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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2097-2103 
    ISSN: 0887-624X
    Keywords: palladium catalyst ; allene derivatives ; nucleophile bearing aryl halides moieties ; multibranched polymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel polymerization method of allene derivatives with nucleophiles bearing aryl halide moieties (A-B type) is described. By the polymerization of hexylallene with malonates bearing an aryl iodide part, polymers consisting both of internal and exomethylene (exo) double bonds were obtained by mean of the coupling reaction of three different components in high yields. On the other hand, a polymer obtained from phenylallene was selectively composed of internal double bonds (E and Z). By the reaction of hexylallene with a malonate bearing two aryl halide moieties (A-B2 type), a multibranched polymer was also obtained. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2097-2103, 1997
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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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