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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1981), S. 440-445 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of 75 analogs of trimethoprim were used in a study correlating mass spectrometric data with biological activity. Using pattern recognition techniques a correlation was obtained. Experiments to elaborate the basis of the correlation are described.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 1565-1588 
    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: An exact procedure for the objective analysis of physical data on polymers, such as volume-temperature, near known or suspected transition points, is presented. Standard computerized linear and polynomial regression techniques are employed for Y = f(X). A set of models typical of known data behavior near polymer transitions has been developed. Several sets of data for testing these models were synthesized, having a built-in random error of 0.075%. Particular emphasis is placed on the residual pattern as a function of X where a residual, RES = Y(observed-Y(calculated). RES/SE, where SE is the standard error in Y(calculated) is also employed. Residuals for the different models tested against the several sets of synthetic data provide discrimination or recognition patterns to apply when examining unknown bodies of data. We start on unknown data with the simplest possible models, a straight line and a quadratic. These yield residual patterns which guide one to more complex models, which in turn give new residual patterns. The correct model is approached objectively as a limit. We emphasize that these regression techniques can only describe the data but not interpret its physical meaning. These techniques are applied to a detailed analysis of V - T data by Wilson and Simha on poly(cylopentyl methacrylate) which show that V - T data above Tg follows two quadratics intersecting at 148-149°C. We identify this intersection as the liquid-liquid transition temperature, Tu, in basic agreement with the suggestion of Wilson and Simha.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 28 (1982), S. 525-525 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 28 (1982), S. 175-175 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 15 (1981), S. 83-96 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Analytical and experimental studies were performed to examine some characteristics of poly(methyl methacrylate) bone cement in the context of total hip replacement. Proceeding from fundamental principles of balance of energy and heat conduction, three simulation models of total hip replacement, using the finite-element method of numerical analysis, were used to predict the temperature response in the femoral prosthesis, cement, cancellous bone, and bone-cement interface. When cement collars are a centimeter or less in thickness, the models predict little likelihood of permanent bone thermal necrosis. In addition, laboratory experimental results indicate that peak temperatures attained in Simplex-P and Palacos-R cement specimens are nearly identical and that adding 0.5 and 1.0 g of the antibiotic gentamicin to Palacos-R has negligible influence on peak temperature. Experimental results also indicate that cooling cement specimens to 8°C extends the set time, which in turn could significantly increase the likelihood of stemcement loosening during surgery.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 14 (1980), S. 145-154 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: A study was conducted to measure the permeability to oxygen (PmO2) of microporous membranes coated with ultra-low-temperature isotropic (ULTI) carbon. Carbon-surfaced membranes were fabricated by application of a thin complete layer (0.7 to 1.7 microns thick) of ULTI carbon onto one surface of a microporous substrate. Based upon the average values of 27 measurements in a diffusion cell, a mean reduction in PmO2 of only 10% results following the treatment of the microporous substrate with ULTI carbon. The values for PmO2 are not dependent upon the thickness of the carbon film over the range of film thickness of 0.7 to 1.7 microns. When coupled with the known antithrombotic characteristics of ULTI carbon, an oxygenator incorporating carbon-surfaced microporous membranes has the potential for use in clinical extracorporeal membrane oxygenation (ECMO).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 15N Chemical shifts of cis-decahydroquinoline, N-methyl-cis-decahydroquinoline, and of 19 methyl substituted NH- and NCH3-cis-decahydroquinolines are reported. Shift values of conformationally homogeneous compounds can be used to determine the chemical shifts of the possible conformations of the mobile compounds. Equilibrium constants derived from the shifts of the contributing conformations agree with results of low temperature 13C NMR spectroscopy.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of para- and meta-substituted acetophenones were prepared which were highly labeled with 18O at the carbonyl function. The natural abundance 13C NMR spectra of the compounds were recorded and the 18O-isotope-induced shifts of the carbonyl carbon were measured in order to determine possible substituent group electronic effects on the 18O-isotope shift. The isotope shifts were found to be correlated with a number of properties which demonstrate the molecular basis of the isotope shift. Good correlations were obtained for the isotope shift as a function of σp+, the carbonyl stretching frequency, the carbonyl group bond order, the n→π**transition of the carbonyl group and the chemical shift of the ipso carbon. In contrast, no correlation was observed between the magnitude of the 18O-induced isotope shift and the 13C chemical shift of the carbonyl carbon. These properties are discussed in connection with the theoretical basis of the isotope shift.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 20 (1981), S. 141-154 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pKa of 3,8-diamino-6-phenyl-phenanthridine (DAPP), a nonquaternary analog of ethidium bromide, has been determined spectrophotometrically as a function of sodium ion concentration both free in solution and complexed to DNA. Unwinding angle determinations with this compound were determined with Col El DNA using ethidium bromide as a standard. The unwinding angle for DAPP was 24 ± 2° relative to 26° for ethidium, and this suggests that DAPP binds in a manner quite similar to ethidium and with no significant outside bound DAPP under these experimental conditions. Isobestic behavior was obtained on spectrophotometric pH titration above pH 5 as long as the ratio of DNA-phosphate to ligand was between 100 and 300 and the DNA phosphate concentration was approximately 0.01M or greater. The loss of isosbestic behavior which occurred below pH 5 is probably due to titration of the 8 amino group of the ligand complexed to DNA. To circumvent this problem, pKa values and the extinction coefficient of the acidic species were both determined by a computer program using experimental data obtained above pH 5. The pKa of the free compound has only a minor dependence on ionic strength, while the pKa of the ligand bound to DNA in an intercalated complex depends strongly on the sodium ion concentration. The pKa of the DAPP-DNA complex is a linear function of -log[Na+] as predicted by the ion-condensation theory of polyelectrolytes. It was determined that DAPP is essentially completely bound to DNA under the conditions of these experiments by (1) determination of apparent pKa values as a function of total DNA concentration, (2) calculation of binding constants for the neutral species of DAPP, and (3) spectral analysis of the protonated and neutral species of DAPP bound to DNA relative to DAPP free in solution. These results support the ion-condensation theory; provide an independent method for measuring ψ*, the average number of counterions associated per phosphate of DNA in the intercalated conformation; and illustrate that there are no specific pH effects or absolute pKa values for ligands bound to DNA, but only ionic-strength-dependent results.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 1621-1632 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several intercalating dyes are shown to inhibit the cation-induced condensation of λ-DNA when Co3+(NH3)6 is the condensing agent. The dyes that have been studied are ethidium, propidium, proflavin, quinacrine, and actinomycin D. Earlier work has shown that intercalating dyes inhibit ψ-DNA condensation. [Lerman, L. S. (1971) Prog. Mol. Subcell. Biol. 2, 382-391; Cheng, S. & Mohr, S. C. (1975) Biopolymers 14, 663-674.] Dye-induced decondensation of intramolecularly condensed DNA has been studied by making use of conditions in which Co3+(NH3)6 produces intramolecular condensation without significant aggregation. Some aggregation is caused, however, during dye-induced decondensation. Dye titration curves of DNA decondensation have been measured by excess light scattering to monitor decondensation and by fluorescence to monitor intercalation. All of the dyes studied act as competing cations in displacing the condensing cation Co3+(NH3)6 from the DNA. Competition occurs both in and below the transition zone for condensation. The effectiveness of a dye as a competing cation increases with its net positive charge. Before decondensation begins, no intercalated dye can be detected, suggesting that intercalation might be incompatible with the proper helix packing needed for cation-induced DNA condensation. To test this last point, methidium-spermine was synthesized: it contains an intercalating methidium head group combined with a polyamine tail. Methidium-spermine is found to cause λ-DNA condensation, but aggregation accompanies condensation, as has been found earlier for spermine and spermidine. Fluorescence and absorption spectra indicate that the methidium group is intercalated when the DNA is condensed, indicating that intercalation need not be incompatible with DNA condensation. The presence of aggregates among the condensed DNA molecules makes this last conclusion tentative.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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