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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(L-valine) (PLV) belongs to the class of polyamino acids having a bulky side chain. It preferably adopts the β-sheet conformation, although high molecular weight PLV may form an α-helix as well. In the present article we report a detailed study of the phonons and their dispersion for β-PLV and the spectra of oligovalines in relation to its polymeric form. The N-deuterated analogue of β-PLV has also been studied to check the correctness of assignments and force field. Density of states and heat capacity have been obtained. The heat capacity is in very good agreement with the experimental measurements of Roles et al. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2281-2292 
    ISSN: 0887-6266
    Keywords: conformation ; phonon dispersion ; α-helix ; normal modes ; poly(L-leucine) ; density of states ; heat capacity ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(L-methionine) (PMet) is one of the two sulfur containing polyamino acids. Raman, FTIR spectra, and heat capacity measurements of PMet have been well interpreted through the normal mode analysis and the density of states derived therefrom. Earlier interpretation of heat capacity data is limited because it is based on the Tarasov model, wherein the concept of group frequency and skeletal similarity are used. A special feature of some dispersion curves is their tendency to bunch in the neighborhood of the helix angle. This has been attributed to the presence of strong intramolecular interactions. Repulsion between the dispersion curves is also observed. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2281-2292, 1997
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 125-139 
    ISSN: 0887-6266
    Keywords: poly-4-methyl-entene-1 ; PT phase diagram ; amorphization under pressure ; disordering on cooling ; thermodynamic anomalies ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We report some highly unusual phase behavior, of general implication for condensed matter, on the polymer poly(4-methyl-pentene-1) (P4MP1) induced by changes in pressure and temperature, as observed in situ by x-ray diffraction. Upon increasing pressure beyond a threhold, the polymer, crystalline under ambient conditions, loses its crystalline order isothermally, passing through a continuously varying sequence of mesomorphic states, the process being reversible. This behavior is observed in two widely separated temperature regions, suggesting, for the first time in a single component system, the possibility of reentrant liquid-crystal and amorphous phases. At the upper temperature region (ca. 250°C) there is a consecutive increase and decrease of melting point with pressure. In the lower temperature region (room temperature) the pressure converts the crystal into an amorphous-like glass obviating the need for going through the melt first, and this in a reversible manner. The latter pressure-induced disordered phase converts into crystal on raising the temperature, and reverts to the glassy, disordered phase on lowering the temperature. Some aspects of this behavior have been found quite recently in water-ice and silica but the process of “melting on cooling” has no precedent in any known system. Other unexpected findings include a new pressure-induced modification of P4MP1 with a one-way only entry with temperature, but full reversibility with pressure leading to a triple point in the PT phase diagram. The above highly uncommon results are putting several prevailing preconceptions to test which are being scrutinized. In the course of it some early expectations on general phase behavior, allowing among others for reentrant phases in one component systems, are being invoked as potentially appropriate for certain polymeric systems, if not for condensed matter in general. © 1993 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1213-1228 
    ISSN: 0887-6266
    Keywords: poly(β-benzyl-L-aspartate) ; conformation ; left-handed ; α helix ; bunching ; crossover ; repulsion ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(β-benzyl-L-aspartate) (PBLA) is an unusual polypeptide, which is capable of going into four different conformations, namely, left-handed α helix, right-handed α helix, ω helix, and β pleated sheet. The present work is a complete study of normal modes and their dispersion in the unusual left-handed α form. A special feature of some of the dispersion curves is their tendency to bunch in the neighborhood of helix angle. This is attributed to the presence of strong intramolecular interactions. Crossing and repulsion between the dispersion curves is also observed. The N-deuterated analogue of PBLA has been studied to check the validity of assignments and force field (Urey Bradley). Specific heat has been obtained from dispersion curves via density of states. A comparative study of left-handed and right-handed forms is presented. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 1179-1182 
    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: Ethylene oxide and propylene oxide have been copolymerized at low temperatures in the presence of anhydrous potassium hydroxide. The monomer reactivity ratios were found to be r(ethylene oxide) = 6.5 and r(propylene oxide) = 0.5.
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 50 (1961), S. 72-82 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurde die mit γ,γ′-Azo-γ-cyan-n-valeriansäure initiierte Polymerisation von Styrol bei 100°C in Dimethylformamid untersucht. Die Polymerisationsgeschwindigkeit ist proportional der Wurzel der Initiatorkonzentration und der Potenz 3/2 der Monomerenkonzentration. Die Übertragungskonstante für das Styrolradikal und Dimethylformamid betrug bei 100°C Cs = 1,08 · 10-4.In Gegenwart des genannten Azo-Initiators wurden unter verschiedenen Bedingungen niedrigmolekulare Polystyrole hergestellt. Ihr Molekulargewicht war osmotisch nicht mehr meßbar und wurde an fraktionierten und unfraktionierten Proben durch Viskositätsmessungen und Endgruppentitrationen ermittelt. Die Ergebnisse werden mit denen anderer Autoren verglichen.
    Notes: The polymerization of styrene using γ,γ′-azo (γ-cyano-n-valeric acid) as initiator was studied at 100°C. in DMF solution.It has been shown that the rate of polymerization is proportional to the square root of the initiator concentration and 3/2 power of the monomer concentration. The chain-transfer constant for styrene radicals and dimethylformamide has been determined at 100°C., with the result Cs = 1.08 · 10-4.Several samples of polystyrene of low molecular weights (below the osmotic pressure range) were prepared under a variety of conditions in the presence of this initiator. Their molecular weights were determined by viscosity and end group titrations, both for fractionated and unfractionated samples. The results are compared with those obtained by other workers.
    Additional Material: 5 Ill.
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