rectangular pgg unit cell (a = 0.779 nm; b = 0.551 nm) with a paracrystalline shift distortion along the chain axis. The molecular conformation is not rigidly planar; rotations between adjacent phenyl-ring planes in a molecule alternate with an angle of about 20°. The setting angle between the mean molecular plane and the a axis is 55.5°.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 957-961 
    ISSN: 0268-2605
    Keywords: rhodium ; cobalt ; polymerization ; allene ; hydrido complex ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organorhodium complexes, such as RhH(PPh3)4, RhH(CO)(PPh3)3, Rh(η3-C3H4Ph)(CO)(PPh3)2, and RhH(dppe)2 [dppe = 1,2-bis(diphenylphosphinoethane)], catalyze polymerization of phenylallene and of 4-methylphenylallene at 60 °C. High-molecular-weight polymers (Mn〉4×105) are isolated from the reaction products by removing the low-molecular-weight (Mn〈3×103) acetone-soluble fraction. The NMR (1H and 13C{1H}) spectra of poly(phenylallene) (1) and poly(4-methylphenylallene) (2) show the structure formed through selective 2,3-polymerization of the monomers, while similarly obtained poly(2-naphthylallene) (3) is characterized only by 1H NMR spectroscopy due to its low solubility in common organic solvents. 4-Fluorophenylallene and 4-(trifluoromethyl)-phenylallene do not polymerize under similar conditions in the presence of RhH(PPh3)4 catalyst but are turned into low-molecular-weight oligomers. CoH(N2)(PPh3)3-catalyzed polymerization of phenylallene and 4-methylphenylallene at room temperature gives the corresponding polymers with molecular weights in the range Mn=(9-15)×104, in high yields. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 13 (1978), S. 161-218 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 10 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 1957-1970 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The bacterial copolyesters poly(3-hydroxybutyrate-co-3-hydroxyvalerate) have been successfully commercialized by ICI and are currently being distributed worldwide. Because of their bacterial origin, they are completely biodegradable. This has opened up numerous opportunities to develop new environmentally friendly products. The solid-state extrusion of a series of biodegradable copolyesters (P(3HB-3HV)) was performed in our laboratory with the aim of gaining fundamental understanding about their processability below their melting temperatures. The extrudability windows were found to span the temperature range from 135 to 150°C, depending on the composition of the samples under our experimental setup. The solid-state extrudates were found to exhibit an extra melting endotherm about 15-20°C above their normal melting temperature. This high temperature melting peak increasingly became dominant at lower extrusion temperatures. Wide angle X-ray diffraction studies did not indicate any phase change that might be responsible for this increase in the melting point. Contrary to the expectations, the solid-state extruded samples did not show significant chain orientation along the extrusion direction. This might be a result of fracture of the mass in the barrel into smaller pieces and their randomization during the course of their passage through the die. When the extrusion temperature was raised closer to the melting temperature, the quality of the extrudates was improved, and this was reflected in improvement of their mechanical properties. © 1996 John Wiley & Sons, Inc.
    Additional Material: 15 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 2207-2216 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: To improve oil and water repellency, fluorine-containing block copolymers, which were composed of methyl methacrylate (MMA), glycidyl methacrylate (GMA), and 1H, 1H, 2H, 2H-heptadecafluorodecyl acrylate (PFA), were blended with an epoxy resin. It was expected that a glycidyl group would mesh with the epoxy resin by primary bonding, and the low surface energy fluorocarbon segment would absorb and orient to the exterior to fluorinate the surface. X-ray photoelectron spectroscopy, contact angle, and peel strength of pressure-sensitive adhesives for modified epoxy resin surface were determined. The amount of fluorine obtained via angular-dependent ESCA investigation in the modified resin surfaces increased with the shallowing of the sampling depth. With increasing modifier content, the amount of fluorine in the modified resin surface layer increased, and the critical surface tension of modified resin surfaces and the peel strength of a silicone pressuresensitive adhesive affixed to the modified epoxy resin, decreased. A considerable amount of fluorine in the resin surface modified with GMA-containing block copolymers remained after Soxhlet extraction, whereas in the surface modified with copolymer without GMA, more fluorine was extracted. It was extracted. It was shown that these copolymers were good surface modifiers to improve oil and water repellency. © 1993 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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