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  • Organic Chemistry  (11)
  • SPACE SCIENCES  (6)
  • 15A63  (1)
  • Trichogrammatidae
  • 1985-1989  (3)
  • 1970-1974  (15)
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  • 1
    Publication Date: 2019-06-27
    Description: Luminescence of Apollo 11 and 12 rocks measured with UV, X ray, and proton radiation
    Keywords: SPACE SCIENCES
    Type: NASA-CR-114970
    Format: application/pdf
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  • 2
    Publication Date: 2019-06-27
    Description: Luminescence measurements on Apollo 11 and Apollo 12 lunar soil samples
    Keywords: SPACE SCIENCES
    Type: NASA-CR-114899
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  • 3
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    In:  Other Sources
    Publication Date: 2019-07-13
    Description: Luminescence efficiencies of Apollo 11 lunar and terrestrial rocks and minerals, using UV excitation
    Keywords: SPACE SCIENCES
    Type: APOLLO 11 LUNAR SCIENCE CONFERENCE; Jan 05, 1970 - Jan 08, 1970; HOUSTON, TX
    Format: text
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  • 4
    Publication Date: 2019-07-13
    Description: Luminescence measurements were made of Apollo 14 lunar samples with far UV X-ray, and proton irradiation and of Apollo 15 lunar samples with X-ray irradiation. Preliminary efficiencies with the far UV are in the range 0.001 to 0.01; efficiencies with X-rays and protons are in the range 10 to the -8th to 10 to the -6th powers. The crystalline igneous rocks show higher efficiencies, in general, than the breccias and glasses, and the ratio of intensity of the green to the blue luminescence peak tends to be higher for the crystalline igneous rocks than for breccias and glasses. Therefore, both the efficiency and the spectral character appear to have a systematic relationship to lithologic type (granitic versus gabbroic versus fragmental) and to geologic history and processes on the moon (shocked versus unshocked or only mildly shocked material).
    Keywords: SPACE SCIENCES
    Type: NASA-CR-115512
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  • 5
    Publication Date: 2019-07-13
    Description: Luminescence measurements have been made of Apollo 14 lunar samples with far UV, X-ray, and proton irradiation and of Apollo 15 lunar samples with X-ray irradiation. Preliminary efficiencies with the far UV are in the range .01 to .001; efficiencies with X-rays and protons are in the range .000001 to .00000001. The crystalline igneous rocks show higher efficiencies, in general, than the breccias and glasses, and the ratio of intensity of the green to the blue luminescence peak tends to be higher for the crystalline igneous rocks than for the breccias and glasses.
    Keywords: SPACE SCIENCES
    Type: Lunar Science Conference; Jan 10, 1972 - Jan 13, 1972; Houston, TX
    Format: text
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  • 6
    Publication Date: 2019-07-13
    Description: Apollo 11 and 12 rocks luminescence under proton, electron, UV and X irradiation
    Keywords: SPACE SCIENCES
    Type: LUNAR SCIENCE CONFERENCE; Jan 11, 1971 - Jan 14, 1971; HOUSTON, TX
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Order 4 (1987), S. 233-256 
    ISSN: 1572-9273
    Keywords: 06A15 ; 06C05 ; 06C99 ; 11E04 ; 11E99 ; 15A63 ; Orthogonal geometry ; computation of lattices
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract Hermitean vector spaces E of infinite dimensions are considered. Let G be a subgroup of the orthogonal group of E acting on a set M. The ‘Lattice Method’ is a technique for classifying the orbits in M under G. We discuss the method in abstract terms and we illustrate it by means of three classification results showing that it is decisive to do a considerable amount of explicit calculations with vector subspace lattices.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 904-907 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Structure of “;Trichloro-diphenoxyphosphorane”The structure of ‘Trichloro-diphenoxyphosphorane’ synthesized by well-known and new methods is not a pentacoordinated phosphorus compound, but has the structure of tetraphen-oxyphosphonium hexachlorophosphate 4.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 231-236 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 47. Splitting of P—C-Bonds from Trisphosphoryl CompoundsHexaethyldimethylaminomethyl-trisphosphonate (2a) reacts with HCl or trimethylsilylbromid/water by splitting off one phosphoryl group, giving dimethylaminomethyl-bisphosphonic acid (7). The result of methylation of 2a depends on the reagent: with methyliodide one phosphoryl group is split off, and the ammonium salt 11a is formed, while with methyl toluene sulfonate or dimethylsulfate the expected quarternary ammonium salts 10b or 10c are formed. One phosphoryl group of 10c is split off under acidic as well as alkalinous conditions: acidic hydrolysis gives the bisphosphonic acid 15, while under alkalinous conditions the known ylid 16 is formed.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 314 (1972), S. 532-542 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2-Bis-[hydroxymethyl]-norbornen-(5) 5 läßt sich in bekannter Weise in Cyclische Derivate der phosphorigen Säure, wie z. B, das Diesterchlorid 6, den Triester 8a oder den Diester9 überführen; 6, 8a bzw. 9 wurden in verschiedener Weise weiter umgesetzt. Zum Unterschied von anderen cyclischen Phosphorigsäureestern reagiert 8a unter den Bedingungen der ARBUSOV- bzw. PERKOV-Reaktion mit verschiedenen C-Halogenverbindungen ausschließlich ohne Ringöffnung zu cyclischen Phosphonsäurederivaten, vermutlich wegen der Hinderung desnucleophilen Angriffs auf die Neopentyl-analogen CH2-Gruppen des Dioxaphosphanrings.  -  Die dargestellten Dioxan- bzw. Dioxaphosphanderivate liegen nach Ausweis der NMR-Spektren als Stereoisomerengemische vor.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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