| Autor: |
Cancouët, Patrick, Daudet, Elodie, Hélary, Gérard, Moreau, Michel, Sauvet, Georges |
| Zdroj: |
Journal of Polymer Science Part A: Polymer Chemistry; 1 March 2000, Vol. 38 Issue: 5 p826-836, 11p |
| Abstrakt: |
Poly(hydrogenmethylsiloxane-co-dimethylsiloxane)s of various compositions have been prepared by cationic ring-opening polymerization of octamethylcyclotetrasiloxane (D4) and 1,3,5,7-tetramethylcyclotetrasiloxane (DH4) in the presence of hexamethyldisiloxane as end-blocker or by rearrangement of poly(hydrogenmethylsiloxane) in the presence of D4. These copolymers were examined by high resolution 1H NMR (500.13 MHz) and 29Si NMR (99.37 MHz) spectroscopies. Triad effects were observed by 1H and up to heptad effects by 29Si NMR. The chemical shifts were assigned for these stereosequences. The intensities of the triad signals were used to calculate the quantitative parameters describing the microstructure of the copolymer chains: number-average block length (&Lmacr;) and persistence ratio (η). The values of these parameters for copolymers prepared in various experimental conditions show that the time necessary for redistribution reactions (backbiting) is much larger than the time required to establish the equilibrium between linear polymer and cyclic oligomers. However, redistribution is fast enough to prevent the formation of block copolymers even in the case of the rearrangement of poly(hydrogenmethylsiloxane) in the presence of D4. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 826836, 2000 |
| Databáze: |
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