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  • 1970-1974  (9)
Materialart
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of organic chemistry 37 (1972), S. 2823-2826 
    ISSN: 1520-6904
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 12 (1974), S. 605-606 
    ISSN: 0360-6384
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 571-574 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 3503-3508 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Copolymers of phenylvinylene carbonate with styrene and p-chlorostyrene are readily prepared with radical initiators. The carbonate portion of the copolymers has been hydrolyzed to a 1,2-glycol which was then oxididatively cleaved with periodate-perman-ganate to produce a polymer with carboxyl and keto endgroups. Block copolymers were then prepared by conversion of the carboxyl groups to an acid chloride, followed by coupling with diols or a diamine.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2293-2308 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Optically active vinyl p-tolyl sulfoxide was synthesized and copolymerized with styrene to produce an optically active copolymer. The question of the configuration of sulfur in a sulfoxide when adjacent to a radical site is discussed. The configuration of sulfur in a sulfoxide is proven to be nonplanar when adjacent to an anionic site.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2713-2725 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Aromatic polyesters of 3,5-di-tert-butyl-4-hydroxybenzoic acid and 3,5-diisopropyl-4-hydroxybenzoic acid were prepared. The polymers were found to be high-melting but largely insoluble in organic solvents. The polymer based on 3,5-di-tert-butyl-4-hydroxy-benzoic acid was not degraded to monomer by sulfuric acid. A number of new aromatic polyesters were also prepared. Several new monomers for aromatic polyesters were synthesized, including bis(2,5-di-tert-butyl-4-carbophenoxyphenyl)terephthalate, m- and p-phenylene bis(3,5-di-tert-butyl-4-hydroxybenzoate), bis(2,6-di-tert-butyl-4-chlorocarboxyphenyl)terephthalate, and m-phenylene bis(3,5-diisopropyl-4-hydroxybenzoate). An aromatic polyester prepared from bis(2,6-di-tert-butyl-4-chlorocarboxyphenyl) terephthalate and resorcinol had a ηinh (trichloroethylene) of 1.05 (0.5%, 30°C) and a possible melting point of 330°C (DSC). Tough, creasable films could be cast from trichloroethylene solution of this polymer. Attempts to observe or to trap the keto-ketene that might result when 3,5-di-tert-butyl-4-hydroxybenzoyl chloride is treated with base were unsuccessful.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 3667-3670 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 2487-2492 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 10 (1972), S. 3469-3487 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The syntheses of N-2-phenylallylacrylamide (I) and N-ethyl-2-phenallylacrylamide (II) are described. Both monomers can be polymerized with radical initiators to form cyclopolymers although complete cyclization does not occur. Lewis acids (ZnCl2 in the case of I, Et1.5AlCl1.5 in the case of II) result in the formation of higher molecular weight polymers in a shorter period of time. Polymers of I and II have been hydrolyzed to polyampholytes. The copolymerization of α-methylstyrene-acrylamide in the presence of azobisisobutyronitrile (AIBN) and ZnCl2 leads to the formation of a 1:1 copolymer, whereas styrene-acrylamide under the same conditions give a copolymer slightly dependent upon the monomer feed composition. Attempted cyclopolymerization of N-allylacrylamide (monomer I without the phenyl group) with ZnCl2-AlBN was not successful, only crosslinked polymer being obtained. An explanation is offered for the fact that I does not form a perfect cyclopolymer, although the α-methylstyrene-acrylamide system forms a 1:1 copolymer.
    Zusätzliches Material: 10 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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