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  • 1960-1964  (5)
  • 1950-1954
  • 1920-1924
  • 1964  (5)
  • Catalysis  (3)
  • Oxides  (2)
  • 1
    Electronic Resource
    Electronic Resource
    The Reaction of Oxides with Water at High Pressures and TemperaturesDedicated to Prof. Dr. H. Brockmann on the occasion of his 60th birthday (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 47-54 
    Details
    ISSN: 0570-0833
    Keywords: Oxides ; Water ; High-pressure chemistry ; Hydrolysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of the oxides SiO2, MoO3, and WO3 with steam at temperatures between 400 and 700 °C and pressures of 5 to 500 atm were studied by means of the transfer method. The results were evaluated by a new method. In the system Sio2/H2O the formation of gaseous Si(OH)4, Si2O(OH)6, and [SiO2(OH)2]x was found to occur in three different water-density ranges. In the systems MoO3/H2O and WO3/H2O the gaseous compounds MoO2(OH)2 and WO2(OH)2, which were already known, exist up to densities of approximately 0.05g/cm3. At higher densities, at which the supercritical phase begins to show the properties of a liquid to an ever increasing extent, isopolymolybdic or isopolytungstic acids appear.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196400471
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Surface Oxides of Carbon (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 669-677 
    Details
    ISSN: 0570-0833
    Keywords: Surface chemistry ; Oxides ; Carbon ; Graphite ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On oxidation of graphitic carbon, acidic surface oxides (or hydroxides in the presence of water) are formed at the boundaries of the carbon layers. It was found that the reaction of oxygen with microcrystalline carbon at 400-450°C yields four groups of different acidities. One strongly acidic group and one weakly acidic carboxyl group have been detected, as well as a phenolic hydroxyl group; a carbonyl group is probably also present. With dissolved oxidizing agents, one equivalent of another strongly acidic carboxyl group is formed in addition at room temperature. The possible constitutions of the acidic surface oxides are discussed. Chemically detectable surface oxides are also formed on the surface of diamond. In the presence of oxygen at 800-900°C under reduced pressure, diamond is transformed into black carbon. Surface oxides play a part in this transformation.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196406691
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Proton Transfer, Acid-Base Catalysis, and Enzymatic Hydrolysis. Part I: ELEMENTARY PROCESSESPart II (Catalytic Mechanisms) will appear shortly in this journal.Dedicated to Dr. W. Foerst on the occasion of his 65th birthday (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 1-19 
    Details
    ISSN: 0570-0833
    Keywords: Proton transfer ; Catalysis ; Enzyme catalysis ; Hydrolysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton occupies a special position as a promoter and mediator in chemical reactions occurring in solution. Many reactions in organic chemistry are catalysed by acids or bases; likewise, most enzymes contain active groups which promote acid-base catalysis. To understand the reaction mechanisms involved, it is necessary to identify the elementary steps as well as their course in time. Systematic investigation of these elementary steps as well as their course in time. Systematic investigation of these elementary steps has become possible only with the development of new methods for studying very fast reactions. The present paper reviews the information obtained in this type of investigation. The result is a relatively complete picture of the elementary proton transfer mechanisms and a comprehensive description of the modes and laws of acid-base and enzymatic catalysis.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196400011
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  • 4
    Electronic Resource
    Electronic Resource
    The Mechanism of the Action of Organometallic CatalystsDedicated to Prof. Dr. Karl Winnacker on the occasion of his 60th birthday. (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 93-101 
    Details
    ISSN: 0570-0833
    Keywords: Organometallic catalysts ; Catalysis ; Reaction mechanisms ; Lithium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic investigations of the polyreaction of isoprene with organolithium compounds as initiators in n-heptane as solvent indicate the following sequence of reactions: 1. formation of an adduct between a monomeric form of the organolithium compound and the isoprene and 2. reaction of this adduct with an associated form of the organolithium compound with insertion of the isoprene. The adduct formation is considered to be due to chemisorption, and proof of such chemisorption of a monomer (ethylene) is also demonstrated for a homogeneous Ziegler-type catalyst. All the reactions can be formulated in the form of cyclic structures with electron-deficient character. Postulation of such ring structures explains the surprising values obtained for the frequency factors and equilibrium constants.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196400931
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  • 5
    Electronic Resource
    Electronic Resource
    Coordination Chemistry and Catalysis. Investigations on the Synthesis of Cyclooctatetraene by the Method of W. Reppe (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 185-191 
    Details
    ISSN: 0570-0833
    Keywords: Coordination modes ; Catalysis ; Cyclooctatetraenes ; Reppe chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relationship between the structure and the catalytic activity of nickel(II) complexes in the synthesis of cyclooctatetraene by the method of W. Reppe is discussed. The cyclotetramerization of acetylene takes place within labile Ni(II)-acetylene π-complexes. Inhibition tests have made it probable that four molecules of acetylene are grouped around the nickel ion in the transition state, in a configuration which favors the formation of the eight-membered ring.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196401851
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    Paper (German National Licenses)
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