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  • 1
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
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  • 2
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Proton magnetic resonance spectra of model dipeptide molecules R1-C′1O1-N2H2-C2αH2αR2-C′2O2-N3H3-R3 in CCl4 solutions exhibit splited signals when investigating on mixtures of L and D enantiomers differing from the racemic composition. The major effect is observed on amide proton signals which are the ones most sensitive to the ratio of aggregation. The stereoselective dimerization of enantiomeric molecules in the so-called C5 conformational state is shown to be responsible for such a phenomenon, the intensity of which depends on the bulkiness of the side chain R2. A theoretical approach is proposed which gives predictions in close agreement with our own experimental findings.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 1437-1446 
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: By use of a polycondensation procedure free of racemization, stereoregular polymethionines have been synthesized from C-activated D-methionyl-L-methionine and L-methionyl-D-methionyl-L-methionine.The poly(D-methionyl-L-methionine) and poly(L-methionyl-D-methionyl-L-methionine) so prepared are soluble in chloroform and can be purified through dissolution in this solvent and precipitation by ligroin.Poly(D-Met-L-Met)which is obtained in a 25% yield, is about 5000 in average molecular weight. It has no discernible optical activity when examined between 400 and 600 nm in a trifluoroacetic acid solution.Poly(L-Met-D-Met-L-Met) (40% yield, M. W. = 10,000) is an optically active polymer. [α]43624 ≈ + 170° for a chloroformic solution (c = 0.2 CHCl3).
    Materialart: Digitale Medien
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  • 4
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Blends of crystallizable poly(vinyl alcohol) (PVA) and poly-(N-vinyl-2-pyrrolidone) (PVP) of different molecular weights were prepared from aqueous solutions by evaporation and studied by Fourier-transform IR spectroscopy. When the molecular weight of one of the polymer components increases, the PVP content at which crystallinity in PVA is no longer observed decreases. The wide band representing hydroxyl stretching splits into four components at welldefined frequencies which are assigned to (1) multiple hydroxyl-hydroxyl bonding in organized PVA regions, (2) hydroxyls which are simply bonded to carboxyl, (3) hydroxyls doubly bonded to two carbonyls or to one carbonyl and one hydroxyl, and (4) simple hydrogen-hydrogen bonding in amorphous PVA regions. When the PVP content increases, the relative intensity of the bond of di-hydrogen-bonded hydroxyls remains quasi-invariant, while that of multiple hydrogen bonds in PVA decreases, and that of simple hydroxyl-carbonyl bonds increases correspondingly. It appears that the higher the molecular weight, the more effective the hindrance of PVP crystallization. An explanation of the mechanism leading to the formation of different structures in the blends is proposed on the basis of these results. It stresses the importance of the role of chain dynamics in an entangled chain network, which greatly affects the kinetics of crystallization of PVA during the drying step.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 1163-1175 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 4-Methylstyrene (S) was copolymerized with methyl methacrylate (M) or acrylonitrile (A) in benzene or N,N-dimethylformamide solution, respectively. The reactions were carried out at 50°C, using 2,2′-azoisobutyronitrile as free-radical initiator. The copolymer compositions were determined from oxygen (SM) or nitrogen (SA) analysis, 100 MHz 1H NMR, and 25 MHz 13C NMR spectra. These methods lead to the same results. Data plotted according to the Kelen-Tüdős (K-T) procedure indicate that the copolymerization of S with M can be adequately described by the terminal-unit model. The corresponding reactivity ratios (rS = 0,46 ± 0,02 and rM = 0,35 ± 0,02) were in good agreement with literature values and conform with the Q, e-scheme. On the other hand, the K-T plot for copolymerization of the SA system indicates deviations from the terminal model (rS = 0,27 ± 0,02 and rA = 0,10 ± 0,01) in the S- and A-rich regions. This departure was interpreted in terms of penultimate effects on the reactivity of the S- and A-ended radicals. The values of the corresponding reactivity ratios were as follows: rSS = 0,18 ± 0,03, rAS = 0,34 ± 0,04, rAA = 0,06 ± 0,01, and rSA = 0,13 ± 0,01. The theoretical curve of copolymer composition versus monomer feed, calculated with these parameters, is in excellent agreement with the experimental data. This finding shows that, on the basis of the composition data alone, the penultimate model provides an appropriate description of the copolymerization of S and A.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 437-448 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Blends of crystallizable poly(vinyl alcohol) (PVA) with poly(N-vinyl-2-pyrrolidone) (PVP) made from aqueous solutions appear to be miscible in the whole composition range according to DSC results. A large negative value of the interaction parameter between the two polymers was found from melting point depressions. IR spectroscopy evidenced compatibility of the two polymers on a molecular level. DSC, density and IR results all show a proportion of pure PVA crystallites in blends, which decreases with increasing PVP content and becomes nil at about 50 wt.-% of PVP. However, close examination of the hydroxyl stretching region of the blends indicates the presence of organized regions of PVA beyond this limit. According to IR results, the sequence of decreasing hydrogen-bonding power should be the following: multiple hydroxyl-hydroxyl bonding in organized PVA regions, hydroxyl-carbonyl bonding between the two polymers, and simple hydrogen-hydrogen bonding in amorphous PVA regions. It appears that the PVA component can be held in the amorphous state by hydrogen bonding with the PVP component when there is a sufficient amount of the latter in the blend. The amorphous part of PVA is compatible with PVP, but the crystallizable part is not in its most stable form.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 7
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Poly(vinyl alcohol) (PVA) membranes containing small amounts of fixed carboxylate groups were prepared by two methods: reaction with chloroacetic acid in alkaline medium, and polymerization of acrylic acid on radical sites issued from Ce4+ -oxidation of PVA membranes. In the first method, when the reaction was carried out on the dissolved PVA, the crystallinity was greatly reduced, leading to a large increase in permeation flux, a slight decrease in selectivity and a significant increase in the overall performance. The activation energy of permeation was slightly decreased after the reaction. Clear qualitative correlations between different properties were obtained. In the second method, grafting was carried out on the solid membrance and the crystallinity degree was not significantly altered, yet enough to yield membranes with slightly lower selectivity and higher permeability. The Arrhenius plots of permeation rates for some membranes in acetic acid/water mixtures of different compositions showed a transition temperature which is reminiscent of a glass transition temperature the value of which is decreased by the presence of solvent molecules.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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  • 8
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: In three consecutive steps involving halogenation, amination, and condensation with a convenient acyl derivative (1 or 2), α-hydro-ω-hydroxypoly(oxyethylene) (3) was transformed into poly(oxyethylene)s 7 containing 0,6 to 1,3 mol of 3-[3,17β-dihydroxy-1,3,5(10)-estratrien-7α-yl]butyroyl end groups or 0,7 mol of 3-oxo-4-androsten-17β-ylcarboxyl end groups per mol of polymer. Applying the method of affinity partitioning, the former poly(oxyethylene) derivative 7 was used to purify successfully Δ5→4 3-oxosteriod isomerase contained in a crude extract from Pseudomonas Testosteroni.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 1973-1984 
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Poly(vinyl alcohol) (PVA) was studied for use as a basic material for membrane preparation with the aim of dehydrating water-acetic acid mixtures. Membranes of different nature were made by blending a PVA sample of 96% hydroxyl content with a polyacid or a polybase counterpolymer in water, followed by complete evaporation. The PVA-polybase blends gave membranes of low selectivity, unsuitable for dehydration. The membrane M5, made of a 1 : 1 (by wt.) blend of PVA with a special grade of polyhydroxycarboxylic acid (PHC1), presents a good combination of selectivity and permeability. It was studied in a water-acetic acid mixture containing up to 10 wt.-% of water. The Arrhenius-type activation energy for the permeation was found to be 9,0 kcal/mol (38 kJ/mol).
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 10
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Infrared spectroscopy, X-ray diffraction, and nuclear magnetic resonance spectroscopy have been used in investigating the conformation of two stereoregular polymethionines, poly(D-methionyl-L-methionine) and poly(L-methionyl-D-methionyl-L-methionine). When dissolved in a helicogenic solvent, such as chloroform and hexafluoroisopropanol, the polytripeptide is in an α-helical conformation. A helix-to-coil transition can then be induced by addition of trifluoroacetic acid.On the other hand, it appears that the most stable conformation of poly(D-Met-L-Met) is a β antiparallel folded structure in which the linear polypeptide segments are near to the planar extension. This structure has been evidenced through X-ray examination of oriented films, casted from solutions in chloroform. It has also been identified in solution in the same solvent, by use of infrared spectroscopy and by measuring the δHα chemical shift which characterizes the Hα proton in the peptide units. This δHα value is found equal to 5.4 ppm and differs significantly from those which are usually attributed to the α-helical conformation (δHα = 4.2 ppm) and to the random coil (δHα = 4.6 ppm). The β folded conformation of the poly(D-Met-L-Met) appears to be comparatively less stable than the α-helical one for the poly(L-Met) macromolecular stereoisomer since hexafluoroisopropanol is a helicogenic solvent for this last solute and a destabilizing one for the poly(D-Met-L-Met) β folded conformer. X-ray examinations carried out with stretched films, casted from a solution of poly(D-Met-L-Met) in chloroform, result in several data concering the cross β structure of this stereoregular polypeptide in the solid state.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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