## Abstract A series of poly(ether ester)s containing different H‐bonding units (amide, carbamate, urea) was prepared by polycondensation in bulk, using Ti(OBu)~4~ as a catalyst. The copolymers were obtained starting from PEG1000, 1,4‐butanediol, and a symmetrical, bis‐ester terminated monomer carr
Synthesis of poly(enaryloxynitrile)s containing styrylpyridine segments
✍ Scribed by Ioakim K. Spiliopoulos; John A. Mikroyannidis
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 530 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0032-3861
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✦ Synopsis
New poly(enaryloxynitrile)s bearing styrylpyridine segments were synthesized by interracial polycondensation of p-bis(1-chloro-2,2-dicyanovinyl)benzene with various bisphenols such as 6-(4-hydroxystyryl)-3-hydroxypyridine (HSHP), 2,6-di(4-hydroxystyryl)pyridine and 2-(4-h2(droxystyryl)-8-hydroxyquinoline. They were characterized by viscosity, elemental analysis, FTi.r., J H and 3C n,m.r., X-ray, d.t.a., t.m.a., t.g.a, and isothermal gravimetric analysis. The polymer prepared from HSHP was crystalline and had a Tg at 270°C. The other polymers were amorphous and showed TgS at 200-210°C and softening at 235-247°C. All the polymers displayed an enhanced solubility in common organic solvents. Upon heat-curing, crosslinked polymers were obtained which were stable up to 370-397°C in N2 and afforded anaerobic char yields of 76-80% at 800°C.
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