4.7 Article

Poly(ether imide)s from diamines with para-, meta-, and ortho-arylene substitutions:: Synthesis, characterization, and liquid crystalline properties

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MACROMOLECULES
卷 41, 期 7, 页码 2474-2483

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AMER CHEMICAL SOC
DOI: 10.1021/ma8000324

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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, drops considerably as a function of the aryl ether content and appears to level off at four ether linkages. The T, values of our polymers were contrasted with a simple quantitative model and found to be in good agreement with the experimental results (+/- 10 degrees C). BPDA in combination with an all para-substituted, aryl ether-based diamine (BPDA-P3) 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 beta-transitions (25-160 degrees C), whereas the meta- and ortho-series do not show beta-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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