Issue 38, 2006

Supramolecular chirality of columnar mesophases consisting of H-bonded complexes of melamine and polycatenar benzoic acids

Abstract

The present work describes a series of H-bonded complexes consisting of a melamine derivative and polycatenar acids that show columnar liquid crystalline behaviour. Chirality has been transferred from the molecular blocks (either the acids, A3* and A4*, or the melamine, T2*) to the columnar organization. Particular effort and attention has been paid to structural characterization by NMR techniques [1D NMR spectroscopy and diffusion-ordered spectroscopy (DOSY) experiments] of the complexes in solution. The mesomorphic arrangements of all the complexes have been studied by polarizing optical microscopy (POM), differential scanning microscopy (DSC) and powder X-ray diffraction. The chiral nature of the supramolecular organization in the mesophase has been confirmed by circular dichroism spectroscopy on neat samples over a range of temperatures.

Graphical abstract: Supramolecular chirality of columnar mesophases consisting of H-bonded complexes of melamine and polycatenar benzoic acids

Supplementary files

Article information

Article type
Paper
Submitted
07 Jun 2006
Accepted
01 Aug 2006
First published
25 Aug 2006

J. Mater. Chem., 2006,16, 3768-3773

Supramolecular chirality of columnar mesophases consisting of H-bonded complexes of melamine and polycatenar benzoic acids

L. Álvarez, J. Barberá, L. Puig, P. Romero, J. L. Serrano and T. Sierra, J. Mater. Chem., 2006, 16, 3768 DOI: 10.1039/B608066A

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