Abstract
Bis [(ω-(4′-cyanobiphenyl)-4-yl)oxy-n-alkyl]norborn-5-ene-2,3-dicarboxylate was polymerised via ring opening metathesis polymerisation (ROMP). Two disubstituted polynorbornene derivatives both of cis configuration with different length of the side-chain were studied. Differential scanning calorimetry (DSC) was used to study the effect of thermal history on the assignment of the glass transition event associated with the biaxial orientation of a smectic phase. Glass transition temperatures, the change of isobaric specific heats at Tg and the enthalpies of isotropisation were calculated. The DSC traces only show the classic step-wise change in Tg in some cases, giving the evidence that the amorphous domains are constrained and highly restricted in movement due to the morphology developed as a result of the biaxial stretching. Based on the literature data of mono- and disubstituted polynorbornene derivatives and our calorimetric experiments, the shape of Tg dependence on number of (CH2) units is interpreted. The origin of this shape is discussed.
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Danch, A., Lohner, K., Ungerank, M. et al. Thermal Analysis of the Conformational Disorder in SCLC Polymers with Rigid Backbone Glass transition studies. Journal of Thermal Analysis and Calorimetry 54, 161–170 (1998). https://doi.org/10.1023/A:1010177121068
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DOI: https://doi.org/10.1023/A:1010177121068