Macromolecules · 2008 · 71 citations · 21 references
Natural SciencesChemistryMaterials ScienceOrganic ChemistryPolymer ChemistryPolymer MaterialsLiquid Crystal MaterialsLiquid CrystalsPolymer CharacterizationPolymer PhysicsPolymer StructurePolymer Thin FilmsCrystallization Of Semicrystalline PolymersGlass TransitionGlass Transition StructureLiquid Crystal Phase BehaviorLiquid Crystal Phase TransitionsMonomer FunctionalityPolymer GlassesThermal Properties
We have synthesized homologous series of para -, meta -, and ortho -substituted aryl ether diamine monomers, with either 2, 3, or 4 ether linkages per monomer unit, and prepared their corresponding poly(ether imide)s with 3,3′,4,4′-biphenyl dianhydride (BPDA) and 3,3′,4,4′-oxydiphthalic dianhydride (ODPA). All polymers were obtained in high molecular weights and gave good quality films with expected mechanical and thermal properties. The ortho - and meta -substituted diamines gave fully amorphous polymers, whereas the para -based diamines resulted in semicrystalline polymers. The glass-transition temperatures ( T g ) drop in the order of para > ortho > meta, and the T g drops considerably as a function of the aryl ether content and appears to level off at four ether linkages. The T g values of our polymers were contrasted with a simple quantitative model and found to be in good agreement with the experimental results (±10 °C). BPDA in combination with an all para -substituted, aryl ether-based diamine (BPDA- P 3 ) forms a thermotropic liquid crystalline phase. Optical microscopy experiments confirm the presence of a nematic melt. Highly aligned films could easily be obtained by stretching the films in the liquid crystal phase, and XRD analysis of quenched films confirmed the presence of a highly aligned smectic A phase (SmA) with an order parameter ⟨ P 2 ⟩ = 0.87, indicating a high degree of molecular alignment. To the best of our knowledge, this is the first example of an all-aromatic liquid crystalline poly(ether imide). Dynamic mechanical thermal analysis (DMTA) showed that the para -aryl ethers display broad β-transitions (25–160 °C), whereas the meta - and ortho -series do not show β-transitions. All PEIs with 3 or 4 aryl ether linkages become thermoplastic in nature. The purpose of this systematic study is to provided a basic set of design rules toward the design and synthesis of all-aromatic poly(ether imide) architectures.
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