In this study, we prepared two series of new side-chain cholesteric liquid-crystalline elastomers (PI and PII) derived from the same chiral bisolefinic crosslinking units and different nematic liquid-crystalline monomers. The chemical structures of the monomers and polymers obtained were confirmed by Fourier transform infrared and 1H-NMR spectroscopy. The phase behavior properties were investigated by differential scanning calorimetry, thermogravimetric analysis, and polarizing optical microscopy. The effect of the length of the carbochain on the phase behavior of the elastomers was investigated. The polymers of the PI and PII series showed similar properties. Polymer P1 showed a nematic phase, P2–P7 showed a cholesteric phase, and P4–P7, with more than 6 mol % of the chiral crosslinking agent, exhibited a selective reflection of light. The elastomers containing less than 15 mol % of the crosslinking units displayed elasticity, a reversible phase transition with wide mesophase temperature ranges, and a high thermal stability. The experimental results demonstrate that the glass-transition temperatures first decreased and then increased; the isotropization temperatures and the mesophase temperature ranges decreased with increasing content of crosslinking agent. However, because of the different lengths of the carbochain, the glass-transition temperatures and phase-transition temperatures of the PI series were higher than those of the PII series, and the PI and PII elastomers had their own special optical properties. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1204–1210, 2005
If you can't find a tool you're looking for, please click the link at the top of the page to "Go to old article view". Alternatively, view our Knowledge Base articles for additional help. Your feedback is important to us, so please let us know if you have comments or ideas for improvement.