Abstract
The structure of a side chain liquid crystalline poly(silylenemethylene) (-(SiCH3R-CH2)-: R = O(CH2)11O-Ph-Ph-CN, Ph = phenyl) (CN-11) has been studied by X-ray diffraction and differential scanning calorimetry (DSC). The DSC results showed that CN-11 has transitions at ∼92 °C (T2) and ∼147 °C (T1) during both cooling and immediate heating. A third transition occurred at ∼50 °C (T3) during heating after annealing at room temperature. The X-ray fiber pattern of the CN-11 annealed at room temperature showed several wide and small angle reflections which were indexed by a monoclinic unit cell with parameters a = 16.8 Å, b = 7.42 Å, c = 43.6 Å, and β = 102.1° (b: fiber direction), representing a crystal structure with layer thickness of ∼43 Å. Upon heating at T3, the crystal structure became less ordered (but somewhat more ordered than smectic A (SA) and smectic C (SC). This was followed by SA (or SC) phase at T2, and ultimately an isotropic state (I) at T1. The observed layer thickness (∼43 Å) is about ∼1.5 times the most extended side chain length, indicating a double-layer structure with tilted or interdigitated side chains. The X-ray fiber pattern had a four-point pattern at d = 4.52 Å, suggesting that the side chains in the crystal are likely to be tilted by 56° from the polymer fiber axis.
Original language | English |
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Pages (from-to) | 5169-5174 |
Number of pages | 6 |
Journal | Polymer |
Volume | 43 |
Issue number | 19 |
DOIs | |
State | Published - 2 Aug 2002 |
Keywords
- Hybrid polymers
- Poly(silylenemethylene)
- X-ray diffraction