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  • Polymer and Materials Science  (11)
  • 2020-2024
  • 1985-1989  (11)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1967-1978 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dimethyl phosphonomethylheptamethylcyclotetrasiloxane (II) and 1, 3-bis(dimethyl phosphonomethyl)tetramethyldisiloxane (III) have been prepared by Arbuzov reaction of trimethyl phosphite with bromomethylheptamethylcyclotetrasiloxane (I) and 1, 3-bis(bromomethyl)tetramethyldisiloxane, respectively. Dimethyl phosphonomethylmethylsiloxane dimethylsiloxane copolymers have been prepared by acid-catalyzed ring-opening polymerization of II with hexamethyldisiloxane (MM) as an end-capping reagent and by reaction of II with III as an end-capping reagent. Dimethylsiloxane polymers with dimethyl phosphonomethyldimethylsiloxy end groups have been prepared by acid-catalyzed polymerization of octamethylcyclotetrasiloxane (D4) and III. Under these conditions hydrolysis of the dimethyl phosphonate ester groups was a problem. On the other hand Arbuzov reaction of trimethyl phosphite with bromomethylmethylsiloxane dimethylsiloxane copolymer gave a dimethyl phosphonomethylmethylsiloxane dimethylsiloxane copolymer with uniform properties. These polymers have been characterized by 1H-, 13C-, 29Si-, and 31P-NMR spectroscopy. Their molecular weight distributions have been determined by gel permeation chromatography (GPC) and their thermal stability measured by TGA.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 1499-1514 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A precise method for the determinations of Ti+2, Ti+3 and Ti+4 was developed. The CW-procatalyst before activation contains mostly Ti+4 ions with 6% Ti+3 and 4% Ti+2 ions. Activation with AlEt3 alone at room temperature reduced all the titaniums to lower valence states consisting of 71% Ti+3 and 29% Ti+2. Reduction is incomplete when methyl-p-toluate was present as external Lewis base during activation: at 25°C the distribution of Ti+4 : Ti+3 : Ti+2 is 36% : 25% : 38%; the distribution at 50°C is 37% : 22% : 40%. Aging of the activated catalyst caused little or no changes in the distribution of [Ti+n]; whereas the catalytic activity decays rapidly with aging. The aged catalysts have polymerization activity comparable to the decreased activity of the catalyst during a polymerization. The [Ti+n] was determined for the CW-catalyst during the course of a decene polymerization; they were found to be Ti+4 : Ti+3 : Ti+2 = 30% : 27% : 43%, which did not change with polymerization time. These results suggest that the reducibility of Ti+4 species by AlEt3 or 3AlEt3/MPT to different valence states is predicated by their structures. These species do not undergo further changes in their oxidation states during either aging or polymerization. Their decays probably involve nonreductive metathesis reactions like those known for zirconium alkyls. Possible structures for the stereospecific and nonspecific sites are proposed.
    Additional Material: 4 Ill.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complete sequential assignment of the 1H-nmr resonance frequencies of the active fragment of the rat atrial natriuretic factor (ANF 101-126) has been performed. Two-dimensional nmr techniques have been employed, including phase-sensitive nuclear Overhauser spectroscopy (NOESY), relayed coherence transfer spectroscopy (RELAY), and J-correlated spectroscopy (COSY). Experiments were performed both in D20 and H20 solutions at different pH values. With few exceptions, resonance frequencies were practically pH independent. NOESY spectra were recorded using both 300- and 500-ms mixing times, and no long-range connectivities were observed, leading to the conclusion that ANF 101-126 has no defined secondary nor tertiary structure in water in the pH range used (2.73-5.21).
    Additional Material: 9 Ill.
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Combinations of L- and D-proline residues are useful compounds for finding new structures and properties of cyclic peptides. This is demonstrated with one striking example, the cyclic tetrapeptide c(D-Pro-L-Pro-D-Pro-L-Pro). For this molecule composed of strictly alternating D- and L-configurated residues, a highly symmetrical structure is expected, which should be an optically inactive meso-form. Cyclization of the enantiomeric pure linear precursor D-Pro-L-Pro-D-Pro-L-Pro, however, yields a racemic mixture of two enantiomeric cyclotetrapeptides, both with twofold symmetry and a cis-trans-cis-trans sequence of the peptide bonds. Remarkably, this formation of a racemate was not caused by racemization, but by cis/trans isomerization of all peptide bonds in the ring. This process may occur in the linear precursor during the ring formation (cyclization of conformers with trans-cis-trans or cis-trans-cis arrangement of the amide bonds) as well as in the enantiomeric pure cyclic tetrapeptide at higher temperature. In the latter case, an all-cis structure should exist as the intermediate, which can form a cis-trans-cis-trans sequence in two equivalent ways, leading finally to two enantiomeric cyclotetrapeptides. In the first one, the cis peptide bonds are attributed to the L-residues and the trans peptide bonds to the D-residues; in the second one, the cis bonds belong to the D and the trans bonds to the L-residues. The mixture of these two enantiomers does not crystallize in the racemic form, but in enantiomeric pure separate crystals. The structural properties could be proved by 1H- and 13C-nmr spectroscopy and x-ray analysis. The cis/trans isomerization process was confirmed by optical rotation measurements and CD spectroscopy, as well as DREIDING model studies. Calorimetric measurements in the solid state suggest the existence of the expected all-cis intermediate. The backbone conformation of the 12-membered medium-sized ring shows only slight deviations - up to 6°  - from the planarity of the peptide bonds. On the other hand, the four pyrrolidine rings show different types of puckering of the Cγ or the Cβ atoms.
    Additional Material: 8 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 3399-3411 
    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 azo dye, 2-methyl-N,N-bis(2-hydroxyethyl)-4-aminoazobenzene (nonionic dye) and its conjugate acid (cationic dye) are simultaneously adsorbed by the cellulose membranes carrying sulfonic acid groups from a slightly acidic aqueous solution. Sorption equilibria of the nonionic and the cationic dye are described in terms of the Henry's partition and the ionic exchange mechanism, respectively, in the latter case, the ion exchange constants obtained for the membrane with sulfonic acid group content (SAG) = 261 meq/kg at 30°C are KNaDH = 1.43 × 10-5 and KHDH = 0.542, respectively, where Na, H, and DH refer to sodium, hydrogen, and cationic dye ions. The diffusion coefficients of the nonionic dye (DN) and the cationic dye (DC) in the membranes were estimated from the permeation data of the dyes through the membrane. Both DN and DC decrease with increasing SAG. The ratio DN/DC ranged in 2.2-10, the ratio increases with the SAG.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0009-286X
    Keywords: Baggerschlamm ; Sand ; Abtrennung ; Schwermetalle ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 60 (1988), S. 574-574 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0009-286X
    Keywords: Schwefelwasserstoff-Entfernung ; Schwefel-Erzeugung ; oxidative Schwefelwasserstoff-Wasche ; Sulfolin-Verfahren ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: PC/ABS-blends represent a ternary multicomponent system consisting of bisphenol A-PC, SAN, and a SAN grafted polybutadiene rubber. The morphology of the PC/ABS blends was studied in relation to the PC:SAN composition and the processing melt temperature by means of electron microscopy. The distribution of the rubber particles and the partial miscibility of one thermoplast in the other influences the technological properties of the PC/ABS-blends. The Vicat-Softening temperature depends on the composition of the blends and increases with increasing PC content. For high notched Izod impact strength a certain extent of partial miscibility between PC and SAN and a homogeneous dispersion of the rubber-particles is necessary. The partial miscibility depends on the composition and the processing melt temperature of the blends. With increasing melt temperature a demixing of PC and SAN occurs. The melt temperature has a negligible effect on the notched Izod impact strength on those PC-blends in which the PC-component represents the matrix.
    Notes: PC/ABS-Mischungen stellen ein ternäres Mehrkomponentensystem aus Bisphenol A-PC, SAN und einem SAN gepfropften Polybutadienkautschuk dar. Die Morphologie der PC/ABS-Mischungen wurde in Abhängigkeit vom PC:SAN-Mengenverhältnis und von der Schmelzentemperatur bei der Verarbeitung mit Hilfe der Elektronenmikroskopie untersucht. Der Verteilungszustand der Elastomerkomponente und die partielle Mischbarkeit der Thermoplastkomponenten beeinflussen die technologischen Eigenschaften der PC/ABS-Mischungen. Die Wärmeformbeständigkeit hängt von der Zusammensetzung der Mischungen ab und nimmt mit steigendem PC-Anteil zu. Für ein hohes Kerbschlagzähigkeitsniveau sind eine mit PC angereicherte SAN-Mischphase sowie eine gleichmäßige Dispergierung der Pfropfkautschukpartikel notwendig. Die Mischphasenbildung hängt von der Zusammensetzung und der Verarbeitungstemperatur der Mischungen ab. Steigende Verarbeitungstemperaturen führen zu einer PC/SAN-Entmischung. Der Einfluß der Verarbeitungstemperatur auf die Zähigkeit ist bei denjenigen PC/ABS-Mischungen gering, in denen die PC-Komponente eindeutig die Matrix darstellt.
    Additional Material: 21 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 6 (1985), S. 111-118 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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