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Issue 37, 2015
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Chirality amplification and detection by tactoids of lyotropic chromonic liquid crystals

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Abstract

Detection of chiral molecules requires amplification of chirality to measurable levels. Typically, amplification mechanisms are considered at the microscopic scales of individual molecules and their aggregates. Here we demonstrate chirality amplification and visualization of structural handedness in water solutions of organic molecules that extends over the scale of many micrometers. The mechanism is rooted in the long-range elastic nature of orientational order in lyotropic chromonic liquid crystals (LCLCs) formed in water solutions of achiral disc-like molecules. The nematic LCLC coexists with its isotropic counterpart, forming elongated tactoids; the spatial confinement causes a structural twist even when the material is nonchiral. Minute quantities of chiral molecules such as the amino acid L-alanine and limonene transform the racemic array of left- and right-twisted tactoids into a homochiral set. The left and right chiral enantiomers are readily distinguished from each other as the induced structural handedness is visualized through a simple polarizing microscope observation. The effect is important for developing our understanding of chirality amplification mechanisms; it also might open up new possibilities in biosensing.

Graphical abstract: Chirality amplification and detection by tactoids of lyotropic chromonic liquid crystals

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Publication details

The article was received on 02 Jul 2015, accepted on 22 Jul 2015 and first published on 22 Jul 2015


Article type: Paper
DOI: 10.1039/C5SM01632K
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Soft Matter, 2015,11, 7257-7263

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    Chirality amplification and detection by tactoids of lyotropic chromonic liquid crystals

    C. Peng and O. D. Lavrentovich, Soft Matter, 2015, 11, 7257
    DOI: 10.1039/C5SM01632K

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