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  • AIRCRAFT  (53)
  • Analytical Chemistry and Spectroscopy  (46)
  • 1975-1979
  • 1970-1974  (99)
  • 1972  (99)
Collection
Keywords
Publisher
Years
  • 1975-1979
  • 1970-1974  (99)
Year
  • 1
    Electronic Resource
    Electronic Resource
    13C, 14N, 15N and 17O NMR spectra of nitropyrroles and nitroimidazoles (1972)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 153-160 
    Details
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon, nitrogen and oxygen NMR spectra of some nitro derivatives of pyrrole and imidazole have been investigated. The 13C chemical shifts of para-carbons and the 17O chemical shifts of the nitro group correlate qualitatively with the electron densities on these carbon and oxygen atoms, which in turn depend upon the degree of conjugation of the nitro groups with the heterocyclic ring. Conjugation of several nitro groups with the benzene ring is in most cases not impaired by mutual interactions and the 13C shifts show good additivity. Such additivity is much worse in pyrrole and imidazole derivatives. Taken together with the diamagnetic nature of these deviations from additivity, this leads to a possible conclusion about the less pronounced conjugation of the nitro groups with the heterocyclic ring in heterocyclic dinitro derivatives.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1270040118
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    13C, 14N, 15N and 17O NMR spectra of the charged species of nitropyrroles and nitroimidazoles (1972)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 197-202 
    Details
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Changes in 13C and 14N chemical shifts of the nitro derivatives of nitrogen heterocycles upon ionization (anion or cation formation) are twofold - first a uniform paramagnetic or in the case of protonation, a uniform diamagnetic shift of all the ring resonances that parallels the changes in the respective ultraviolet spectra and must be caused by changes in the molecular excited states, and second - the influence of the conjugated nitro group. About one third of the total negative anion charge may be localized on the nitro group, which causes unusually large shifts of the ring 13C resonances in this case.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1270040202
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  • 3
    Electronic Resource
    Electronic Resource
    An NMR study of phenol self-association (1972)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 453-462 
    Details
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper presents a study of the chemical shift of the phenol hydroxyl group as a function of concentration and temperature in cyclohexane, methylcyclohexane and carbon tetrachloride solutions. The chemical shift of monomeric phenol has been found. For these solutions monomertrimer equilibrium is observed within the entire temperature range and within a wide concentration range. At low phenol concentrations, from 1 to 3 mole-%, the monomer-dimer equilibrium is observed in cyclohexane, methylcyclohexane and carbon tetrachloride solutions. Chemical shift of the hydroxyl group of trimeric phenol is temperature-dependent.From the experimental data the association constants and thermodynamic functions of the systems under study have been determined. The association constants differ for the above systems at the same temperatures. Association entropy ΔS changes from one system to another, while ΔH is the same for all systems.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1270040404
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  • 4
    Electronic Resource
    Electronic Resource
    Mass spectra of methylsubstituted monosila- and monogermacyclobutanes, 1,2- disila- and 1,2-digermacyclopentanes. Some correlations with thermal decomposition (1972)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 309-316 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of 1,1-dimethyl-1-silacyclobutane (I - as reported by Cherniak et al.),6, 1,1-dimethyl-1-germacyclobutane (II), 1,1,2,2-tetramethyl-1,2-disilacyclopentane (III) and 1,1,2,2-tetramethyl-1,2-digermacyclopentane (IV) are compared and some correlations between electron-impact fragmentation and thermal decomposition are derived. The mass spectra of the germanium compounds with respect to the silicone compounds are enriched by light fragment ions and exhibit lower intensities of odd-electron ions. The composition of some ions and apparently of neutral fragments coincides with that of the unstable intermediates which are suggested in the thermal decomposition mechanism of some related compounds. The loss of C2H4 is more characteristic under electron-impact as well as in thermal decomposition of Si-compounds, while C3H6 is preferable eliminated by the Ge-compounds.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210060309
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  • 5
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    Fixed base simulator study of an externally blown flap STOL transport airplane during approach and landing (1972)
    In:  CASI
    Details
    Publication Date: 2019-06-27
    Description: A fixed-base simulator study was conducted to determine the flight characteristics of a representative STOL transport having a high wing and equipped with an external-flow jet flap in combination with four high-bypass-ratio fan-jet engines during the approach and landing. Real-time digital simulation techniques were used. The computer was programed with equations of motion for six degrees of freedom and the aerodynamic inputs were based on measured wind-tunnel data. A visual display of a STOL airport was provided for simulation of the flare and touchdown characteristics. The primary piloting task was an instrument approach to a breakout at a 200-ft ceiling with a visual landing.
    Keywords: AIRCRAFT
    Type: NASA-TN-D-6898 , L-8394
    Format: application/pdf
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    NASA TECHNICAL REPORTS
  • 6
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    Techniques in balloon X-ray astronomy. (1972)
    In:  Other Sources
    Details
    Publication Date: 2019-06-27
    Description: Since the first balloon observation of the Crab Nebula balloon data have provided much information on the positions, spectra, time variability and pulsed nature of localized sources, and on the spectrum and isotropy of diffuse galactic and universal components. Measurements are limited to energies above about 20 keV by atmospheric attenuation at 2 to 3 g/sq cm depth and to below several hundred keV by detector sensitivity. Detectors usually consist of large-area Na I or Cs I scintillation counters with anticoincidence collimators for rejection of charged particles and scattered X-rays. Proportional counters are occasionally used at lower energies and solid-state detectors are used where extreme energy resolution is important. The instruments require a pointing capability on the order of 1.0 to 0.1 deg, depending on the collimator aperture. Digital data is either recorded on board or telemetered using a PCM technique.
    Keywords: AIRCRAFT
    Type: Space Science Reviews; 13; June 197
    Format: text
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    NASA TECHNICAL REPORTS
  • 7
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    Study of Load Alleviation and Mode Suppression (LAMS) on the YF-12A airplane (1972)
    In:  CASI
    Details
    Publication Date: 2019-06-27
    Description: The potentials and capability for implementing a LAMS (load alleviation and mode suppression) system on the YF-12A for the purpose of flight research were evaluated. The nature of the research is to minimize the design risk in application of LAMS to future aircraft. The results of the study show that the YF-12A would be a suitable test bed for continuing development of LAMS technology. This was demonstrated by defining five candidate LAMS systems and analytically evaluating them with regard to performance and mechanization. Each of the five systems used a different combination of force producers. A small canard vane or a mass-reaction device mounted near the cockpit was considered as a possible LAMS force producer, together with the existing inboard and outboard elevons. It was concluded that a combination of canard vane and outboard elevons would provide the most effective system for the YF-12A.
    Keywords: AIRCRAFT
    Type: NASA-CR-2158
    Format: application/pdf
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    NASA TECHNICAL REPORTS
  • 8
    Electronic Resource
    Electronic Resource
    Mass spectrometry in the investigation of β-lysine-containing peptides (1972)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 1-8 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectrometry can be used for amino acid sequence determination in β-lysine-containing peptides and for the identification of α- and β-lysine residues in peptides, as well as for amide bond type determination in β-lysine peptides. The peptide bond in streptothricin D is shown to be formed through the participation of an ε-amino group of the L-β-lysine residue.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210060102
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  • 9
    Electronic Resource
    Electronic Resource
    Ionization and dissociation of some perfluoroalkylene-linked silanes and cyclic siloxanes under electron-impact (1972)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 425-427 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of two silanes and two cyclic siloxanes of the general formulae HSi(CH3)2-C6H4—(CF2)n—C6H4(CH3)2SiH and (n = 2 and 3) are reported and discussed. Although some major differences are apparent between the spectra of the two silanes, the fragmentation patterns of the cyclic siloxanes are largely identical.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210060408
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  • 10
    Electronic Resource
    Electronic Resource
    The mass spectra of carboxylic acids - V: Carboxyl-carboxyl interaction in the fragmentation of some cycloalkene-1,2-dicarboxylic acids (1972)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 6 (1972), S. 549-557 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The fragmentation mechanisms of the six isomeric cyclohexene-1,2-dicarboxylic acids are discussed. Only the 1-cyclohexene acid, by virtue of the major sequential losses of H2O and CO2 from the molecular ion, is readily distinguishable from its isomers, all of whose mass spectra are closely similar. In contrast to cis and trans cyclohexane-1,2-dicarboxylic acids, whose mass spectra were markedly different, the cis and trans cyclohexene-1,2-dicarboxylic acids fragment in a similar fashion. The mass spectra of 1-cyclopentene-1,2-dicarboxylic acid and 1-cyclobutene-1,2-dicarboxylic acid also exhibit a strong carboxyl-carboxyl interaction; the fragmentation behaviour of the 1-cyclopenteneacid is, however, more complex than that of the 1-cyclohexene and 1-cyclobutene acids.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210060511
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