## Abstract The reaction of methylhydroquinone with hexachlorocyclotriphosphazene in the presence of a base, 4βpicoline, in cyclohexane was investigated. Nuclear magnetic resonance spectroscopy, multiangle laser light scattering, and elemental analyses were performed on the product and two other re
Synthesis and characterization of poly(4-alkyl-4-methyl-2-azetidinone)s
β Scribed by Marc Fournier; Robert E. Prud'homme
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 152 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
Poly-β€-amides (nylons 3) were synthesized via the anionic polymerization of a series of 4-alkyl-4-methyl-2-azetidinones where the alkyl group is a methyl, ethyl, propyl, butyl, or pentyl. The "non-assisted" polymerization was conducted under vacuum, in the bulk, at 160Β°C, using potassium 2-pyrrolidonate as catalyst, whereas the "assisted" polymerization was carried in dimethylsulfoxide, at room temperature, using N-acetylpyrrolidinone-2 as activator but it gave no polymer with a propyl or bulkier side group. Side reactions occur in all cases. X-ray spectra showed that poly(4-alkyl-4methyl-2-azetidinone)s are amorphous with propyl, butyl, and pentyl groups, and semi-crystalline with methyl or ethyl substituents. Both semi-crystalline polyamides exhibit an extended planar zigzag conformation, with a fiber identity period along the c axis of 4.9 Γ . Glass transition temperatures, melting temperatures, and/or decomposition temperatures are also reported.
π SIMILAR VOLUMES
Methacrylate monomer containing a photodimerizable a,b-unsaturated ketone moiety was prepared and polymerized in ethyl methyl ketone at 70 Β°C using benzoyl peroxide as an initiator. The polymer was characterized by UV, IR, 1 H NMR and 13 C NMR spectra. The molecular weights (M w and M n ) of the pol