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  • Polymer and Materials Science  (21)
  • Life and Medical Sciences  (9)
  • Wiley-Blackwell  (30)
  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The formation of a charge-transfer complex (CTC) between maleic anhydride and tetrahydrofuran both in bulk and in chloroform solution is proved by electronic absorption spectroscopy, and its association constant at 35°C is determined by this technique and by 1H NMR. The effect of irradiation with monochromatic 350 nm light upon the fluorescence spectrum of the CTC excited with this same radiation is studied. Significant changes are noted in the bulk system, but the changes are much smaller in the presence of methyl methacrylate which is simultaneously polymerized. The effect of oxygen on the polymerization is discussed.
    Additional Material: 6 Ill.
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydrosilylation reactions of 1-allyloxy-3-phenoxy-2-propanol (3) as model compound were carried out with α-dimethylsilyl-ω-hydrooligosiloxane (7; M̄n = 1200) in the presence of hexachloroplatinic acid. It was found that under stoichiometric conditions only 75--80% of the allyl groups were hydrosilylated, due to some isomerization of the allyl groups into vinyl groups, which do not undergo hydrosilylation. This isomerization could be shown to be sensitive to the type of the allyloxy structure. Thus, for example, allyloxybenzene does not undergo isomerization.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 2789-2803 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: All the side-reactions of a hydrosilylating model system (1-allyloxy-3-phenoxy-2-propanol/. . .-Si(CH3)2H in the presence of hexachloroplatinic acid (CPA); R = [CPA]/[SiH] 〉 10-4) are identified by 13C and 1H NMR. In such conditions the vinyl ether isomers and the residual silanes, formed when R 〈 10-4, are changed into several new species. The most important side-reaction consists in a silane-alcohol condensation (secondary alcohol of the model and, to a much lower extent, tertiary alcohol(tert-butyl alcohol) used as solvent of CPA), which leads to silyloxygrafted moieities. Hydrogen formed in this condensation can partially saturate the vinyl ether isomers the remaining fraction of which is cyclized into a 2-ethyl-1,3-dioxolane derivative. All the side-reactions observed in the case of the model system take place when α,β-diallyloligosulfones are polycondensated with α-dimethylsilyl-ω-hydrooligosiloxanes.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 18 (1991), S. 204-214 
    ISSN: 0886-1544
    Keywords: actin-binding ; muscle ; Z-line ; capping ; isoform ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Chicken adult muscle and liver cDNA libraries were screened with a cDNA, α1, previously isolated from a chicken embryo library by screening with antibodies against the α subunit of chicken CapZ. cDNAs with a new coding region, called α2, were found in addition to ones with the α1 coding region. α2 predicts a protein sequence that matches exactly the N-terminal sequence of 5 peptides prepared from CapZ α purified from chicken muscle, while the protein sequence predicted by α1 matches the peptides well, but not exactly. The predicted protein sequences of α1 and α2 are very similar to each other, and they are similar to those of the α subunit of capping protein from Dictyostelium [Hartmann et al., J. Biol. Chem. 163:5254-5254, 1989] and an actin-binding protein from Xenopus [Ankenbauer et al., Nature 342:822-824, 1989]. Other conserved features of the predicted primary and secondary structures are noted. Chicken α1 and α2 are transcribed in all of 7 adult chicken muscle and non-muscle tissues in comparable amounts by Northern analysis. α2 has four poly(A)+ RNA transcripts, one of which is rare in liver. α1 has two transcripts. α1 and α2 are encoded by different single-copy genes by Southern analysis of chicken genomic DNA.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 30 (1995), S. 164-170 
    ISSN: 0886-1544
    Keywords: actin ; purification ; methods ; kinetics ; Cap Z ; chickens ; antibodies ; blotting ; immuno-affinity purification ; immunoabsorbance ; muscle proteins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Gel-filtration is commonly used to remove contaminants from conventional actin prepared by the method of Spudich and Watt. It has been shown that this procedure removes the majority of a factor that reduces the low-shear viscosity of actin. We have previously reported that this factor is Cap Z, a barbed end capping protein. We now establish that, even after gel-filtration, enough Cap Z can be present in conventionally prepared actin to affect events occurring at the barbed ends of actin filaments. We also demonstrate that the concentration of Cap Z can be reduced to more than a log below the KD for binding of Cap Z to actin by either (1) immunoabsorbtion of conventionally prepared actin with anti-Cap Z antibodies, or (2) an additional cycle of polymerization/depolymerization followed by repeat gel-filtration. © 1995 Wiley-Liss, Inc.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1691-1703 
    ISSN: 0887-624X
    Keywords: 3-alkoxy-5,7-diiodo-6-fluorones ; visible photoinitiators ; acrylate photopolymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several 3-alkoxy-5, 7-diiodo-6-fluorones (λmax ≈ 470 nm) have been synthesized and evaluated as initiators for photopolymerization triggered with the 515.5 nm line of an Ar+ laser. 2-Acyl- and 2-alkyl-4,5,7-triiodo-3-hydroxy-6-fluorones were also tested at 515.5 nm. 9-Cyano-2-Acyl- and 9-cyano-2-alkyl-4,5,7-triiodo-3-hydroxy-6-fluorones were studied and could be excited with the 632 nm line of a He-Ne laser. Dyes with long linear carbon chain alkoxy groups at C-6 showed larger molar extinction coefficients and formed polymers with better mechanical properties than did compounds with shorter carbon chains, or did the corresponding C-6 phenols. The optimum side chain length of the C-6 ether alkyl group is between 4-7 carbon atoms. With longer carbon chain alkoxy groups at C-8, e.g., octyl, the mechanical properties of the formed polymers are inferior to systems formed with the butyl isomer as photoinitiator. In the case of alkoxy groups with branched alkyl groups (e.g., 2-ethylbutyl), the relationship between dye structure and the properties of the polymers formed is less straightforward. Though the dyes react from their triplet state, the fluorescence quantum yields of the dyes and the performance of the dyes as photoinitiators appear directly related. © 1995 John Wiley & Sons, Inc.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1579-1592 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Differential scanning calorimetry (DSC) has been utilized in several studies on polymerization kinetics, at different heating rates. However, there are several factors affecting the precision of kinetic parameters. In this work, the activation energy of urethane-bond formation between 2,6-tolylene diisocyanate and diethylene glycol is reported, the latter being in excess in order to minimize problems such as thermal transitions and incomplete reaction in the final step. The DSC technique was applied at different heating rates. Both the equal conversion and equal conversion rate options of the method are discussed. The latter appears to be a more adequate option for the system studied here. The results obtained show a good agreement with the model used.
    Additional Material: 8 Ill.
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  • 8
    ISSN: 0935-9648
    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
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 959-970 
    ISSN: 0887-6266
    Keywords: laser-induced processes in conducting polymer precursors ; interaction of dyes with polyelectrolytes ; lithography ; microelectronics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elimination reaction of polyelectrolyte films of poly(phenylene vinylene) precursor polymers into the fully conjugated chain was induced by irradiation with an Ar+ laser emitting at 514.5 nm. The experiments were conducted using as cast precursor polyelec-trolyte films of both the unsubstituted poly(phenylene vinylene), H-PPV, and its 2,5-dimethoxyphenylene derivative, DMEO-PPV. Precursor polymer films impregnated with an azosulfonic dye, which had a strong absorption at the laser emission wavelength, were also irradiated. The elimination reaction was followed by comparing the elemental analysis and the infrared and visibleultraviolet spectra of the irradiated and nonirradiated areas. With the unsubstituted PPV film no elimination was detected even at power fluence levels up to approximately 350 W/cm-2, but elimination and conversion to the conjugated polymer could be observed at 10 W/cm-2 when the dye was present. For DMEO-PPV the elimination reaction occurred with or without dye impregnation, and similar marking threshold values were measured in both cases. The molecular mechanism used to explain such observations and the possible application in the area of microelectronics are also discussed. © 1993 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 777-792 
    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: Binary blends of poly(vinyl alcohol) (PVA) with poly(acrylic acid) (PAA) and polyacrylamide (PAAm) were characterized by differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA), and infrared spectroscopy (IR). Molecular weight, blend composition, and heating time at 150°C were the variables used. Results obtained by DSC indicated that PAA/PVA blends are miscible in the full range of composition. Similarly, TGA traces showed that thermal stability was higher for blends than for pure polymers. Blends of PVA with high molecular weight PAA exhibited a hydrogel behavior after drying at relatively low temperature (100°C), whereas blends containing low molecular weight PAA behaved as hydrogels only after they were heated at 150°C. Hydrogel character was increased for these two PVA/PAA blends with the heating time at higher temperature (150°C). IR spectra revealed that esterification took place in these blends after thermally treated at this temperature. In contrast, addition of glyoxal in combination with heating was necessary to produce hydrogels from PAAm/PVA blends. Furthermore, the crosslinking degree of these hydrogels was estimated from their absorbency values by applying the Flory-Rehner equation. © 1993 John Wiley & Sons, Inc.
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