A four-step synthetic strategy was applied to achieve novel methacrylic monomers. 5-Norbornene-2,2-dimethanol was prepared from a Diels-Alder reaction of cyclopentadiene and acrolein, followed by the treatment of the adduct with an HCHO/ KOH/MeOH solution. The resulting 1,3-diol (1) was then acetali
Poly(methyl methacrylate) containing pyrrole moieties in the side chains
✍ Scribed by Manfred L. Hallensleben; Dietmar Stanke; Levent Toppare
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 353 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Two synthetic routes to copolymers 7 of methyl methacrylate (MMA) with 2-(N-pyrrolyl)ethyl methacrylate (PEMA, 11) are compared. Copolymerization of MMA (4) with 2-bromoethyl methacrylate (BEMA, 3) leads to a precursor copolymer 5. The reactivity ratios are close to unity (rMMA = 0,90, rBEMA = 0,92). The polymer-analogous reaction of 5 with N-pyrrolylpotassium (6) runs to 99% conversion of the BEMA units. The synthesis of PEMA (11) is presented. The reactivity ratios of copolymerization of this monomer (11) with MMA (4) are determined to rMMA = 1,05 and rPEMA = 1,65. Copolymers 7 are further characterized by 'H nuclear magnetic resonance, infrared spectroscopy, gel-permeation chromatography and differential scanning calorimetry.
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