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  • Chemistry  (42)
  • General Chemistry  (4)
  • LUNAR AND PLANETARY EXPLORATION  (4)
  • 1990-1994  (30)
  • 1980-1984  (11)
  • 1960-1964  (3)
  • 1925-1929  (2)
  • 1
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    Unknown
    In:  Other Sources
    Publication Date: 2019-01-25
    Description: The Moon's center of mass is displaced from its center of figure about 2 km in a roughly earthward direction. Most maria are on the side of the Moon which faces the Earth. It is assumed that the Moon was initially spherically symmetric. The emplacement of mare basalts transfers mass which produces most of the observed center of mass displacement toward the Earth. The cause of the asymmetric distribution of lunar maria was examined. The Moon is in a spin orbit coupled relationship with the Earth and the effect of the Earth's gravity on the Moon is asymmetric. The earth-facing side of the Moon is a gravitational favored location for the extrusion of mare basalt magma in the same way that the topographically lower floor of a large impact basin is a gravitationally favored location. This asymmetric effect increases inversely with the fourth power of the Earth Moon distance. The history of the Earth-Moon system includes: formation of the Moon by accretion processes in a heliocentric orbit ner that of the Earth; a gravitational encounter with the Earth about 4 billion years ago resulting in capture of the Moon into a geocentric orbit and heating of the Moon through dissipation of energy related to tides raised during close approaches to the Earth(5) to produce mare basalt magma; and evolution of the Moon's orbit to its present position, slowly at first to accommodate more than 500 million years during which magmas were extruded.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar Planetary Inst. Conf. on the Origin of the Moon; p 32
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  • 2
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    In:  Other Sources
    Publication Date: 2019-08-27
    Description: Harris (1993) in his review of the paper on Corvid meteoroids by Hartung (1993) questions the validity of the latter's analysis of possible commensurability relationships involving the periods of the heliocentric orbits of the earth-moon system and possible Giordano Bruno impact-derived Corvid meteoroids. Harris establishes upper limits for dispersion velocities by considering three regimes. His argument is that these maximum dispersion velocities are so low that their natural occurrence is implausible. Hartung infers that there may exist a permitted class of orbits which have periods longer than 1.02 yr and which once were filled with large ejected masses with dispersion velocities high enough to satisfy Harris' plausibility criterion, but not so high as to exceed his maximum acceptable dispersion velocities given in the lower curve he adduces.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Journal of Geophysical Research (ISSN 0148-0227); 98; E5; p. 9151, 9152; Comme
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  • 3
    Publication Date: 2019-07-13
    Description: The Manson impact structure (MIS) in Iowa is an excellently preserved complex crater that formed 65.7 Ma ago at the K/T boundary. Drill and seismic data have been used to identify three primary terranes within the 35-km diameter crater: (1) an outermost ring graben composed of listric normal fault blocks that structurally preserve Paleozoic and Cretaceous strata, impact ejecta, and possibly earliest Tertiary lake sediments; (2) a crater moat region of slumped and fallback materials overlain by Tertiary lake sediments in most areas; and (3) a central peak of uplifted basement rock capped in many areas by impact breccia. It is argued that concentrations of Ir at a K/T boundary exposure near Gubbio, Italy and clasts of glass reported from the K/T boundary in Haiti are consistent with possible production in the MIS.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar and Planetary Science Conference; Mar 18, 1991 - Mar 22, 1991; Houston, TX; United States
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  • 4
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    In:  Other Sources
    Publication Date: 2019-07-13
    Description: Lunar rock surfaces exposed at or just below the lunar surface are considered as detectors of the solar wind, solar flares and solar-derived magnetic fields through their interactions with galactic cosmic rays. The degradation of the solar detector capabilities of lunar surface rocks by meteoroid impact erosion, accreta deposition, loose dust, and sputtering, amorphous layer formation and accelerated diffusion due to solar particles and illumination is discussed, and it is noted that the complex interactions of factors affecting the outer micron of exposed surface material has so far prevented the development of a satisfactory model for a particle detector on the submicron scale. Methods for the determination of surface exposure ages based on the accumulation of light solar wind noble gases, Fe and Mg, impact craters, solar flare tracks, and cosmogenic Kr isotopes are examined, and the systematic variations in the ages determined by the various clocks are discussed. It is concluded that a means of obtaining satisfactory quantitative rate or flux data has not yet been established.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Conference on The ancient sun: Fossil record in the earth, moon and meteorites; Oct 16, 1979 - Oct 19, 1979; Boulder, CO
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 387-390 
    ISSN: 0009-2940
    Keywords: Peroxy compounds ; Cobaloximes ; Oxygen insertion ; Radicals, alkoxy ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkoxy radicals have been generated by photochemical reactions of (alkylperoxy)cobaloximes 1. The occurrence of alkoxy radicals has been proved by characteristic cyclization and β-scission reactions of the reactive intermediates.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1777-1779 
    ISSN: 0009-2940
    Keywords: Polar effects ; Radical clock ; Cobaloximes, alkyl ; Radicals, alkyl ; Chlorine abstraction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a series of structurally similar alkyl radicals 1a-c the tertiary 1,1-dimethyl-5-hexenyl radical 1c reacts 30 times faster with carbon tetrachloride than the primary 5-hexenyl radical 1a. The reactivity of the secondary 1-methyl-5-hexenyl radical 1b aligns itself in between the primary and the tertiary radical 1a and 1c. The results indicate that the increasing nucleophilicity of the alkyl radicals is the major factor contributing to the reactivity.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1187-1191 
    ISSN: 0009-2940
    Keywords: Cobaloximes, alkyl- ; 5-Hexenyl, cyclization to cyclopentylmethyl ; Radicals, alkyl ; Abstraction of bromine and chlorine ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemical cyclization and halogen abstraction reactions of secondary alkylcobaloximes 1b and 1d compared to their primary counterparts 1a and 1c show an enhanced reactivity of secondary alkylcobaloximes: Thus, cyclohexylcobaloxime 1d reacts 13 times faster with CCl4 than n1-hexylcobaloxime 1c, 6-hepten-2-yl-cobaloxime 1b rearranges 58 times faster to its cyclopentylmethyl isomer 4b than 5-hexenylcobaloxime 1a. Although free alkyl radicals are reactive intermediates in photolytic conversions of alkylcobaloximes 1 in organic solvents, the presence of BrCCl3 or bromobenzene in photoreactions of primary alkylcobaloximes 1a and 1c seems to cause a more efficient homolytic cleavage of the Co - C bond.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0009-2940
    Keywords: Alkylrhodoximes ; Radicals, alkyl ; Halogen abstraction ; Carbon-carbon bond formation ; Stereochemistry ; Photoreactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Primary, secondary, and tertiary alkylrhodoximes 1 were prepared from alkyl bromides and tosylates 4 and the trans1-dichlororhodium complex 3. X-ray crystallography of the previously unknown tert1-butylrhodoxime 1k reveals structural features of this tert-s̰1-alkylrhodium compound. Photochemical homolytic cleavage of the Rh - C bond in alkylrhodoximes 1 only occurs in the presence of efficient radical traps which allow further mechanistic studies.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Conformational Behaviour of Substituted Phenylbenzoates - Molecular and Crystal Structure of the Nematogenic Compound 4′-(ß-Cyanoethyl)-phenyl-4-n-pentoxybenzoateThe title compound crystallizes in the monoclinic space group P21/n with a = 1567.6(2) pm, b = 915.5(1) pm, c = 1459.1(1) pm, β = 115.30(1)°, and four molecules per unit cell. The structure has been solved by direct methods and refined to R = 0.104. The molecules adopt a markedly stretched form and show a parallel arrangement of their long axes in the crystal lattice. The molecular and crystal structure is discussed in relation to the mesomorphic behaviour of the compound.A theoretical conformational analysis has been performed for the isolated phenylbenzoate molecule using the EPEN/2 method, its results are compared with the experimental torsion angles in a series of substituted phenylbenzoates.
    Additional Material: 6 Ill.
    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 325 (1983), S. 489-495 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Conformational Behaviour of Isomeric Phenyl Pyrimidines  -  Molecular and Crystal Structure of 5-Chloro-2-(4-n-hexyloxyphenyl)-pyrimidineThe title compound crystallizes in the triclinic space group P1 with a = 979.6(1) pm, b = 1048.8(3) pm, c = 1629.9(1) pm, α = 89.51(1)°, β = 100.62(1)°, γ = 71.50(1)° and four molecules per unit cell. The structure has been solved by direct methods and refined to a final R value of 0.058. The molecules adopt a fully stretched and nearly planar form and show a parallel arrangement in the crystal lattice. The results are discussed in relation to the conformational and mesomorphic behaviour of isomeric substituted phenyl pyrimidines.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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