Issue 3, 2015

Tolane-based bent bolaamphiphiles forming liquid crystalline hexagonal honeycombs with trigonal symmetry

Abstract

Bolaamphiphiles consisting of a bent 1,3-bis(phenylethynyl)benzene core with two terminal glycerol units, a lateral n-alkyl chain in the bay-position and a methyl group at the apex of the central 1,3-substituted benzene ring have been synthesized via Sonogashira coupling reactions as key steps. The thermotropic and solvent-modified or solvent-induced liquid crystalline (LC) phases of these compounds were investigated by POM, DSC and X-ray scattering. Compounds with medium alkyl chain length form a hexagonal honeycomb LC phase with non-centrosymmetric trigonal p3m1 symmetry as a monotropic LC phase. The addition of water increases the LC phase range, leading to enantiotropic p3m1 phases and induces LC phases for the non-mesomorphic compounds with shorter and longer lateral alkyl chains.

Graphical abstract: Tolane-based bent bolaamphiphiles forming liquid crystalline hexagonal honeycombs with trigonal symmetry

Supplementary files

Article information

Article type
Paper
Submitted
21 Oct 2014
Accepted
06 Jan 2015
First published
07 Jan 2015
This article is Open Access
Creative Commons BY-NC license

New J. Chem., 2015,39, 2060-2066

Author version available

Tolane-based bent bolaamphiphiles forming liquid crystalline hexagonal honeycombs with trigonal symmetry

H. Gao, H. Cheng, Q. Liu, Y. Xiao, M. Prehm, X. Cheng and C. Tschierske, New J. Chem., 2015, 39, 2060 DOI: 10.1039/C4NJ01855A

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