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  • Articles: DFG German National Licenses  (3)
  • palladium catalyst  (2)
  • aminolysis  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 1211-1218 
    ISSN: 0887-624X
    Keywords: three-component polycondensation ; π-allylpalladium complex ; bisallene ; aryl dihalides ; nucleophiles ; palladium catalyst ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel palladium-catalyzed three-component polycondensation of 1,2,10,11-dodecatetraene, 4,4′-diiodobiphenyl, and nucleophiles was carried out using various carbanions and amines as a nucleophilic part. The polymerization with various sodium diethyl malonates produced polymers in high yields. Particularly, no exo-double bond was detected in the polymers prepared from sodium diethyl malonates bearing substituents directly on the carbanion center. The ratios of E- and Z- isomeric units in the polymers were dependent on the structure of the nucleophiles used. Other carbanions with appropriate electron-withdrawing groups such as sulphones and ketones can be also used as a nucleophile for the present polycondensation. Within heteronucleophiles examined, cyclic amines were suitable to produce polymers in high yields. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1211-1218, 1997
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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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. 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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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 787-793 
    ISSN: 0887-624X
    Keywords: β-alkoxyenoate moieties ; hydrolysis ; aminolysis ; displacement of the main chain ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydrolysis and the substitution reaction of the main chain of the polymer having β-alkoxyenoate moieties in the main chain are described. The hydrolysis of the polymer prepared from 2,2-dimetylpropylene-1,3-bis(propiolate) and p-xylene glycol under acidic conditions proceeded smoothly to obtain diols in quantitative yield by the cleavage of both ester and vinyl ether moieties. On the other hand, carboxylic acids were obtained by the hydrolysis of the polymer under alkaline conditions. The aminolysis with pyrrolidine gave the β-aminoenoate by the selective fission of vinyl ether moieties in quantitative yield. Furthermore, a polymer having β-aminoenoate moieties in the main chain was obtained by the reaction with piperazine via the displacement of the main chain. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 787-793, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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