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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 2523-2530 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We confirm the existence of a 15 A(ring) period in iodine-doped polyacetylene and provide a new interpretation for this key feature as part of a general model for structural changes during iodine doping. The observed diffraction intensities for different samples suggest the existence of structures with two different types of dopant-containing layers: layers obtained by complete replacement of polyacetylene chains by iodine columns (F layers) and layers obtained by replacement of every other polyacetylene chain by an iodine column (P layers). The F layers in the heavily doped complex alternate with dopant-free layers of polyacetylene chains (U layers), corresponding to a (UF)n stacking sequence. The phase obtained at a lower dopant concentration, which provides the 15 A(ring) spacing, is attributed to a (UPUF)n stacking sequence. At still lower dopant concentrations, one obtains a (UP)n stacking sequence. This model, along with published Raman, Mössbauer, and photoelectron spectroscopy data, suggests that the ratio of I−5 to I−3 increases in going from P layers to F layers. Intense and monotonically decreasing, diffuse x-ray scattering suggests that vacancies of size ∼3 A(ring) are present, probably in iodine columns. A diffuse reflection at 3.1 A(ring), observed in all iodine-doped samples, is due to an average iodine–iodine distance in disordered columnar arrays. On the other hand, ordered arrays of iodine columns in oriented samples give rise to sharp meridional reflections. All ten observed reflections (down to 1.17 A(ring)) in one sample could be indexed based on a 33.8 A(ring) repeat corresponding to (–I−3–I−5–I−3–)n arrays. The observed diffraction pattern was calculated from this model without using any freely adjustable parameters.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 20 (1987), S. 309-316 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 2346-2348 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: X-ray diffraction measurements on all-trans-polyacetylene are consistent with a chain-axis length elongation upon donor doping (+0.026 A(ring) for lithium and +0.04 A(ring) for potassium) and a chain-axis length contraction upon acceptor doping (−0.010 A(ring) for iodine), where the changes refer to the length L of a C2H2 unit (2.457 A(ring) in the undoped polymer). These new experimentally derived results for heavily doped compositions, which ignore possible corrections for cell nonorthogonality in the lithium and iodine complexes, are similar to experimental results for graphite intercalation complexes and are consistent with theoretical predictions for doped polyacetylene. The meridional diffraction lines observed at L and L/2 for potassium-doped polyacetylene indicate that there is no lattice symmetry element which includes a translation operation of L/2 in the chain-axis direction. The observations are consistent with a structural model in which alkali–metal ions with an intracolumn spacing of 4.96 A(ring) are commensurate with the polymer chains for the composition (CHM0.125)x. The likely polymer chain-axis repeat length is 2L (i.e., C4H4) and a lattice symmetry element which includes a translation of L is expected.
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 941-942 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 1261-1267 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 20 (1987), S. 443-445 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 4019-4027 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Polymerization of carbon diselenide, CSe2, at 5 kbar and ∼100 °C has been reported to give a metallic (CSe2)n ladder polymer that superconducts near 6 K at 220 kbar pressure. Using a variety of techniques we find that the material synthesized (showing essentially the same x-ray diffraction pattern as previously published) is not (CSe2)n but instead consists of a mixture of free, trigonal Se and an amorphous C–Se polymeric composition consistent with the formula (CSe0.5)n. Interestingly, possibly as a consequence of staged reactions during synthesis, the Se phase consists of a mixture of large, aggregated crystallites (∼600 A(ring) in diameter) melting at ∼220 °C and nonaggregated small crystallites (∼150–250 A(ring) in diameter) showing a broad melting transition with an endothermic maximum at ∼180 °C. Percolation of the C–Se polymeric composition probably provides the high observed electrical conductivity [σ(300 K)≈10–20 S cm−1 and σ(300 K)/σ (8 K)≈2.5] in the presently available samples. The previously reported high pressure superconductivity is probably associated with the free Se phase in the samples, since selenium is a known superconductor in the 6 K and 220 kbar range.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Incubation of acetates of geraniol, citronellol and linalool with Aspergillus niger resulted in their hydrolysis to corresponding alcohols which were further hydroxylated to their respective 8-hydroxy derivatives. In the case of linalyl acetate, besides linalool and 8-hydroxylinalool, small amounts of geraniol and α-terpineol were also formed. Microsomes (105 000xg sediment) prepared from induced cells of A. niger were found to convert (1-3H)citronellol to 8-hydroxy citronellol in the presence of NADPH and O2. The pH optimum for the hydroxylase was found to be 7.6.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 43-59 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of ethylene and chlorotrifluoroethylene that contain small amounts of units derived from perfluorohexylethylene show improved resistance of thermal stress cracking. This is a consequence of effects of these units on structural parameters of both the crystalline and amorphous phases. Those of the crystalline phase entail growth and organization of lamellae, whereas those of the amorphous phase are related to conformation and packing of polymer chains. The crystalline phase consists exclusively of alternately arranged units of ethylene and chlorotrifluoroethylene. The amorphous phase is characterized by chain segments composed of randomly distributed units derived from ethylene, chlorotrifluoroethylene, pairs of these two units, and units derived from perfluorohexylethylene.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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