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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 41 (1985), S. 342-346 
    ISSN: 1420-9071
    Keywords: Chemiluminescence ; anesthesia ; surgery ; abdominal ; granulocytes ; perioperative period ; immunological resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The effect of anesthesia and major abdominal surgery on zymosan-induced chemiluminescence (CL) of neutrophil granulocytes was evaluated. CL was measured in diluted whole blood taken at distinct intervals within the perioperative period. In addition, blood samples from healthy volunteers were supplemented with ether and halothane to investigate the in vitro effect of these agents. The phagocytosis-induced CL was not found to be depressed by anesthesia and surgery. Only at supranarcotic concentrations was CL reduced. Surgery and anesthesia, therefore, do not appear to impair this defense system significantly under the conditions of this investigation.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 385-400 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrochemical Reduction of 4-Substituted 7-Nitro-benzo-furazansThe electrochemical properties of 4-methoxy-, hydroxy-, alkylamino, and arylaminosubstituted 7-nitrobenzofurazans (1a-1h) are studied between pH 1,7 and 11,6 by use of buffer solutions containing different portions of various organic solvents. Reduction waves which are present in polarograms, are well reproducible and practicable for qualitative and quantitative analysis of amines. A mechanism of reduction is suggested by reason of polarographic and coulometric results. The half wave potentials are correlated with various substituent constants. A value of ϱ = + 0,32 follows from the determination of the reaction constant from the slope of the E 1/2 - σp - relation for the polarographic reduction of each nitro-function.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 487-504 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Derivatization of Amines with 4-Substitured 7-NitrobenzofurazansElectrophilc derivatives of 4-nitro-benzofurazan with different reactivities were used to synthesize 28 new mono- and disubstituted 4-amino-7-nitrobenzofurazans 2b, 2d, 2f-2i, 2l, 2m-2n, 3b-3f, 3h-3j, 4e-4d, 4f-4k, 4m, 4o-4p. A reaction mechanism is proposed on the basis of the differences of the reactivities and a preliminary kinetic examination. The acid character of the N—H-function in monosubstituted compounds is demonstrated by means of spectroscopical investigation of pKa-values.Data from i.r., u. v./vis, and fluorescence studies are offered.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 261-274 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: UV-VIS- and IR-Spectroscopic Studies with N-Substituted 4-Amino-7-nitro-benzofurazansStarting from spectra of parent substance benzofurazan the influence of different functional groups (NO2, OH, NH2, NHAlk, NAlk2, NHAr, NArAlk) in 4- and (or) 7-position on the shape of spectra and the intensity of individual bands was examinated. It was tried to assign spectral bands to defined absorptions in the u.v./vis and i.r. range. The long-wave band in the solution-VIS-spectra of N-substituted 4-amino-7-nitrobenzofurazans was identified as a charge-transfer band. By the use of constants α, β, and π* by Kamlet and Taft the influence of different properties of solvents was correlated with band shifts in the UV/VIS range. A qualitative correlation was found between \documentclass{article}\pagestyle{empty}\begin{document}$ \bar \nu _{{\rm max}} $\end{document} of the long-wave band in the VIS-spectra, the polarographic half wave potential E 1/2 and the sum of polar substituent constants Σσ* of Taft. These proportions were plotted in a three-dimensional diagram.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 745-754 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Intramolecular Quinhydrones. II. Synthesis and Oxidation Characteristics of Unsymmetrically Bridged DihydroquinonesBy ether cleavage with AlCl3 or AlBr3 the synthesized unsymmetrically bridged tetramethoxy derivatives 2a-w were converted into the corresponding tetravalent hydroquinones 3a-r and these were oxidized to the yellow diquinones 4a-p or partially to the deeply coloured intramolecular quinhydrones 6a-o.
    Notes: Die synthetisierten unsymmetrisch verbrückten Tetramethoxyderivate 2a-w wurden durch Ätherspaltung mit AICl3 oder AlBr3 in die entsprechenden tetravalenten Hydrochinone 3a-r übergeführt und diese zu den gelben Dichinonen 4a-P oder partiell zu den tieffarbigen intramolekularen Chinhydronen 6a-o oxidiert.
    Additional Material: 5 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 1015-1020 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Intramolecular Quinhydrones. III. Colour and Charge-transfer InteractionsThe intensive colour of the crystalline intramolecular quinhydrones 2a-o depends on the substitution and the unsymmetrical bridge-structure. The solutions are yellow coloured. According to the x-ray, i.r.- and u.v./vis-results there are for 2a-o inter, but no intramolecular CT-complexes.
    Notes: Die intensive Farbe der kristallinen intramolekularen Chinhydrone 2a-o hängt von der Kernsubstition und der unsymmetrischen Brückenstruktur ab. Lösungen sind nur gelb gefärbt. Nach den Ergebnissen röntgenkristallographischer, IR- und UV/VIS-spektroskopischer Untersuchungen bilden 2a-o inter-, aber keine intramolekularen CT-Komplexe.
    Additional Material: 2 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 318 (1976), S. 635-642 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Electrochemical Behaviour of Asymmetrically Bridged DiquinonesRedox potentials and pK-values of tetravalent asymmetrically bridged diquinones, quinhydrones, and hydroquinones are described and the influences of substituents on these characteristics are discussed.
    Notes: Es werden Redoxpotentiale und pK-Werte von tetravalenten, unsymmetrisch verbrückten Dichinonen, Chinhydronen und Hydrochinonen beschrieben und Substituenten-einflüsse auf diese Eigenschaften diskutiert.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1877-1894 
    ISSN: 0887-6266
    Keywords: liquid crystals ; crystallization metastable phases ; rates of phase transformation ; morphology ; competition between phases ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization of the monotropic liquid crystal forming polyether, poly-n-nonyl-4 4′-biphenyl-2-chloroethane, was investigated using DSC calorimetry and polarizing optical microscopy. The principal theme was the nature of crystallization from the nematic liquid crystalline state, which in the monotropic system could be directly compared with the more familiar crystallization from the isotropic melt using one and the same compound. Novel, polarizing optical structures were observed that combine features of both the usual LCPs (fine “grains”) and those of the conventional crystallizeable polymers (spherulites) with differing degrees of prominence of each according to crystallization conditions. The considerations of such structural observations, combined with the calorimetric results and the newly gained information on the kinetics of the crystallization process, reveal an acceleration of the overall crystallization rate at the stage where liquid crystal formation sets in as assessed by calorimetry but not as registered with the polarizing microscope, leading to wider issues regarding the conception of “amorphous crystalline ratio” and its extension to the liquid crystal state. Beyond polymers, the new findings lead to the more general considerations on metastable phases, specifically to their emergence and competition with the phases of ultimate stability. In this respect the present study on a monotropic LCP provides an illustrative example of a more general treatment presented previously. © 1995 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 28 (1990), S. 655-674 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Quantitative thermal analysis of a family of semicrystalline polyimides containing from one to three ethylene glycol spacer units has been conducted. Special emphasis has been placed upon the changes in the thermodynamic properties resulting from the successive additions of ethylene glycol units. The solid and liquid heat capacities were measured in the temperature range 230-640 K. The solid heat capacities were also calculated from the vibration spectra of the polymers. An in-depth description of the glass transitions, the heat capacity increases at the glass transition temperatures, and the widths of the glass transitions is provided. Three parts of the heat of fusion have been identified: Wc (H), that contributed from the high melting peak; wc (L), that contributed from the low melting peak; and wc (C), that developed during cooling after isothermal crystallization. The metastability, sequence of crystallization, and rate of reorganization of the low and high melting peaks have been investigated by stepwise crystallization and by analysis using different heating rates after isothermal crystallization. A rigid amorphous fraction is needed to explain the failure of the two-phase (crystallinity) model.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 299-310 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Differential scanning calorimetry (DSC) and in situ small-angle x-ray scattering (SAXS) indicate that in an α ω-methoxy-poly(ethylene oxide) (MPEO) fraction (MW 3000) a transient nonintegral folding (NIF) crystal initially forms during crystallization throughout a wide range of crystallization temperatures. Subsequent transformations of the NIF to IF (integral folding) crystals at low temperatures occur mainly through isothermal thickening or thinning via perfection processes or, at higher temperatures, through primary crystal formation. The NIF crystal is thermodynamically the least stable state among the crystal forms, but its growth is the most rapid. The overall crystallization and crystal melting of this MPEO fraction reveal that the NIF crystal and the NIF → IF crystal transformations are common to low-molecular mass PEO fractions without regard to the end group. Nevertheless, diffusion coefficient and viscosity measurements provide clear evidence of an end-group effect in PEO and MPEO fractions. The difference in the overall crystallization and isothermal thickening and thinning kinetics of low-molecular mass PEO and MPEO fractions can lead to further understanding of end-group effects.
    Additional Material: 11 Ill.
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