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Miscellany

Optical and electro‐optical properties of bimesogenic organosiloxane antiferroelectric liquid crystals with molecular tilt approaching 45 degrees

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Pages 173-181 | Received 13 Jul 2004, Accepted 22 Sep 2004, Published online: 20 Feb 2007
 

Abstract

We have studied the optical and electro‐optical properties of three different bimesogenic siloxane materials. The dimers are symmetrical and the two mesogenic groups are connected by a siloxane unit containing three Si atoms and methylene spacers. The mesogens contain F, Cl and Br substituents, respectively, laterally attached to the phenyl ring lying closest to the chiral centre of the mesogen. These materials each exhibited a broad temperature range antiferroelectric phase and large molecular tilt, which is almost temperature‐independent. We have shown that, at low temperatures, the molecular tilt in the antiferroelectric phase is the same as the apparent molecular tilt in the field‐induced ferroelectric state and is close to 45°. It was found that the antiferroelectric phase of these compounds, aligned in such way that the dimeric molecules were lying in a plane parallel to the confining substrates, exhibited very low in‐plane birefringence. For this reason, samples of the compounds inserted between crossed polarizers in the antiferroelectric state exhibited an extremely dark state, with contrast ratios as high as 1000:1, which did not change noticeably on rotating the sample between the crossed polarizers. It was shown that the optically isotropic siloxane moiety did not contribute to the optical properties, viz. birefringence or tilt angle, but served to enhance the promotion of the antiferroelectric phase and the temperature independent properties. We also showed the existence of a linear electro‐optic response in the pretransitional region of the antiferroelectric phase of these compounds over a moderate range of fields.

Acknowledgements

H.J.C. thanks the EPSRC for support of this research through two grants GR/N30972 and GR/N22250 for materials research.

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