Issue 46, 2008

Photochromic glassy liquid crystals comprising mesogenic pendants to dithienylethene cores

Abstract

Photochromic glassy liquid crystals were synthesized using dithienylethenes as the volume-excluding cores to which liquid crystalline mesogens were chemically bonded through alkyl spacers. Nematic, smectic, and cholesteric glassy liquid crystals were demonstrated with glass transition temperatures above 90 °C and clearing points up to 220 °C without traces of crystallization on cooling or crystalline melting on heating. A monodomain cholesteric glassy liquid crystalline film containing an enantiomeric 2-methylpropylene chiral spacer was characterized as a left-handed helical stack, exhibiting a selective reflection band centered at 686 nm, an orientational order parameter of 0.65 for the quasi-nematic layers, and a combination of reflective coloration with photoswitchable absorptive coloration.

Graphical abstract: Photochromic glassy liquid crystals comprising mesogenic pendants to dithienylethene cores

Supplementary files

Article information

Article type
Paper
Submitted
27 Jun 2008
Accepted
10 Sep 2008
First published
22 Oct 2008

J. Mater. Chem., 2008,18, 5592-5598

Photochromic glassy liquid crystals comprising mesogenic pendants to dithienylethene cores

C. Kim, K. L. Marshall, J. U. Wallace and S. H. Chen, J. Mater. Chem., 2008, 18, 5592 DOI: 10.1039/B810955A

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