Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1975-1979  (4)
  • 1979  (4)
Material
Years
  • 1975-1979  (4)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 5 (1979), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 5 (1979), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Acylation of the Phosphoryl Oxygen. I. Acyloxyphosphonium Salts from HMPT and Carboxylic Acid DerivatesAcylation equilibria with participation of acyloxyphosphonium ions exist in solutions of HMPT and carboxylic chlorides, or anhydrides, respectively, as can be shown by 31P-n.m.r. after trapping the counter ion with SbCl5. Moderately stable acyloxyphosphonium salts have been isolated for the first time by acylation of HMPT. In the alternative reaction of (Me2N)3P with CCl4 and carboxylic acids, acyloxyphosphonium salts are formed only after prolonged reaction times, due to the stability of the intermediate chlorotris-(dimethylamino)-phosphonium ion.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 450 (1979), S. 5-20 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Investigations of the Condensation Reactions of Mono-, Di-, and Trisilicic Acid by Trimethylsilylation and 29Si N.M.R. SpectroscopyThe condensation reactions of mono-, di- and trisilicic acid in acidic aqueous solution (CSiO2 = 0.5 m; pH = 2; T = - 2°C), obtained by hydrolysis of tetramethoxysilane, hexamethoxydisiloxane and octamethoxytrisiloxane resp., were quantitatively investigated in dependence of time. It could be shown that the monosilicic acid reacts across a mixture of di-, tri-, tetra-, cyclotetra- and bicyclohexasilicic acids to highpolymer products. In the solution of di- and trisilicic acid a partial hydrolysis to mono- and disilicic acid resp. occur simultaneous to the condensation reactions. By this way after short reaction times (about 20 min) in these solutions the same reaction products are present as in the monosilicic acid. The hydrolysis and condensation of the low molecular weight silicic acids were determined by equilibrium reactions which lead after about 6 h to constant mole ratios of the reaction products, independently of the type of silicic acid used in the initial solution. In all solutions no condensation products of uniform structure or molecular weight could be observed but always mixtures of silicic acids with a wide distribution of molecular weights. Even after 96 h of reaction time small amounts of mono-, di-, and trisilicic acid could be estimated.
    Notes: Die Kondensationsreaktionen der Mono-, Di- bzw. Trikieselsäure in saurerwäßriger Lösung (CSiO2 = 0,5 m; pH = 2; T = -2°C), hergestellt durch Hydrolyse von Tetramethoxysilan, Hexamethoxydisiloxan bzw. Octamethoxytrisiloxan, wurden in Abhängigkeit von der Zeit quantitative untersucht. Es wird gezeigt, daß die Monokieselsäure über ein Gemisch aus Di-, Tri-, Tetra-, Cyclotetra- und Bicyclohexakieselsäuren zu höhermolekularen Kieselsäuren reagiert. In, Di- und Trikieselsäurelösungen läuft parallel zu den Kondensationsreaktionen eine teilweise Hydrolyse unter Bildung von Mono- bzw. Dikieselsäure ab, so daß bereits nach kurzer Zeit die gleichen Reaktionsprodukte wie in der Monokieselsäurelösung auftreten. Die Hydrolyse und Kondensation der niedermolekularen Kieselsäuren werden durch Gleichgewichtsreaktionen bestimmt, die nach längeren Reaktionszeiten (etwa 6 h) zu konstanten Konzentrationsverhältnissen führen, die unabhängig von der Art der Ausgangskieselsäure sind. In allen Fällen werden keine molekulareinheitlichen Kondensationsprodukte, sondern stets Gemische von Kieselsäuren mit unterschiedlichem Kondensationsgrad beobachtet, in denen auch nach 96 h noch geringe Mengen Mono-, Di- und Trikieselsäure nachweisbar sind.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...