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The effect of flexible spacer length on the phase transitions and mesophase structures of main-chain thermotropic liquid-crystalline polyesters having bulky pendent side groups was investigated using differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), and polarizing optical microscopy (POM). For the investigation, a homologous series of poly[(phenylsulfonyl)- p -phenylene alkylenebis(4-oxybenzoate)]s (PSHQ n ) having varying lengths ( n ) of methylene groups of flexible spacers ( n = 3−12) were synthesized in our laboratory. Using POM we observed that all PSHQ n synthesized, with the exception of PSHQ3, have only a schlieren-textured nematic mesophase at temperatures between a glass transition temperature (or melting point) and the isotropization temperature; the nematic−isotropic transition temperature exhibits odd−even fluctuation with the number of methylene groups of the flexible spacer. We found that the isotropization enthalpy and isotropization entropy for PSHQ n do not follow a linear relationship with the number of methylene groups when the flexible spacer length becomes shorter than 7, which deviates from the findings for linear main-chain TLCPs reported in the literature. We ascribe this difference to the presence of bulky pendent arylsulfonyl side groups in the main-chain of PSHQ n . We found from both DSC and WAXD that (i) PSHQ n having odd numbers (5−11) of methylene groups exhibit a glassy nematic mesophase, while PSHQ3, having three methylene groups, has no liquid crystallinity, becoming an amorphous polymer with a glass transition temperature of 129 °C, and (ii) among the PSHQ n having even numbers (4−12) of methylene groups, PSHQ4 showed the highest degree of ordering in the crystalline structure. WAXD of PSHQ n melt-drawn fibers showed an odd−even fluctuation of chemical repeat unit d -spacing, very similar to that reported in the literature for linear main-chain TLCPs.
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Chang et al. (1997) studied this question.
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