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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 2789-2795 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 1668-1672 
    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
    s.l. : American Chemical Society
    Macromolecules 24 (1991), S. 510-516 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 424 (2003), S. 1010-1010 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Once solely the purview of insects and spiders, the production of silk fibres is now a biotechnological reality. Fibrous silk is used widely, in materials from clothing to carpets to parachutes, so there's a great deal of interest in understanding the precise details of how it forms from silk ...
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 311 (1984), S. 16-16 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] X-RAY structure determinations undertaken so far on different nylons have shown that the chains crystallize in an extended planar zig-zag conformation. In the crystals, the vital amide groups (-NH-CO-) participate in interchain hydrogen-bonding in the plane of the zig-zag, generating ...
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1855-1860 
    ISSN: 0887-624X
    Keywords: helical conformation ; stereospecific polymerization ; isotactic ; polyacetaldehyde ; polytrifluoroacetaldehyde (polyfluoral), polytrichloro-acetaldehyde (polychloral) ; polytribromoacetaldehyde (polybromal) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Minimum potential energy helical conformations for a family of four isotactic polyacetaldehydes have been determined. Our results indicate that all of the polymers form irrational helices. Comparisons have been made with the reported structures for two of these stereoregular polymers based on earlier X-ray diffraction data. c-Axis values associated with the pitch of the helix for polyacetaldehyde and for polytrichloroacetaldehyde (polychloral) were experimentally measured to be 0.48 and 0.51 nm, respectively. Our calculated conformations afforded values for a helix pitch of 0.47 and 0.52 nm, respectively, which derive from a 3.9/1 helix for polyacetaldehyde and a 3.7/1 helix for polychloral. The structure for polytribromoacetaldehyde (polybromal) was predicted to be similar to that for polychloral. For polytrifluoroacetaldehyde (polyfluoral) and polyacetaldehyde, a number of helical conformations with similar energies were found. All of these conformations could be related to the polychloral helical structure. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1855-1860, 1998
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2849-2863 
    ISSN: 0887-6266
    Keywords: nylon oligoamides ; new crystal structure ; morphology ; crystallization ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three-amide oligomers of nylon 6 and nylon 6 6 have been investigated using electron microscopy (imaging and diffraction), X-ray diffraction, and computational modeling. A new crystal structure has been discovered for the three-amide oligomer of nylon 6. This material crystallizes from chloroform/dodecane solutions into an unfolded crystal form that has progressively sheared hydrogen bonding in two directions between polar (unidirectional) chains. This structure is quite different from the usual room temperature α-phase structure of chain-folded nylon 6 crystals, in which alternatingly sheared hydrogen bonding occurs between chains of opposite polarity in only one direction. The occurrence of this new structure illustrates the extent to which progressively sheared hydrogen bonding is preferred over alternatingly sheared hydrogen bonding. Indeed, the progressive hydrogen bonding scheme occurs in the three-amide nylon 6 material even though it requires a disruption to the lowest potential energy all-trans conformation of the chain backbone, and requires all the chains in each hydrogen-bonded layer to be aligned in the same direction. We believe the presence of chain folding, which necessarily incorporates adjacent chains of opposite polarity into the crystal structure, prevents the formation of this new crystal structure in the nylon 6 polymer. In contrast, the three-amide nylon 6 6 crystal structure is analogous to the polymeric nylon 6 6 α-phase structure, found in both fibers and chain-folded crystals, and consists of progressive hydrogen-bonded sheets which stack with a progressive shear. In both structures, the molecules (≈ 3 nm in length) form smectic C-like layers with well-orchestrated stacking of 2.2 nm to form a three-dimensional crystal. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2849-2863, 1998
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2975-2985 
    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: An elongational flow method established in polymer physics was applied to study dynamic structure and properties of biopolymers in solution. Type I collagen solutions in the dilute to semidilute region are studied in elongational flow fields, generated in a Taylor four-roll mill, for temperatures from 20°C through the melting temperature to 60°C. A nonlocalized birefringent signal, characteristic of stiff molecules, is observed at all temperatures. The conformational changes as a function of temperature can be divided into two separate temperature dependent stages. In stage I, at lower temperatures, the collagen molecule behaves as a rigid rod and the birefringent signal Δn rises as a function of increasing strain rate ε. Throughout this stage the type of molecular interaction in semidilute solution does not change but the rate of interaction is increased by thermal excitation. In stage II, a characteristic criticality in the Δn vs. ∊ plot is observed. For strain rates up to a characteristic value, ∊0, the birefringence remains zero and for ∊〉∊0 whole field bright birefringence is observed. The plateau values of birefringence, Δnp, at high strain rates in the Δn vs. ∊ curve decreased with rising temperature in stage II. This criticality in behavior and the decreasing tendency in Δnp with temperature are explained by the collagen molecule changing to a hinged-rod conformation. Thus the untwining of collagen as a function of temperature initiates at several places simultaneously, probably at specific amino acid sequences, within the collagen rodlike molecule.
    Additional Material: 11 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 59 (1996), S. 1389-1394 
    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 response of λ-phage DNA molecules to a well-defined elongational flow field generated by a Taylor four-roller mill was investigated by observing the flow birefringence, Δn. Δn in the center of the four rollers, near the stagnation point, was localized at the mill exit symmetry plane. The intensity gradually increased from the off-symmetrical plane to the center of the mill, and at the exit symmetrical plane, the intensity was maximum. Δn also gradually increases with the strain rate, \documentclass{article}\pagestyle{empty}\begin{document}$\dot \varepsilon$\end{document}. These observations indicate that DNA molecules in the solution would be free draining in nature. From the decay of λn at each point in the mill after a sudden stop of the mill operation at 24 s-1, the rotational diffusion coefficient of molecules, Dr, at each point in the mill space was estimated, where the relaxation time of the decay of λn was considered to be related to the molecular disorienting process. It is concluded that at 24 s-1 λ-phage DNA molecular coils near the stagnation point, which was assumed to be a prolate spheroid as a whole, was so deformed that the aspect ratio p (=b/a ≦ 1, where a and b are, respectively, the longer and shorter axes) would be \documentclass{article}\pagestyle{empty}\begin{document}${\textstyle{1 \over {12}}}$\end{document} of that of the DNA molecule which has just entered the mill space. This result suggests that there is a possibility for the DNA molecule to be in a stretched conformation at a higher strain rate. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 10
    Publication Date: 1992-05-01
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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