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New 2,2′-Substituted 4,4′-Dimethoxy-6,6′-dimethyl[1,1′-biphenyls], Inducing a Strong Helical Twisting Power in Liquid Crystals

✍ Scribed by Richard Holzwarth; Richard Bartsch; Zoubair Cherkaoui; Guy Solladié


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
157 KB
Volume
10
Category
Article
ISSN
0947-6539

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✦ Synopsis


Abstract

Based on the stabilisation of the molecular motion by the chiral residue, novel optically active biphenylic chiral dopants for nematic liquid crystals were developed. This molecular congestion was obtained by introducing mesogenic residues on the 2,2′‐positions of the chiral biphenyl; this led to a novel molecular architecture that was found to be efficient. The synthesised optically active biphenyls were characterised with very short cholesteric pitches when used as chiral dopants in nematic liquid crystals. The synthesis of the enatiomerically pure biphenyl dopants and their preliminary physicochemical characterisations are described.


📜 SIMILAR VOLUMES


New 2,2'-Substituted 6,6'-Dimethylbiphen
✍ Richard Holzwarth; Richard Bartsch; Zoubair Cherkaoui; Guy Solladié 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 106 KB

## Abstract New optically active tetra‐__ortho__‐substituted biphenyl chiral dopants for nematic liquid crystals are described. It was shown, with respect to our previous results, that biphenyl chiral dopants bearing only mesogenic residues on their 2,2'‐positions and without any substituents on th