Preparation and (13C)NMR spectroscopy of stereoregular poly(methacrylic acid)
β Scribed by A.J. Chapman; N.C. Billingham
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- English
- Weight
- 317 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Several procedures for synthesis of stereoregular poly(methacrylic acid) have been examined and the polymer characterized by (I~C)NMR. Using d 6 DMSO as solvent for spectroscopy gives better spectra than those previously obtained using aqueous solutions and stereoehemical splittings can be resolved in the methyl signals. Free-radical polymerization in toluene solution is a Bernouilli process giving mainly heterotactic/syndiotaetic polymer. Pobmers produced with free-radical initiation in aqueous solution have a higher, and pH dependent, content of syndiotactic triads. A previously described procedure for producing regular polymers by hydrolysis of poly(trimethylsilyl methacrylate) requires modification to produce isotactic contents of above 90Β°,,, and does not give truly syndiotactic polymer. In contrast, polymerization with 7-radiation can produce polymers v. ith close to 90'~,, of syndiotactic triads.
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