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  • 2-vinyldibenzothiophene  (1)
  • Industrial Chemistry and Chemical Engineering  (1)
  • acetylene  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1853-1856 
    ISSN: 0887-624X
    Keywords: radical polymerization ; propargyl derivatives ; acetylene ; alkoxyallene ; isomerization polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2813-2819 
    ISSN: 0887-624X
    Keywords: styrene ; 2-vinyldibenzothiophene ; radical polymerization ; radical copolymerization ; monomer reactivity ratio ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A monomer having dibenzothiophene moiety, 2-vinyldibenzothiophene (1), was prepared by the Ni-catalyzed cross-coupling reaction of vinyl bromide with the Grignard reagent of 2-bromodibenzothiophene. The radical homopolymerization of 1 and the copolymerization with styrene were carried out at 60°C in toluene (1.0M) for 20 h using AIBN (5 mol %) as an initiator to obtain the corresponding polymers in high yields. Thermal analyses of the copolymers showed that both 10% weight loss and glass transition temperatures increase when increasing the content of 1 unit. The monomer reactivity ratio was evaluated as r1 = 2.55 (1) and r2 = 0.16 (styrene). © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2813-2819, 1997
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0268-2605
    Keywords: polymer ; organocobalt ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rearrangement reaction of an organocobalt polymer with cobaltacyclopentadiene moieties in the main chain (1) was carried out to yield a­new polymer bearing (η5-cyclopentadienyl) (η4-­cyclobutadiene)cobalt moieties in the main chain (2). For instance, a polymer (2) containing pure η4-cyclobutadienecobalt units was obtained as a yellow powder in 79% yield by the reaction of 1 in tetrahydrofuran (THF) at 110 °C for 1 h in a sealed tube. The polymer (2) obtained was soluble in organic solvents such as chloroform, THF and N,N-dimethylformamide and was quite stable under air. It showed good thermal stability and a weight loss of 5% was observed at 482 °C by thermogravimetric analysis (TGA). On the other hand, displacement of the triphenylphosphine ligands on the main chain of the organocobalt polymer (1), without rearrangement of the cobaltacyclopentadiene rings, was observed when the reaction was carried out in the presence of appropriate ligands such as P(n-Bu)3. The resulting ligand-exchanged polymer showed different properties in comparison with 1. For instance a polymer bearing tri-n-octylphosphine is soluble in n-hexane, which is a poor solvent for 1. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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