A new series of modified polyisophthalamides containing pendant furamido groups was prepared from S-(furamido)isophthalic acid and various aromatic diamines by the phosphorylation method. The chemical, physical and thermal properties of these polyamides were compared to those of the analogous unmodi
Polystyrylpyridine bearing pendant maleimide groups
β Scribed by John A. Mikroyannidis
- Book ID
- 103071061
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 299 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Poly(styrylpyridine) (PSP) bearing pendant maleimide groups in various concentrations was synthesized. The synthesis was based on the maleamic acid (MA) derived from 2-amino-4,6-dimethylpyridine and characterized by elemental analyses and by i.r, and ~H-NMR spectroscopy. MA was used as comonomer in various proportions (0, 10, 40, 70 and 100%) together with 2,6-dimethylpyridine to react with 1,4-benzenedicarbaldehyde in acetic anhydride. All polymers were characterized by i.r. spectroscopy and their curing behaviour was investigated by DTA. The onset temperature for curing of PSP fell with increasing concentration of maleimide groups in the resin. The thermal stabilities of cured resins were evaluated by dynamic TGA in N 2 and air and by isothermal gravimetric analysis. The attachment of maleimide groups to the PSP backbone reduced the initial decomposition temperature of cured resins but increased their anaerobic char yield at 800 Β°, when the proportion of maleimide moieties was below 40%.
π SIMILAR VOLUMES
Novel phenolic novolac resins, bearing maleimide groups and capable of undergoing curing principally through the addition polymerization of these groups, were synthesized by the polymerization of a mixture of phenol and N-(4-hydroxy phenyl)maleimide (HPM) with formaldehyde in the presence of an acid
## Abstract magnified image Diastereoselective Ξ³βdispiroiminolactone products **4a**, **4b**, **4c**, **4d**, **4e**, **4f**, **4g**, **4h**, **4i**, **4j**, **4k**, **4l**, **4m** were obtained from a condensation of the highly reactive 1:1 intermediate of isocyanides and acetylenic esters with a