Synthesis and properties of polyesters of isomeric poly(oxynaphthyleneoxy‐2‐bromoterephthaloyl)s
- 1 June 1989
- journal article
- research article
- Published by Wiley in Journal of Polymer Science Part A: Polymer Chemistry
- Vol. 27 (7) , 2291-2303
- https://doi.org/10.1002/pola.1989.080270713
Abstract
A series of aromatic polyesters were prepared from 2‐bromoterephthalic acid and naphthalenediol isomers. Only the polymers obtained from 1,4‐, and 1,5‐ and 2,6‐naphthalenediols were thermotropic nematogens and those from bent naphthalenediols were not liquid crystalline. Only the polyesters derived from 1,4‐, 1,5‐, and 2,6‐naphthalenediols were semicrystalline. The melting temperatures ranged from 319 to 374°C depending on the structure of naphthalenediol moiety. The glass transition temperature, Tg, ranged from 95 to 168°C. TGA studied revealed that the polyesters have fairly good thermal stabilityKeywords
This publication has 7 references indexed in Scilit:
- Properties of aromatic copolyesters derived from p-hydroxybenzoic acid, terephthalic acid, and naphthalenediol isomersMacromolecules, 1989
- Properties of poly(p-phenylene terephthalates) prepared from 2-nitro- and 2-bromoterephthalic acids and substituted hydroquinonesMacromolecules, 1987
- Thermotropic polyesters with main chain isomeric naphthylene, trans‐1,4‐cyclohexylene, and 2,5‐pyridinediyl units: The importance of the order of ester linkages in the mesogenic unitsJournal of Polymer Science Part A: Polymer Chemistry, 1987
- Nematogenic polymers having rigid chains. 1. Substituted poly(p-phenylene terephthalates)Macromolecules, 1985
- Liquid crystal polymers. XVIII. Comparison of the properties of aromatic polyesters with different mesogenic units and a common flexible spacerJournal of Polymer Science: Polymer Chemistry Edition, 1984
- Über 4′,5′,4″,5″-Tetraphenyl-(difurano-3′,2′:1,2; 2″,3″:3,4-naphthalin) und seinen AbbauMonatshefte für Chemie / Chemical Monthly, 1950
- Zur Kenntnis der aus dem 1,5-Dioxynaphtalin beim Erhitzen mit Kaliumbicarbonat unter Druck entstehenden DicarbonsäureMonatshefte für Chemie / Chemical Monthly, 1922