Oxiranes bearing a 4-cyanobiphenyl-4'-oxy mesogenic group with spacers of different length have been synthesized from glycidyl p-toluenesulfonate or epichlorohydrin (racemic or optically active). These monomers were polymerized with anionic initiators (CsOH, tBuOK (a))) or a chelate initiator (A1Et(3)/H2O/acetylacetone (a))). A transfer of chirality from the polymer backbone to the mesophase is observed for polyethers with a short spacer. A cholesteric phase is observed for the optically active polymer while the racemic polymer is nematic. Increasing the length of the spacer leads to a smectic mesophase. However, in that case, the effect of the chiral centre of the polymer backbone on the mesomorphous properties is not detected.
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页码:2941 / 2954
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WULFF G, 1994, ANGEW CHEM INT EDIT, V33, P188, DOI 10.1002/anie.199401881