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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1793-1801 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of two novel polyamide ligands 3 and 4, containing 2,17-diaza[3.3](6,6′)-2,2′-bipyridinophane or 6,6′-bis(2-picolylaminomethyl)-2,2′-bipyridine units as part of the polymer backbone, respectively, and of the appropriate diamide model compounds 1c and 2c is described. 1H-NMR and IR spectral data support the ligand structures; furthermore, 1H-VTNMR analysis on macrocyclic diamide 1c indicates a restricted rotation of the amide bonds at ambient temperature and suggests for this molecule a fixed syn conformation in solution, with a “face to face” arrangement of the dipyridinyl moieties. Model compound 2c and polyamide 4 form stable 1:1 complexes with transition metals Co(II), Ni(II), and Cu(II). Conversely, macrocyclic model 1c and polyamide 3 exhibit the unique property to specifically complex Cu(II), even in the presence of sizeable amounts of Co(II) and Ni(II). The IR spectral changes related to the ligands upon complexation are briefly discussed.
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2237-2247 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyamides and polyureas containing cyclic (1b, 1c, and 1d) or acyclic (2b, 2c, and 2d) bipyridinediyl diamino units in the polymer backbone were prepared. By introducing aliphatic or aromatic comonomers, it was possible to influence the degree of rigidity of the resulting polymers. In the synthesis of the polymers 2c and 2d two new azamacrocycles 5 and 6, respectively, were also produced and they were isolated and characterized. 1H-NMR and IR spectral data support the structure of the synthesized compounds. Thermal analysis data indicate that the polyureas posses lower PDT (polymer degradation temperature) values with respect to the corresponding polyamides.
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 65-79 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the isomorphous relationships existing among five crystalline polyaromatic polymers containing O, S, CH2 bridges, i.e., where Ph is phenyl, is reported. Appropriate series of oligomers corresponding to these polymers have also been prepared in order to investigate how the solid-state properties of the oligomers correlate with those of the polymers. A preliminary x-ray analysis is reported showing that the polymers are actually isostructural.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 3627-3637 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A number of alternating copolymers containing anthryl and aryl units in the polymer chain have been prepared by Friedel-Crafts arylation of the anthracene (polymer type B) or by condensation of 9,10-bis(chloromethyl) anthracene with opportune aromatic substrates (polymer type A). Polymers of type A were all found to contain 9,10-disubstituted anthracene units, but polymers of type B were found to contain 1,4-disubstituted anthracene units. Structure of the polymers were established through their NMR and ultraviolet spectra, and through analogy with appropriate model compounds. It has been found that the inclusion of anthracene units in the polymer chain yields higher melting and more soluble materials with respect to polybenzyls containing only aryl units. Anthracene units introduce, also, some interesting fluorescence characteristics in the polymers, which show intense emission at about 440 mμ.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2453-2464 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Properties of some linear oligobenzyls corresponding to polybenzyl, poly(2,5-dimethylbenzyl), and poly(2,3,5,6-tetramethyl-benzyl) systems are correlated to those of relative polymers. From infrared and x-ray diffraction data, evidence is found that oligomers tend to assume the same crystal structure of the polymer as early as teh tetramer or pentamer stage. Syntheses of oligomers are described. Linear, crystalline polymers, necessary for comparison with oligomers, have been prepared and characterized. Polymerization conditions have been explored to some extent; relevant data are tabulated and discussed.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2475-2490 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polycondensation reactions of benzyl chloride, α-chloroethylbenzene, and benzhydryl chloride in the presence of SnCl4 or AlCl3 as catalysts have been investigated in the temperature range between +80° and -135°C. Polycondensations of benzyl chloride and α-chloroethylbenzene are quite similar in the reaction kinetics and are thought to occur by the same displacement mechanism. Polycondensation of benzhydryl chloride, however, seems to involve the formation of benzhydryl carbonium ions. At low temperatures linear polymers tend to be formed, in contrast with branched polymers produced at room temperature. Steric effects are found to play a major role in protecting polymers from branching at lower temperatures.Polybenzyl polymers are found to be less linear than poly(-α-methylbenzyl), even when prepared at -135°C.
    Additional Material: 14 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2727-2737 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational equilibria of piperidine diamides derived from five cyclic 1,2-dicarboxylic acids (I-V) have been investigated by dipole moment measurements and a priori conformational energy estimates. Since these diamides represent the building blocks of the polyamides derived from the above cyclic diacids and piperazine or trans-2,5-dimethylpiperazine, the results obtained in the study of the models have been used to investigate the conformation of the polymers. The overall evidence suggests that cyclopentane, cyclohexane, and bicyclooctane piperazine polymers behave as rigid rods in which the structural units possess approximately the same conformational preference exhibited by the respective model diamides.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 11 (1973), S. 619-623 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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