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  • 1950-1954  (10)
  • 1940-1944  (3)
  • 1
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European food research and technology 91 (1950), S. 195-199 
    ISSN: 1438-2385
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 6 (1951), S. 206-215 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The possibility of fractionation of p-cresol resins in organic solvents by addition of organic precipitating agents is proved by the average melting temperature, the analysis of carbon and hydrogen and the measuring of viscosity. The functions of \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{\eta _{sp} }}{{\rm c}} $\end{document}/c have minima, former observed with polyacrylic acid and desaminated albumen, but as far as we know. unknown at phenolic resins.The p-cresol resins were acetylated, transformed to urethanes by phenylisocyanate and methylated by diazomethene. Also the acetyl derivates and urethanes demonstrate the possibility of fractionation in organic solvents by organic precipitants.
    Notes: Die Möglichkeit der Fraktionierung von p-Kresol-Formaldehyd-Harzen in organischen Lösungsmitteln durch Zugabe von organischen Fällungsmitteln wird durch die mittlere Schmelztemperatur der Harz-Fraktionen, deren Elementaranalyse und durch ihr Viskositätsverhalten belegt. Die \documentclass{article}\pagestyle{empty}\begin{document}$ \frac{{\eta _{sp} }}{{\rm c}} $\end{document}/c-Funktionen zeigen Minima, die bei Polyacrylsäure und desaminierten Eiweißen schon beobachtet wurden, aber unseres Wissens bei Phenolharzen noch unbekannt sind.Es werden ferner Angaben gemacht über die Acetylierung, den Umsatz mit Phenylisocyanat zu Urethanen und die Methylierung mit Diazomethan. Auch die Untersuchung der Acetylderivate und Urethane zeigi. daß die Fraktionierung aus organischen Lösungsmitteln gelingt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 13 (1954), S. 210-222 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Different diacyl peroxides, hydroperoxides, dialkylperoxides and peracids are used as components of Fe··-redox-systems to polymerize styrene in benzene at 50° C. The conversions so obtained are compared with those of peroxide-induced polymerization. In cases of brominated peroxides one can calculate from the bromine-content of the polymers the incorporated catalyzer-fragments. No bromine can be found in the polymer if one uses brombenzoperacid; therefore if must be assumed, that the chain-initiation ensues through OH-radicals.
    Notes: Verschiedene Diacylperoxyde, Hydroperoxyde, Dialkylperoxyde und Persären werden als Komponenten von Eisen-Redox-Systemen zur Polymerisation von Styrol in Benzol bei 50° C benutzt. Die erzielten Umsätze werden mit denen bei peroxydischer Polymerisation verglichen. Bei bromhaltigen Peroxyden kann aus dem Bromgehalt der Polymeren auf die Zahl der eingebauten peroxydischen Bruchstücke geschlossen werden. Dabei Anwendung von Brombenzopersäre kein Brom in den Polymeren nachzuweiseu ist, muß angenommen werden, daß der Kettenstart durch OH-Radikale erfolgt.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 24 (1941), S. 100E 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 158 (1941), S. 186-199 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: In the polymerization of styrene and dimethyl butadiene 2,3 initiated by Fe2+ redox systems the peroxidal compound (diacyl peroxide) is permanently attached to the polymer. It is shown, that the number of incorporated, marked terminal groups in the polymerisation of styrene with p-bromobenzoylperoxide-Fe3+ benzoate-benzome is the same as in the peroxidal polymerization with p-bromobenzoyl peroxide. This evidence points to assuming that the peroxidal polymerization is also initiated by radicals which are formed by redox reaction between peroxide and monomer. In case of the polymer dimethyl butadiene all marked terminal groups which are formed in the Fe2+ redox catalized polymerization, are indicated to be ester groups.
    Notes: Bei der durch Eisen-Redox-Systeme ausgelösten Polymerisation von Styrol und von Dimethylbutadien -2.3 wird die peroxydische Komponente (Diacylperoxyd) in die Makromoleküle eingebaut. Es wird gezeigt, daß bei der Polymerisation des Styrols mit Dibrombenzoylperoxyd-Eisenbenzoat-Benzoin die Zahl der eingebauten, markierten Endgruppen die gleiche ist wie bei der peroxydischen Polymerisation mit Di-Brombenzoylperoxyd. Dies spricht dafür, daß auch die peroxydische Polymerisation durch Radikale ausgelöst wird, die bei einer Redox-Reaktion zwischen Peroxyd und Monomerem entstehen. Für das polymere Dimethylbutadien wurde nachgewiesen, daß alle markierten Endgruppen, die bei der eisen-redox-katalysierten Polymerisation gebildet werden, esterartig eingebaut sind.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 7 (1951), S. 46-61 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: This paper describes attempts to prepare soluble, rod-like molecules, the para-linked methyl-substituted polyphenylenes. The Ullmann reaction between 4.4′-di-iodo-3.3′-dimethyl-diphenyl and copper powder was carried out under varying conditions. The resulting soluble methylated polyphenylenes were fractionated and ultracentrifugal and osmotic pressure measurements indicated molecular weights up to 300000 for the highestmoleculare fractions. Cryoscopic measurements gave anomalous molecular weights. The results of the measurements of viscosity, sedimentation and diffusion are discussed with regard to the shape of these molecules. It appeared that the molecules obtained under these conditions, are neither rigid, nor rodlike. Side reactions probably give metalinked or branched products.
    Notes: Es werden Versuche geschildert, die zur Darstellung von löslichen, stäbchenförmigen Molekülen, nämlich para-verketteten, methylsubstituierten Polyphenylenen führen sollen. 4.4′-Dijod-3.3′-dimethyl-diphenyl wurde nach Ullmann mit Kupferpulver unter verschiedenen Bedingungen kondensiert und die erhaltenen löslichen, methylierten Polyphenylene fraktioniert. Ultrazentrifugale und osmotische Messungen ergeben für die höchstmolekularen Fraktionen Molekulargewichte bis zu 300000. Kryoskopische Untersuchungen liefern anomale Molekulargewichte. Die Ergebnisse der Viskositäts-, Sedimentations und Diffusionsmessungen werden im Hinblick auf die Gestalt der Moleküle diskutiert. Die unter den angewandten Reaktionsbedingungen erhaltenen Produkte sind vermutlich keine starren, stäbchenförmige Gebilde. Durch Nebenreaktionen entstehen vielleicht meta- Verknüpfungen oder Verzweigungen.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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