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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 619-626 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mutual precipitates of poly (N, N-dimethyl acrylamide) and poly (4-hydroxystyrene) were collected from dioxane, methanol, or acetone. The glass transition (Tg) temperatures of the precipitates are higher than the weight-average values. Clear films cast from dimethylformamide solutions have lower Tg values. Complexation also occurred between poly (ethyl oxazoline) and poly (4-hydroxystyrene) in dioxane and between poly (vinyl pyrrolidone) and poly (4-hydroxystyrene) in methanol. Again, the glass transition temperatures of the precipitates are higher than the values for the blend films. The ΔCp values associated with the glass transitions of the complexes are smaller than those of the blends having the same compositions. Negative excess heat capacities of mixing have been observed for several precipitates.
    Additional Material: 10 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1481-1490 
    ISSN: 0887-624X
    Keywords: ibuprofen ; ketoprofen ; naproxen ; copolymer reactivity ; thermal stability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three nonsteroidal antiinflammatory drugs, 2-(4-isobutylphenyl)-propionic acid (ibuprofen), 2-(3-benzoylphenyl)-propionic acid (ketoprofen), and 2-(6-methoxy-2-naphthyl)-propionic acid (naproxen), were covalently linked with 2-hydroxyethyl methacrylate (HEMA). The drug-linked HEMA (M1) (ibuprofen-linked HEMA abbreviated as HI; ketoprofen-linked HEMA as HK, and naproxen-linked HEMA as HN), were respectively copolymerized with methacrylic acid (M2), MA, to obtain macromolecular prodrugs. The compositions of the copolymers were determined by means of a 1H-NMR spectroscopy and monomer reactivity ratios were estimated using the Kelen-Tüdös linear differential equation. The reactivity ratios are: r1 = 0.101 ± 0.012, r2 = 1.071 ± 0.065 for HI-MA; r1 = 0.344 ± 0.066, r2 = 0.966 ± 0.032 for HN-MA, and r1 = 0.650 ± 0.182, r2 = 1.032 ± 0.106 for HK-MA, respectively. The monomer reactivity toward to MA radical estimated from 1/r2 values is almost same for all three monomers (1/r2 ∼ 1). The glass transition temperatures of three drug-linked homopolymers go hand in hand with the steric hindrance of three drugs, i.e., ketoprofen 〉 naproxen ≫ ibuprofen calculated the minimum energy by computer molecular modeling. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1481-1490, 1998
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 28 (1990), S. 317-321 
    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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  • 4
    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: Using VO2+ as a spin probe, a new method to obtain microenvironmental information on supports was developed which can be used in the choice of supports for coordination catalysts. Utilizing the above method, NaY was chosen as second support component. A complex support catalyst VOCl3/MgCl2/NaY/Al2Et3Cl3 was prepared and used in ethylene-propylene copolymerization. Higher polymerization activity was obtained with this catalytic system. Alternating the ratio of two kinds of supports, the composition and sequence structure of copolymers could be controlled, which showed that NaY participated in the active species, affected the insertion of monomer, and changed the composition and sequence structure of copolymers. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1439-1447 
    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: Owing to the low Tg of polystyrene, the mechanical properties of polystyrene-block-poly-butadiene-block-polystyrene (SBS) thermoplastic elastomers drop steeply above 60°C. To overcome this behavior, many research groups have considered the replacement of styrene (S) by α-methylstyrene (MS). We also attempted the synthesis of copolymers with a central polybutadiene (poly B) block and rigid blocks consisting of polystyrene (poly S) and poly(α-methylstyrene) (poly MS) blocks. Starting from a dilithium initiator, difunctional poly B's with low 1,2 content (10%) were prepared and toluene was added. After addition of a small amount of styrene, MS was added in the presence of a 15% (in vol) of THF at T ≤ -40°C. The copolymers did not have the expected structure and poor mechanical properties resulted, which were, however, still measurable at 120°C. These results probably resulted from secondary reactions involving the MS carbanions. To identify these reactions and to control the polymer structure, the synthesis of multiblock copolymers was carried out with a monofunctional polybutadienyllithium to which were added successively S and MS (in a mixture of hexane and benzene as solvent). MS was added at low temperature in the presence of small amounts of THF or at room temperature after addition of TMEDA. These attempts were unsuccessful, the copolymer being always multimodal as a result of unwanted coupling reactions involving terminal double bonds. The synthesis of elastomers using a coupling reaction of poly MS-poly S-poly B was also considered but the yield in poly B was low since termination reactions involving the polar additive occurred. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 7 (1995), S. 92-94 
    ISSN: 1040-0397
    Keywords: Glucose oxidase ; Glucose ; Carbon paste ; Methylene-green mediator ; Enzyme electrode ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An amperometric glucose bioelectrode based on the incorporation of methylene green (MG) within a glucose oxidase (GOD)-containing carbon paste is described. The electrode generates an anodic current in the range of 0.0-0.6 V (vs. SCE). The optimum pH is 8.5. The apparent Michaelis constant for the Cali bration plot is 49.3 mM (at 0.5% MG and 5.0% GOD loadings). The electrode sensitivity is 18.1 μA/mM cm2. The electrode is insensitive to paracetamol and ethanol. At 0.068 V the response to ascorbic acid (40 μM) accounts for 2.4% of that of the normal physiological glucose level in blood. The performance was optimized by systematically altering the electrode composition and electrode potential. The electrode was used to measure glucose in a serum sample and gave an acceptable correlation with the reference method Eksan-G results. Good stability was observed for storage in the dry state in the refrigerator.
    Additional Material: 5 Ill.
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  • 7
    ISSN: 1075-4261
    Keywords: cholelithiasis ; gallstone ; bile salts ; periodic precipitation ; fractal precipitation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Physics
    Notes: This is the first observation that both chaotic and periodic patterns are formed in metal ions-deoxycholate-gel systems. It is an in vitro model for approximating the conditions present during gallstone formation. The experimental results suggest that a nonlinear scientific concept such as the “butterfly effect” should be considered in understanding gallstone formation. This effect suggests that a butterfly flapping its wings in Beijing today may lead to a thunderstorm in New York months later. Applying this concept to biology, minor changes in the local chemical environment within biological systems may lead to large variations in the structure and morphology of gallstone through changes in the behavior of biological mineralization process. © 1997 John Wiley & Sons, Inc. Biospect 3: 195-205, 1997
    Additional Material: 13 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1163-1174 
    ISSN: 0887-6266
    Keywords: poly(vinyl alcohol) ; raman spectroscopy ; polymer ; aqueous solution ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We have measured the Raman spectra of ethylene-vinyl alcohol copolymer (EVOH) and poly(vinyl alcohol) (PVOH). Spectra of 88% hydrolyzed PVOH were examined from the partially crystalline solid, from PVOH dissolved in both H2O and D2O, and from films precipitated from these solutions. The spectrum in H2O differs from that of the starting material by disappearance of sharp bands having Raman shift values of 1146 and 1093 cm-1, strengthening of a band near 915 cm-1, decrease in frequency of bands at 480, 1356, and 1441 cm-1, and increase in frequency of bands at 369, 413, 1023, 1371, and 2910 cm-1. The spectrum of the film shows partial reversal of these trends. With D2O as the solvent, the band shifts are slightly different from those listed above and new bands appear. These changes are indicative of loss of crystallinity, change in stereochemistry, and partial deuteration of hydroxyl during dissolution of this PVOH sample at room temperature. © 1994 John Wiley & Sons, Inc.
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  • 9
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2018-10-12
    Description: Single-electron reduction of a carbonyl to a ketyl enables access to a polarity-reversed platform of reactivity for this cornerstone functional group. However, the synthetic utility of the ketyl radical is hindered by the strong reductants necessary for its generation, which also limit its reactivity to net reductive mechanisms. We report a strategy for net redox-neutral generation and reaction of ketyl radicals. The in situ conversion of aldehydes to α-acetoxy iodides lowers their reduction potential by more than 1 volt, allowing for milder access to the corresponding ketyl radicals and an oxidative termination event. Upon subjecting these iodides to a dimanganese decacarbonyl precatalyst and visible light irradiation, an atom transfer radical addition (ATRA) mechanism affords a broad scope of vinyl iodide products with high Z -selectivity.
    Keywords: Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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