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  • 1975-1979  (7)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 178 (1977), S. 1993-1999 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1H and 13C NMR spectra of 1,5-cyclooctadiene oligomers were investigated and compared with those of 1,4-polybutadiene. The oligomers were prepared with Rh2O7 as catalyst and fractionated by vacuum distillation or gel-permeation chromatography. It was found that each fraction consists of a mixture of steric isomers possessing cis and trans structures in different ratios. The 13C NMR spectra of oligomers with less than 24 carbons vary with ring size, which is explained in terms of ring strain effects. The 13C NMR spectra of oligomers with more than 28 carbons are identical with the spectrum of 1,4-polybutadiene. It resulted that the ratio of cis to trans structure in the oligomers decreases with increasing molecular weight from 70:30 (C16) to that in the cyclooctadiene polymer (40:60).
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 178 (1977), S. 1823-1832 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spin-decoupled 1H NMR and 13C NMR methods were presented for the determination of the cis-trans sequence distribution in polybutadiene. Poly(butadiene-2,3-d2) and cis-trans isomerized polybutadienes were used for the peak assignment and the resonance of methylene protons in cis-trans linkage could be described as an A2B2 system. The dyad and triad sequence distributions of cis-1,4 and trans-1,4 units were determined for isomerized, equibinary and lithium catalyzed polybutadienes, and polycyclooctadienes. The accuracy of the measurements was also studied comparing the results with those by infrared method.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3551-3558 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H-NMR spectra of polyisoprene were assigned using polymers of isoprene-1,1,4,4-d4, isoprene-1,1,5,5,5-d5, and isoprene-4,4-d2 polymerized with various catalysts. The methylene-proton signal at 2.1 ppm in cis-1,4 - and trans-1,4-polyisoprenes was divided into H4- and H1-proton signals; H4 resonated at 2.21 ppm in both cis-1,4 and trans-1,4 units whereas H1 resonated at 2.05, 2.21, and 2.15 ppm. Splitting due to the dyad sequences of 1,4 and 3,4 units was apparent. The methine-proton (H3) in a 3,4 unit showed a broad peak centered around 1.5 ppm in C6D6. The overlapping of this signal with the methyl-proton signals at 1.73 and 1.63 ppm resulted in some uncertainty in the determination of the microstructure of polyisoprene which contained a considerable amount of 3,4 unit.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 73-81 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C-NMR spectra of hydrogenated polyisoprenes were investigated. Polyisoprenes containing various ratios of 1,4 and 3,4 units were prepared with n-BuLi/Et2O and were hydrogenated by using p-toluenesulfonylhydrazide. 13C-NMR signals of the hydrogenated polymers were assigned for the triad sequences arising respectively from the 1, 4 and 3, 4 units of polyisoprenes. On the basis of these assignments it was confirmed that 1,4 and 3,4 units were randomly distributed in the polyisoprenes prepared with n-BuLi and that these polymers did not contain appreciable amounts of head-to-head or tail-to-tail 1,4 linkages.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3027-3029 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 16 (1978), S. 473-476 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 14 (1976), S. 335-338 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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