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  • Chemistry  (42)
  • GEOPHYSICS  (3)
  • 1990-1994  (31)
  • 1980-1984  (9)
  • 1960-1964  (3)
  • 1925-1929  (2)
  • 1
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    Report on the international Cambodian crater expedition, 1992 (1992)
    In:  CASI
    Details
    Publication Date: 2013-08-31
    Description: It has been proposed that Tonle Sap, a lake in Cambodia, 100 km long and 30 km wide, marks the location of an elongate basin formed by the oblique impact of a comet or asteroid. The impact is considered to have produced melted ejecta found now as tektites over much of southeast Asia and Australia. The location of the lake, its approximate age, its size, and the orientation of its long axis (toward Australia) are consistent with this hypothesis. Our scientific objectives were to find impact or shock metamorphosed rocks unambiguously related to the Tonle Sap basin, to collect samples of rocks that may represent those melted to produce Australasian tektites, and to learn as much as possible about Cambodian geology. Using 1:200,000-scale geologic maps with fairly detailed descriptions of the rock units, we selected a number of acceptable 'phnoms' (hills that rise abruptly out of the surrounding plain) that may contain rocks affected by the postulated Tonle Sap impact. A map of central Cambodia is shown, and the locations of sites where samples were collected are indicated. A list of those sites, together with a description of the rocks reported to be present at each site, is given. No obviously shock-metamorphosed or suevite-like rocks were observed. Recent alluvium surrounding Tonle Sap is judged to be lake sediment deposited when the lake surface was at a higher elevation.
    Keywords: GEOPHYSICS
    Type: Lunar and Planetary Inst., International Conference on Large Meteorite Impacts and Planetary Evolution; p 36-37
    Format: application/pdf
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    NASA TECHNICAL REPORTS
  • 2
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    Descriptions and preliminary interpretations of cores recovered from the Manson Impact Structure (Iowa) (1993)
    In:  Other Sources
    Details
    Publication Date: 2019-01-25
    Description: A core drilling program initiated by the Iowa Geological Survey Bureau and U.S. Geological Survey in 1991 and 1992 collected 12 cores totalling over 1200 m from the Manson Impact Structure, a probable K-T boundary structure located in north-central Iowa. Cores were recovered from each of the major structural terranes, with 2 cores (M-3 and M-4) from the Terrace Terrane, 4 cores (M-2, M-2A, M-6, and M-9) from the Crater Moat, and 6 cores (M-1, M-5, M-7, M-8, M-10, and M-11) from the Central Peak. These supplemented 2 central peak cores (1-A and 2-A) drilled in 1953. The cores penetrated five major impact lithologies: (1) sedimentary clast breccia; (2) impact ejecta; (3) central peak crystallite rocks; (4) crystalline clast breccia with sandy matrix; and (5) crystallite clast breccia with a melt matrix. Descriptions and preliminary interpretations of these cores are presented.
    Keywords: GEOPHYSICS
    Type: Lunar and Planetary Inst., Twenty-fourth Lunar and Planetary Science Conference. Part 1: A-F; p 35-36
    Format: text
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    NASA TECHNICAL REPORTS
  • 3
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    Manson impact structure, Iowa: First geochemical results for drill core M-1 (1993)
    In:  CASI
    Details
    Publication Date: 2019-06-28
    Description: The Manson Impact Structure is a large complex impact crater centered ca. S km north of the town of Manson, Iowa. It is the largest intact impact structure recognized in the United States (35 km in diameter). Its Ar-40/Ar-39 age is indistinguishable from that of the Cretaceous-Tertiary (K-T) boundary. The Manson structure may be one element of the events at the K-T boundary. The crater is completely covered by Quaternary glacial sedimentary deposits that are normally underlain by Cretaceous clastic sediments and flat-lying carbonate sediments of Phanerozoic age, as well as Proterozoic red clastic, metamorphic, volcanic, and plutonic rock sequences. The study of a reflection seismic profile, provided by Amoco, was critical in interpreting the structure. In the 35 km diameter zone that marks the extension of the crater the normal rock sequence is disturbed due to the impact, and at the center of the structure granitic basement rocks are present that have been uplifted from about 4 km depth. Our studies consist of detailed petrological and geochemical characterization of all cores, with emphasis on a detailed description of all rock types found in the core samples and their relationship to target rocks. Geochemical data on samples from the Manson M-1 core are presented.
    Keywords: GEOPHYSICS
    Type: Lunar and Planetary Inst., Twenty-Fourth Lunar and Planetary Science Conference. Part 2: G-M; p 811-812
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    NASA TECHNICAL REPORTS
  • 4
    Electronic Resource
    Electronic Resource
    A New Route to Alkoxy Radicals  -  Photochemical Reactions with (Alkylperoxy)cobaloximes (1991)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 387-390 
    Details
    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
    URL: http://dx.doi.org/10.1002/cber.19911240223
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  • 5
    Electronic Resource
    Electronic Resource
    Polar Effects in Halogen Abstraction Reactions of Alkyl Radicals (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1777-1779 
    Details
    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
    URL: http://dx.doi.org/10.1002/cber.19921250734
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  • 6
    Electronic Resource
    Electronic Resource
    What is Different in Photochemical Reactions of Primary and Secondary Alkylcobaloximes with and without Radical Traps? (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1187-1191 
    Details
    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
    URL: http://dx.doi.org/10.1002/cber.19931260519
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  • 7
    Electronic Resource
    Electronic Resource
    Preparation and Properties of Alkylbis(dimethylglyoximato)rhodium(III) ComplexesDedicated to Professor Dr. Klaus Hafner on the occasion of his 65th birthday. (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1193-1200 
    Details
    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
    URL: http://dx.doi.org/10.1002/cber.19931260520
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  • 8
    Electronic Resource
    Electronic Resource
    Zum Konformationsverhalten substituierter Benzoesäurephenylester - Molekül- und Kristallstruktur der nematogenen Verbindung 4-n-Pentoxybenzoesäure-4′-(ß-cyanethyl)-phenylester (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 742-752 
    Details
    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
    URL: http://dx.doi.org/10.1002/prac.19833250508
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  • 9
    Electronic Resource
    Electronic Resource
    Zum Konformationsverhalten isomerer Phenylpyrimidine  -  Molekül- und Kristallstruktur von 5-Chlor-2-(4-n-hexyloxyphenyl)-pyrimidin (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 489-495 
    Details
    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
    URL: http://dx.doi.org/10.1002/prac.19833250319
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  • 10
    Electronic Resource
    Electronic Resource
    Two dimensional TLC determination of PAH in diluted automobile exhaust gasesBased on a paper delivered at the 2nd International Symposium on Instrumental High Performance Thin Layer Chromatography, May, 1982, at Interlaken. (1982)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 5 (1982), S. 489-494 
    Details
    ISSN: 0935-6304
    Keywords: Thin-layer chromatography ; Gas chromatography ; Exhaust gas emissions ; Polycyclic aromatic hydrocarbons (PAH) ; Dilution tunnel ; Langmuir adsorption model ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method is described for the determination of polycyclic aromatic hydrocarbons (PAH) in the diluted exhaust gas of diesel vehicles. Sampling is done by drawing off proportional streams from the dilution tunnel. The particulates deposited on filters are sublimed, and the sublimate is purified and prefractionated on silica gel. Further separation and quantitative determination of the PAH is performed by two dimensional TLC in conjunction with In situ fluorescence spectrometry. Results of theoretical considerations and experimental data on the distribution of the emitted PAH between particulate matter and the corresponding gas phase in diluted exhaust are presented. A modified Langmuir adsorption model is used to explain the effects of dilution ratio and sample temperature in the dilution tunnel. Comparison of the emission values for PAH obtained from diluted and undiluted exhaust shows good agreement. Furthermore, the PAH contents of the exhaust gas of several diesel-engined cars are also compared for various driving cycles.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240050907
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