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  • Articles: DFG German National Licenses  (17)
  • Chemistry  (17)
  • alkoxyallenes  (2)
  • 11
    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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  • 12
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2589-2592 
    ISSN: 0887-624X
    Keywords: polymer reaction ; oxidation ; push-pull olefin ; electron-deficient olefin ; vinyl sulfone ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation of a polymer (1) having β-alkylmercaptoenoate moieties in the main chain by m-chloroperbenzoic acid (MCPBA) is described. Oxidation of 1 proceeded selectively to give polymers having vinyl sulfoxide or vinyl sulfone moieties in the main chain by using an appropriate amount of MCPBA. In the case of 1.1 equiv of MCPBA (relative to the sulfur atom), a polymer (4) having vinyl sulfoxide moieties selectively in the main chain was obtained in quantitative yield without side reactions. Likewise, a polymer (5) having vinyl sulfone moieties was obtained in quantitative yield by using 2.6 equiv of MCPBA. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2589-2592, 1998
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1597-1604 
    ISSN: 0887-624X
    Keywords: polyaddition ; β-substituted bispropiolates ; diols ; tri-n-butylphosphine-catalyst ; conjugate addition ; β-alkoxyenoates ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tri-n-butylphosphine-catalyzed polyadditions of activated internal diynes (bifunctional β-substituted propiolate, 1B and 1C) with diols are described. Although a terminal bispropiolate (1A) could not produce soluble polymers, with secondary diols, the polyaddition of 1B or 1C with primary as well as secondary diols gave corresponding polymers (3, only composed of E isomeric units) in high yield. The rate of the present polyaddition was estimated by a model reaction of benzyl alcohol with methyl 2-heptynoate (4), from which the introduction of alkyl groups at the β-position of propiolate moieties was found to decrease the rate of the reaction by 80 times. Furthermore, the rate-determining step on this polymerization system was speculated to be a protonation step of zwitterionic intermediates with protons from diols. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 14
    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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  • 15
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1491-1494 
    ISSN: 0887-624X
    Keywords: sulfonyl isocyanate ; acrylamide ; hydrogen-transfer polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 19 (1998), S. 493-497 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The cationic initiation activity of derivatives of S-methylsulfonium salts has been evaluated in the cationic polymerization of glycidyl phenyl ether (1). These initiators are soluble in 1 and capable of initiating the cationic polymerization of 1 on heating, except for methyltetrahydrothiophenium tetrafluoroborate (6) (r.t. -160°C). Among them, methyldiphenylsulfonium tetrafluoroborate (4) shows moderate thermal latency, that is the polymerization of 1 occurs efficiently at 160°C but not below 80°C.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 17
    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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