Issue 31, 2016

Directed peptide amphiphile assembly using aqueous liquid crystal templates in magnetic fields

Abstract

An alignment technique based on the combination of magnetic fields and a liquid crystal (LC) template uses the advantages of both approaches: the magnetic fields offer non-contact methods that apply to all sample sizes and shapes, whilst the LC templates offer high susceptibilities. The combination introduces a route to control the spatial organization of materials with low intrinsic susceptibilities. We demonstrate that we can unidirectionally align one such material, peptide amphiphiles in water, on a centimeter scale at a tenfold lower magnetic field by using a lyotropic chromonic liquid crystal as a template. We can transform the aligned supramolecular assemblies into optically active π-conjugated polymers after photopolymerization. Lastly, by reducing the magnetic field strength needed for addressing these assemblies, we are able to create more complex structures by initiating self-assembly of our supramolecular materials under competing alignment forces between the magnetically induced alignment of the assemblies (with a positive diamagnetic anisotropy) and the elastic force dominated alignment of the template (with a negative diamagnetic anisotropy), which is directed orthogonally. Although the approach is still in its infancy and many critical parameters need optimization, we believe that it is a very promising technique to create tailor-made complex structures of (aqueous) functional soft matter.

Graphical abstract: Directed peptide amphiphile assembly using aqueous liquid crystal templates in magnetic fields

Supplementary files

Article information

Article type
Paper
Submitted
16 Mar 2016
Accepted
12 Jun 2016
First published
13 Jun 2016
This article is Open Access
Creative Commons BY-NC license

Soft Matter, 2016,12, 6518-6525

Author version available

Directed peptide amphiphile assembly using aqueous liquid crystal templates in magnetic fields

P. van der Asdonk, M. Keshavarz, P. C. M. Christianen and P. H. J. Kouwer, Soft Matter, 2016, 12, 6518 DOI: 10.1039/C6SM00652C

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