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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 104 (1982), S. 4492-4494 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 47 (1982), S. 4786-4789 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0827
    Keywords: Cancellous bone ; Bone strength ; Osteoporosis ; Trabecular bone quality
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary This paper discusses two novel applications of nuclear magnetic resonance (NMR) as an investigational tool for the assessment of cancellous bone microarchitecture. It further outlines extensions of the method forin vivo clinical evaluation of bone strength in patients with skeletal disorders such as osteoporosis. The first method relies on the hypothesis that the presence of two phases of different magnetic permeability, i.e., bone and bone marrow, causes a spatial nonuniformity of the magnetic field across the measurement volume. The resulting spread in resonance frequency shortens the decay time constant (T2*) of the time domain proton signal in bone marrow or its substitute (water). Increased trabecular spacing, such as it occurs in osteoporosis, reduces the spatial field inhomogeneity and thus prolongs T2*, which has been shown bothin vitro andin vivo. Subjects with osteoporosis, characterized by either low bone mineral density and/or spine compression fractures, have T2* values that are significantly prolonged. The second method focuses on a direct measurement of micromorphometric parameters of cancellous bone, using the principles of proton NMR microscopy in conjunction with computer processing of the resulting digital images. Image contrast between the trabeculae and the intertrabecular space is based on the marrow protons providing a signal, as opposed to bone, which appears with background intensity. Once tissues have been classified (into bone and marrow), for example, by means of a histogram-based segmentation algorithm, bone area fraction, mean trabecular plate density (MTPD), and mean trabecular plate thickness (MTPT) can be computed without the need for further operator intervention. The most critical parameter for successful implementation is image slice thickness which determines the extent of partial volume blurring. At 400 MHz spectrometer frequency (9.4 T field strength), images of appropriate resolution can be obtained from a 1 cm3 specimen of vertebral cancellous bone in 1 hour or less. It is shown that for relatively isotropic cancellous bone such as the one found in the vertebrae, a slice thickness on the order of 200 μm is adequate, with an inplane resolution on the order of 50 × 50 μm2 As an illustration of the technique, the relationship among the different stereologic parameters in cadaver specimens of human lumbar vertebrae is reported, showing a strong association between the area fraction and both MTPD and MTPT. The chief benefit of the new technique is its nondestructive nature and its ability to provide histomorphometric images from multiple physical locations and in multiple planes, which is desirable because of the large spatial variations in the morphologic parameters within the bone. Finally, the technique is demonstrated to be potentially also noninvasive, as illustrated with images from the human finger, acquired on a modified 1.5 Tesla clinical magnetic resonance imaging system at a pixel size of 95 × 95 μm2
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unambiguous signal assignments in the 13C spectra of monodeuterated cyclooctanones derived from the lead tetraacetate or silver oxide/bromine oxidations of the corresponding 1-monodeutero-alcohols have been obtained from deuterium-induced 13C isotope shifts and geminal and vicinal 13C—2H spin-spin coupling constants. The label in the ketones is shown to be in position 5.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C shifts of the alkaloids roxburghine B, C, D and E are determined. They confirm the following configurations for the last three bases: C(18α)-normal, C(18α)-pseudo and C(18β)-pseudo, respectively. Roxburghine B is shown to be a C(18β)-epi-allo isomer.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 176 (1975), S. 1071-1119 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Wahrscheinlichkeiten der kompositiv-konfigurativen Triaden in taktischen und ataktischen Methylmethacrylat/Methacrylsäure-Copolymeren werden ermittelt. Nach Sicherung der Zuordnung von syndiotaktischen und isotaktischen Triaden in den 1H-NMR Spektren der taktischen Copolymeren in drei NMR-Lösungsmitteln werden die chemischen Verschiebungen der heterotaktischen Triaden mit Hilfe von Verschiebungsinkrementen postuliert. Die postulierte Zuordnung der heterotaktischen Triaden wird gestützt durch den Vergleich der experimentell gefundenen 1H-NMR Peak-Intensitäten von ataktischen Methylmethacrylat/Pentadeuteromethacrylsäure-Copolymeren und Pentadeuteromethylmethacrylat/Methacrylsäure-Copolymeren in drei Lösungsmitteln mit den berechneten Triadenwahrscheinlichkeiten. Die zur Berechnung der Triadenwahr-scheinlichkeiten notwendigen kompositiven und konfigurativen Größen werden ermittelt. Es wird gezeigt. wie die Peak-Flächen in den Spektren der partiell deuterierten Copolymeren in verschiedenen Lösungsmitteln miteinander kombiniert werden können, urn die Wahrscheinlich keiten der kompositiv-konfigurativen Triaderi in ataktischen Copolymeren zu ermitteln. Möglichkeiten ziir Auswertung von Triadenwahrscheinlichkeiten aus den 13C-NMR Spektren von taktischen und ataktischen Methylmethacrylat/Methacrylsäure Copolymeren werden aufgezeigt.
    Notes: The probabilities of compositional-configurational triads in tactic and atactic methyl methacrylate/methacrylic acid copolymers are evaluated. After verification of the assignment of syndiotactic and isotactic triads in the 1H-NMR spectra of tactic methyl methacrylate/methacrylic acid copolymers in three NMR solvents, the chemical shifts of the heterotactic triads are postulated by shift increments. The postulated assignment of the heterotactic triads is supported by comparison of the experimental 1H-NMR peak intensities of atactic methyl methacrylate/pentadeuteromethacrylic acid copolymers and atactic pentadeuteromethyl methacrylate/methacrylic acid copolymers in three NMR solvents with calculated triad probabilities. The compositional and configurational parameters needed for the calculation of triad probabilities are determined. It is shown how the peak areas obtained from the two partially deuterated, atactic copolymers in different solvents may be combined to determine the probabilities of all compositional-configurational triads in atactic copolymers. Possibilities for the evaluation of triad probabilities from the 13C-NMR spectra of tactic and atactic methyl methacrylate/methacrylic acid copolymers are presented.
    Additional Material: 24 Ill.
    Type of Medium: Electronic Resource
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