Issue 4, 2013

Effect of lateral fluoro substituents of rodlike tolanecyano mesogens on blue phase temperature ranges

Abstract

Several kinds of tolane cyano derivatives with different lateral fluoro substituents are doped with chiral additives to induce the blue phase (BP). Fluoro substituents are found to exert a great effect on the BP ranges for biphenyl mesogens. The laterally difluorinated compounds exhibit wider BP ranges than their corresponding mono-fluorinated homologues when equal chiral dopant is added, while the non-fluorinated compounds show direct isotropic (Iso) to chiral nematic (N*) transitions, even in highly chiral systems. By adjusting the concentrations of the chiral dopant ISO(6OBA)2 in the fluorinated liquid crystals, the BP ranges can be broadened to more than 12 °C. Competition between the steric repulsions caused by the lateral fluoro substituents and π–π interactions of the aromatic cores is supposed to be the main factor that leads to the above results. Apart from this, a weak C–H⋯F interaction may have also been conducive to the BP stabilization.

Graphical abstract: Effect of lateral fluoro substituents of rodlike tolane cyano mesogens on blue phase temperature ranges

Supplementary files

Article information

Article type
Paper
Submitted
04 Aug 2012
Accepted
06 Nov 2012
First published
26 Nov 2012

Soft Matter, 2013,9, 1172-1177

Effect of lateral fluoro substituents of rodlike tolane cyano mesogens on blue phase temperature ranges

B. Li, W. He, L. Wang, X. Xiao and H. Yang, Soft Matter, 2013, 9, 1172 DOI: 10.1039/C2SM26807H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements