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  • 1985-1989
  • 1965-1969  (6)
  • 1945-1949
  • 1820-1829
  • 1965  (6)
  • Alkylidenephosphoranes  (3)
  • Phosphorus  (3)
Material
Years
  • 1985-1989
  • 1965-1969  (6)
  • 1945-1949
  • 1820-1829
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 457-471 
    ISSN: 0570-0833
    Keywords: Color ; Azo compounds ; Azobisphosphoric acid ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Attempts to explain the surprising violet color of the new azobisphosphonic acid derivatives Y2OP—N=N—POY2 have led to the preparation and spectroscopic characterization of more than 60 azo compounds. The long-wavelength n → π* transitions on which the color depends exhibit regularities which justify the assumption of substitutent-specific absorption increments. The complex relation between color and constitution of azo compounds can be qualitatively explained with the aid of orbital models. Infrared and ultraviolet spectral data show that conjugation is inhibited by tetra-coordinated phosphorus (V). the π-system of these compounds therfore comprises only for atoms, P·N·N·P. The unexpected violet color of the phosphorus azo compounds can be ascribed to a π*/d orbital interaction. The substituent effects described have general significance, and n→π*transitions of other chromophores are similarly affected.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 583-587 
    ISSN: 0570-0833
    Keywords: Alkylidenephosphoranes ; Phosphonium salts ; Synthetic methods ; Phosphoranes ; Ylides ; Alkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phosphonium salts may be regarded as Bronsted acids, and alkylidenephosphoranes as the conjugate bases. Compounds of the two classes exist in equilibrium with each other. Phosphonium salts and alkylidenephosphoranes can be obtained by this “transylidation”. Other methods are also given for the preparation of members of both classes.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0570-0833
    Keywords: Alkylidenephosphoranes ; Phosphonium salts ; Synthetic methods ; Phosphoranes ; Ylides ; Alkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of alkylidenephosphoranes with compounds containing halogens can be used to prepare ylides, which can be converted in to useful products, e.g. by hydrolysis, by thermal decomposition, or by other reactions. Examples of such products are ketones including cyclic, unsaturated, and branched-chain ketones (including cyclic, unsaturated, and branched-chain ketones), carboxlic esters (including those of unsaturated, branched- chain, polyenecarboxylic, acetylenecarboxylic, and allenecarboxylic acids), and aldehydes.
    Additional Material: 10 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0570-0833
    Keywords: Alkylidenephosphoranes ; Phosphonium salts ; Synthetic methods ; Phosphoranes ; Ylides ; Alkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A few examples of preparatively useful syntheses using alkylidenephosphoranes and substances containing a C—N or C—C double bond are the preparations of olefins, allenes, pyran derivatives, and cyclopropane derivatives. Olefins, ketones, and monocyclic compounds can be obtained by autoxidation of alkylidenephosphoranes; α, β-dioxo compounds (including cyclicones) can be prepared by oxidation with peroxy-acids. Alkylidenephosphoranes can also be used for the synthesis of azines and Schiff bases. Of the many possibilities offered by the Wittig reaction, only the preparation of tritiated aldehydes and olefins will be considered.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 1023-1038 
    ISSN: 0570-0833
    Keywords: Heterocycles ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of heterocycles containing phosphorus is described. The chemical behavior of ring systems containing trivalent phosphorus is mainly determined by their phosphine character; heterocyclic behavior in the ordinary sense is shown by rings containing functional groups. Syntheses and reactions of cyclic compounds of pentavalent and hexavalent phosphorus are particularly interesting.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 1007-1013 
    ISSN: 0570-0833
    Keywords: Sulfur ; Selenium ; Tellurium ; Phosphorus ; Organometallic compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bond fission of molecular sulfur, selenium, and tellurium by lithiotriphenylmetal compounds (of Ge, Sn, Pb) is summarized. The products are suitable as starting materials for synthesis of new “ether analogues”. Transphenylation with tetraphenylstannane is interpreted as a high-temperature variant of the usual fission of chalcogen molecules by nucleophilic reagents. In principle, transphenylation can be applied also to other elements, as is illustrated for phosphorus. In the syntheses achieved, many of the tin-phosphorus compounds arising as intermediates can be isolated.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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