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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 6100-6101 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The configuration of citraconic anhydride units in p-chlorostyrene/citraconic anhydride copolymers prepared in methyl ethyl ketone at 50.0±0.1°C and the corresponding copolymer compositions and comonomer unit sequence distributions were determined over a range of comonomer feed mole fractions using 13C NMR spectroscopy. It was found that the ratio of Z (zusammen) to E (entgegen) configurations of citraconic anhydride units in these semi-alternating copolymers showed an overall tendency to increase with the degree of alternation of the monomer units.
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  • 3
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The configuration of maleic anhydride units in p-methoxystyrene-maleic anhydride copolymers prepared in methyl ethyl ketone at 50°C was studied using 13C NMR DEPT experiments. The ratio of cis (erythro) to trans (threo) configurations was found to increase with the tendency of the monomer units to alternate, remaining almost constant at approximately 1.33 when the mole fraction of maleic anhydride in the feed was larger than 0.30 and the monomer unit sequence was almost completely alternating. Also, para substitution on the styrene monomer units was found to greatly improve the resolution of the 13C NMR DEPT spectra for copolymers of p-methoxystyrene and p-chlorostyrene with maleic anhydride as compared with that of styrene-maleic anhydride copolymers.
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  • 4
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The configuration of maleic anhydride units in p-chlorostyrene/maleic anhydride copolymers prepared in methyl ethyl ketone at 50 ± 0.1°C and the corresponding comonomer unit sequence distributions were determined using the13C DEPT NMR sequence. It was found that the ratio ofcis (erythro) totrans (threo) configurations of maleic anhydride units increased with the degree of alternation of the comonomer units, reaching a constant value of approximately 0.73 when the comonomer units were almost completely alternating.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The configuration of citraconic anhydride units in p-methoxystyrene/citraconic anhydride copolymers prepared in methyl ethyl ketone at 50.0±0.1°C and the corresponding copolymer compositions and comonomer unit sequence distributions were determined over a range of comonomer feed mole fractions using13C NMR spectroscopy. It was found that the ratio ofZ (zusammen) toE (entgegen) configurations of citraconic anhydride units in these copolymers increased with the degree of alternation of the comonomer units, reaching a constant value of approximately 1.72 when the comonomer units were almost completely alternating and the mole fraction of citraconic anhydride units in the copolymers approached 0.50.
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The composition and sequence distribution of copolymers of maleic anhydride (MA) with p-methoxystyrene (p-MST) and p-chlorostyrene (p-CST) prepared in ethyl methyl ketone at 50 ± 0,1°C were analysed using 13C DEPT NMR techniques, in order to compare the applicability of composition and sequence distribution data to the study of the mechanism of copolymerisation using the terminal, penultimate and complex-participation models. In the case of the strongly alternating copolymerisation of p-MST with MA, the comparison of models on the basis of sequence distribution data was found to be better at separating each model in terms of its applicability, with the complex-participation model providing the best fit to the data. In the case of the less strongly alternating copolymerisation of p-CST with MA, neither method of comparison could clearly distinguish between the penultimate and complex-participation models.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 2001-2015 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The composition and monomer unit sequence distribution of copolymers of p-methoxystyrene (p-MST) with citraconic anhydride (CA) prepared in methyl ethyl ketone (MEK) at 50,0 ± 0,1°C were determined over a range of comonomer feed mole fractions using 13C NMR spectroscopy. The monomer units in these copolymers were found to display an increasingly strong tendency to alternate as the mole fraction of CA in the feed increases. The existence of a 1:1 charge-transfer complex formed between p-MST and CA in the feed was confirmed via UV spectroscopy and the equilibrium constant for complex formation was determined. The terminal, penultimate and complex-participation models were tested for applicability to the mechanism of copolymerisation for this comonomer system. On the basis of copolymer composition data, the penultimate and complex-participation models were found to provide each an adequate description of the mechanism of copolymerisation in the comonomer system via non-linear least squares methods. The inadequacies of the terminal and penultimate models in describing the copolymers were exposed more explicitly through an analysis of their comonomer unit sequence distributions using reactivity ratio related test functions.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2971-2978 
    ISSN: 0887-624X
    Keywords: free-radical copolymerization ; complex-participation ; penultimate effect ; 1:1 electron donor-acceptor complex ; copolymer composition ; copolymer sequence distribution ; Comppen model ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Comppen model for the mechanism of free-radical copolymerization has been developed to account for both penultimate effects and the participation of 1:1 electron donor-acceptor complexes during chain propagation. This was achieved by incorporating penultimate effects into the existing complex participation model of Cais, Farmer, Hill, and O'Donnell, using probability theory to derive new copolymer composition and sequence distribution equations that are solely functions of the reactivity ratios, the composition of the comonomer feed, and the equilibrium constant for 1:1 electron donor-acceptor complex formation. The model was applied to experimental data from styrene/maleic anhydride copolymers prepared in methyl ethyl ketone at 50°C over a wide range of comonomer feed compositions, using nonlinear least-squares curve fitting techniques to determine best estimates of the reactivity ratios. Copolymer compositions and sequence distributions for copolymers in this comonomer system were then predicted using the Comppen model and compared to those determined experimentally via 13C-NMR spectroscopy. © 1994 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 917-932 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The composition and monomer unit sequence distribution of copolymers of p-chlorostyrene (p-CST) with citraconic (α-methylmaleic) anhydride (CA) prepared in methyl ethyl ketone (MEK) at 50,0 ± 0,1°C were determined over a range of comonomer feed mole fractions using 13C NMR spectroscopy. The monomeric units in these copolymers were found to display a mild tendency to alternate, which increased as the mole fraction of CA in the feed increased. The existence of a 1:1 charge-transfer complex formed between p-CST and CA in the feed was confirmed via UV spectroscopy and the equilibrium constant for complex formation determined to be 0,10 ± 0,04 L/mol in MEK at ambient temperature. The terminal, penultimate, complex-participation and complex-dissociation models were each tested for applicability to the mechanism of copolymerisation for this comonomer system. On the basis of copolymer composition data, the penultimate, complex-participation and complex-dissociation models were each found to provide an adequate description of the mechanism of copolymerisation in the comonomer system via non-linear least squares methods. An analysis of the comonomer unit sequence distributions for these semi-alternating copolymers and the application of reactivity ratio related test functions to this data allowed applicability of the four models under investigation to be separated more explicitly, with the complex-dissociation model providing the best fit to the data.
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 15 (1994), S. 61-65 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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