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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2435-2447 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of fumaronitrile with triethylamine in bulk at 295-353 K gives in high yields dark-colored polymers. The polymerization occurs at one of the two nitrile groups and not at the (C—C) double bond. The kinetics of the reaction were investigated and the polymers characterized analytically.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 2 (1993), S. 917-927 
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The number of isomers ir,t for stacked polymeric phthalocyanines in which each phthalocyanine ring is tetrasubstituted or octasubstituted with two different substituents (each benzene moiety substituted with both substitutents) is determined to be \documentclass{article}\pagestyle{empty}\begin{document}$$ \mathop {\lim }\limits_{x \to \infty } i_{{\rm r,t}} = 2^m /16 $$\end{document} where m is the number of substituted phthalonitrile molecules incorporated into the polymer and x is the number of phthalocyanine macrocycles (degree of polymerization; m = 4x). Specifically, for a stacked polymeric phthalocyanine with x = 2; there exist 298 isomers. The stacked polymeric phthalocyanines with substituted phthalocyanine rings possess different symmetry groups (D2h, D2d, C4, C2V or CS E as sole symmetry operation). The results are valid for stacking of other macrocycles similar to phthalocyanine such as prophyrins.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 1 (1992), S. 187-191 
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As a result of their structure, polymeric phthalocyanines have four fractal dimensions for every size/shape/dilation combination. The construction of polymeric phthalocyanines resembles known fractals. A structure model of the polymer is extended. For infinitely large polymeric phthalocyanines, the same limiting value for the fractal dimensions (D = 2) was found to be valid for all structures.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Theory and Simulations 2 (1993), S. 503-515 
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Bridged polymeric phthalocyanines exist in different isomeric forms of varying symmetry. The number of isomers and the symmetry depends on the structure, i. e. the size and shape, of the polymeric phthalocyanine. Equations are derived for calculating the number of isomers for bridged polymeric phthalocyanines, and symmetry point groups for various shapes (linear, square, rectangular) are discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 1573-1586 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A model for describing the structural features such as degree of polymerization, size, and shape of polymeric phthalocyanines 2, 4, 6 is described. Analytical methods such as IR, titration of carboxylic end groups, and elemental analysis are used in the structure investigation. The results demonstrate that for polymeric phthalocyanines 2 with cyano end groups, prepared from 1,2,4,5-benzenetetracarbonitrile (1), the number of macrocycles (n) in the polymer is not higher than 7-9, and that linear polymers as well as polymers with two rows are possible. Polymers 6, prepared from bridged diphthalonitriles 5, are considerably larger showing a more two-dimensional structure. For polymeric phthalocyanines 4 with carboxylic end groups, prepared from 1,2,4,5-benzenetetracarboxylic acid derivatives 3, a linear structure with n = 4-9 is favoured. Literature results are examined in the light of the described model.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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