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  • Articles  (160)
  • Polymer and Materials Science  (148)
  • Physics  (24)
  • Phylogeny  (12)
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  • Articles  (160)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 24 (1985), S. 427-439 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrostatic effects are believed to determine the molecular structure and function of macromolecules in many ways. In metallo-based enzymes and in metal-macromolecule interactions in solution, these effects may predominate. In order to tackle metal ion-nucleic acid interactions theoretically, we propose a modification of Debye's distance-dependent dielectric function first proposed more than 50 years ago. This function more closely approximates physical reality at small interatomic separations. Our theory yields a dielectric function that gives reasonable agreement with experimental data in preliminary calculations.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dendritic polymers are highly branched structures with globular shape and high number of functionalities. In a divergent or convergent stepwise synthesis perfect macromolecules with controlled size and architecture are obtained. From the broad variety of dendrimer structures some examples are given and the properties of these unusual polymers are illustrated. For comparison the hyperbranched polymers, dendritic structures with defects made in a one-pot polycondensation reaction, are discussed. Differences and conformities of properties like molecular weight distributions, functionalities, solubility, viscosity behavior and glass transition temperatures for both globular polymer structures are explained.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 176 (1975), S. 501-506 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 13 (1969), S. 2073-2084 
    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 pyrolysis of acrylic fiber up to 400°C in an inert atmosphere at 1° and 6°C/min was studied by means of thermogravimetric and differential thermal analysis. The exothermic reaction occuring at 180-300°C was shown to be due to the reaction of nitrile groups by comparing the extent of exotherm with the number of nitrile groups present, determined by infrared spectroscopy. In addition, results of single-fiber tensile measurements, density, and elemental analysis of the pyrolyzed fibers are interpreted in terms of possible molecular structures. The gases evolved on pyrolysis were analyzed for both ammonia and hydrogen cyanide and the liberation of ammonia was attributed to a termination reaction of the polymerization of nitrile groups. The critical conditions necessary for the production of high strength and modulus carbon fiber are discussed briefly in ralation to the chemical changes occurring on pyrolysis.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 45-56 
    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 argument is presented that a primary determinant for polymer ignition is the rate of heat input during thermal decomposition. An experimental protocol is described in which a conventional thermogravimetric analyzer is used to monitor the behavior of polymeric solids brought to ignition by exposure to preheated air. The data obtained are used to establish the minimum heating rate required for ignition and the initial decomposition temperature at that critical rate. These two properties are then combined to give a numerical ranking value which seems to be a reasonable indicator of a material's ignitability hazard potential. Data for a variety of polymers and mixed systems are presented.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 601-629 
    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: A series of four TDI-polypropylene oxide (PO) water-blown flexible polyurethane foams was produced in which the water content was varied from 2 to 5 pph at a constant isocyanate index of 110. A portion of each foam was thermally compression molded into a plaque. The morphology of both the foams and plaques was investigated using dynamic mechanical spectroscopy (DMS), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), scanning electron microscopy (SEM), swelling, wide angle X-ray scattering (WAXS), and small angle X-ray scattering (SAXS). A high degree of microphase separation occurs in these foams, and its degree is nearly independent of water (hard segment) content. In the foam with the lowest water content the morphology possesses many similarities to that of typical linear segmented urethane elastomers. Small hard segment domains are present with a correlation distance of about 7.0 nm. When the water content is increased a binodal distribution of hard segment material appears. There are the small hard segment domains typical of segmented urethane elastomers as well as larger “hard aggregates” greater than 100 nm in size. The larger domains are thought to be aggregates of rich polyurea that develop by precipitation during the foaming reaction. WAXS patterns of the foams suggest urea and possibly hard segment ordering that may be of a paracrystalline nature but certainly lacking in true 3-dimensional crystallinity.
    Additional Material: 15 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 27 (1989), S. 253-258 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 157-163 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From data in the literature on relative rates of copolymerization it has been possible to evaluate two constants, Q and e, characteristic of an individual monomer, which appear to account satisfactorily for its behavior in copolymerization. The constant Q describes the “general monomer reactivity” and is apparently related to possibilities for stabilization in a radical adduct. The constant e takes account of polar factors influencing copolymerization.
    Additional Material: 5 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 48 (1998), S. 181-195 
    ISSN: 0006-3525
    Keywords: protein-RNA complexes ; protein-RNA recognition ; U1A protein ; MS2 coat protein ; U2B″ protein ; synthetase-tRNA complex ; HIV-1 nucleocapsid protein ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The x-ray structure of the glutamine aminoacyl tRNA synthetase bound to its cognate tRNAGln and ATP was reported by Steitz and co-workers in 1989, providing the first high resolution structure of a protein-RNA complex. Since then, high resolution structures have been reported for RNA complexes with five other tRNA synthetases, the elongation factor Tu, the bacteriophage MS2 coat protein, the human spliceosomal U1A and U2B″-U1A′ proteins, and the HIV-1 nucleocapsid protein. Although the number of high resolution structures of protein-RNA complexes are rather small, some general themes have begun to emerge regarding the nature and mechanisms of protein-RNA recognition. © 1999 John Wiley & Sons, Inc. Biopoly 48: 181-195, 1998
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 1107-1131 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the coil-to-helix transition of (dG-dC)3 in M NaCl, 45 mM sodium cacodylate, pH 7, were measured in H2O, D2O, 10 mol % ethanol, 10 mol % urea, and 10 mol % glycerol. At 43°C in H2O the recombination rate is 1.3 ± 0.2 × 107 M-1 s-1; the dissociation rate is 68 ± 10 s-1. The destabilization of the helix in 10 mol % ethanol and 10 mol % urea relative to water is primarily due to a large increase in the helix-dissociation rate. In 10 mol % glycerol, the destabilization of the helix is due to a decrease in the recombination rate and an increase in the dissociation rate. Above 20°C, two exponential decays longer than 1 μs are observed after a temperature jump. The slower relaxation time is 4-10 times faster than the bimolecular component and is independent of oligomer concentration. We attribute this relaxation to a rapid equilibrium between two helical states. At low temperatures and oligomer concentrations of 1 mM or greater, the helices aggregate in 1M NaCl. Experimental data are presented under conditions where aggregation is unimportant and evidence is given that the ΔH-determined spectroscopically is unaffected by aggregation.
    Additional Material: 12 Ill.
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