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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 345 (1973), S. 179-193 
    ISSN: 1432-2013
    Keywords: Aplysia ; Pacemaker Neuron ; Glycolysis ; ATP Hydrolysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Completely isolatedAplysia pacemaker neurons were used to investigate mechanisms of endogenous electrical rhythmicity. This preparation allows the study of pure pacemaker activity free from synaptic, ephaptic and/or humoral influences from the surrounding cells. The effect of some substances quite different in their mode of biochemical action were tested: sodium iodoacetate, phloridzin, dinitrophenol, heavy water, and ouabain. Each of these substances suppressed the spontaneous spike activity without any marked depolarizing or hyperpolarizing effect. Spontaneous spike activity of the neurons silenced after addition of one of these substances reappeared after addition of glucose. The restoring effect of glucose failed in beating pacemaker neurons silenced by ouabain, but is present in ouabain silenced pacemaker cells of the oscillatory type. It is suggested that two basic biochemical processes: glycolysis and ATP hydrolysis are involved in the rhythmogenesis. The results offer some hints that the spike rhythms of pacemaker neurons depend on a certain balance between glycolytic processes and ATP hydrolysis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 75-85 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new route to prepare optically active polyamides was established, based on the polycondensation of two new active diesters: the active diesters of 4-chloro-1 hydroxybenzotriazole, such as 1,1'-(terephthaloyldioxy)bis(4-chloro-benzotriazole), and 1,1'-(isophthaloyldioxy)bis(4-chlorobenzotriazole), with optically active isomers of 2,4-diaminopentane. Dipolar aprotic solvents such as N,N-dimethylformamide and dimethyl sulfoxide were used as reaction solvents. The solution polycondensation carried out in solution at room temperature afforded optically active polyamides. The aminolysis of the two active diesters was carried out as a model reaction study.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 167-171 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 127-136 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radicals formed in poly(methyl methacrylate) (PMMA) under vacuum by UV irradiation at room temperature were carefully examined from 77 K to 300 K by electron spin resonance (ESR). The conventional nine-line spectrum was observed with significant overall intensity changes in contrast to previous reports. The intensity decreases greatly as the temperature increases from 77 K to 100 K. The intensity of the ESR spectrum increases as the temperature increases gradually from 100 K to 260 K. The spectral changes were reversible at all temperatures. Three different models are considered to interpret the temperature dependence of the intensity of the ESR spectrum. The results indicate that the ESR spectrum depends on (1) the steady-state concentration of the propagating radical in the polymer, (2) the conformational distributions of the radicals, and (3) the environmental structures of the polymer matrix.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1539-1547 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photochemical polymerization rates of isoprene, ethyl methacrylate, and of styrene in various aromatic solvents were measured. The average lifetimes of propagating radicals were measured by the rotating sector method. The polymerization rate constants, Kp, were determined and compared with dipole moments (μ) and Hammett σ constants for the aromatic solvents. Linear correlations of log(kp/kp, benzene) vs. μ and σ were obtained.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 389-403 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polynucleotide analogs consisting of poly(vinylamine) as the backbone and optically active thymine and adenine derivatives as the pendants were synthesized. The pendants were prepared by the addition reaction of the nucleic acid base to ethyl crotonate followed by hydrolysis. The pendants were resolved using brucine as the resolving agent and an acetone-water mixture as the fractional crystallization solvent. The active esters of the pendants also were prepared. Poly(vinylamine) was isolated from water employing a weak acid, N-hydroxysuccinimide (HOSu), to protect the amino group of the poly(vinylamine). Model reactions for grafting were examined. Grafting reactions were carried out by reacting the active esters with the PVAm.6HOSu complex at room temperature.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 373-388 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polynucleotide analogs with a polyethylenimine backbone and optically active thymine- and adenine-containing pendants and their model compounds were synthesized. The pendants were prepared by the addition reaction of the nucleic acid base to ethyl crotonate. The ammonium salt of 3-(adenin-9-yl)butyric acid was employed to replace its free acid for the formation of diastereomeric salt with brucine. Fractional crystallization of the diastereomeric salt generates the partially resolved enantiomers. The solubility difference between the racemic mixture and its enantiomer was utilized to obtain the pure enantiomers. The active esters of the pendants were prepared. Grafting reactions were carried out by the reaction of active esters with PEI at room temperature. Completely grafted polymers were obtained.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 24 (1986), S. 627-630 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 265-272 
    ISSN: 1042-7147
    Keywords: polyurethane ; bismaleimide ; biomaterial ; blood compatibility ; surface property ; mechanical property ; degree of compatibility ; 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
    Notes: Interpenetrating polymer networks (IPNs) of polyurethane (PU) and maleimide-terminated polyurethane (UBMI) were prepared by using a simultaneous polymerization technique. The effects of the UBMI molecular weight and amounts of the UBMI in the IPNs on the mechanical properties, dynamic mechanical properties, degree of compatibility, water absorption, surface properties and dynamic thrombosis were investigated. Bulk structure and surface properties were analyzed in order to correlate their blood compatibility. The IPNs exhibited a higher ultimate tensile strength especially when the UBMI with short soft chains was introduced. The heterogeneous characteristics were found for the IPNs when longer soft segment chains were incorporated in the PU component polymer. The presence of hydrophilic/hydrophobic alternative microdomains on the IPN surface was proposed to be the reason for good blood compatibility. The degree of compatibility, compositions of each domain and content of each domain in the matrix were calculated and correlated with the blood compatibility.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 1573-1588 
    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: A unique series of ethylene and propylene sequential polymerization experiments have been carried out in a stirred bed gas phase reactor using unsupported Stauffer AA catalyst (TiCl3· \documentclass{article}\pagestyle{empty}\begin{document}$\frac{1}{3}$\end{document}AlCl3). Several interesting kinetic results were observed. It was found that propylene causes rate enhancement for a subsequent ethylene polymerization but that ethylene causes a rate reduction for a subsequent propylene polymerization. Furthermore, the rate enhancement/reduction effect increases with the duration of the preceding polymerization. Chemical/kinetic effects were found to be the likely causes of both the rate enhancements and the rate reductions observed during sequential polymerization. It was also shown that enhanced monomer sorption caused by the presence of a more soluble component, such as a heavier comonomer, does contribute to rate enhancement during simultaneous copolymerizations, but is not a factor for sequential polymerizations. © 1993 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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