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Invited Articles

Thermotropic and lyotropic liquid crystalline phases of Guerbet branched-chain -D-glucosides

, , , , , , , & show all
Pages 1725-1734 | Received 12 Jul 2011, Accepted 15 Sep 2011, Published online: 17 Oct 2011
 

Abstract

The effect of chain branching on glycolipid thermotropic and lyotropic phases was investigated for a series of synthetic β-D-glucosides derived from Guerbet alcohols, whose total hydrocarbon chain length ranged from C8 to C24. The compounds, which can be viewed as isosteric mimics for glycoglycerolipids, were synthesised in high purity and their liquid crystalline phases were studied using optical polarising microscopy (OPM), and small-angle X-ray diffraction. When dry, the shortest compound (total C8) exhibits a monotropic Lα phase while longer ones (C16 and C20) adopt inverse hexagonal HII phases. The C24 compound forms an ordered lamellar phase at room temperature, but exhibits a metastable HII phase upon cooling. Curiously the intermediate chain length homologue (C12) adopts an isotropic inverse micellar (L2) phase in the dry state over the range of temperatures studied. Upon hydration, the C8 compound dissolves, and the C12 compound forms a fluid lamellar Lα phase. The C16 Guerbet glucoside (i.e. β-Glc-C10C6) exhibits an inverse bicontinuous cubic phase of space group Ia3d in excess water, never previously observed in branched-chain lipids, and very seldom observed in excess water. The C20 compound remains in the HII phase upon hydrating, with the lattice parameter swelling substantially.

Acknowledgements

This work was supported by Malaysian grants UM/MOHE HIR and UM.C/625/1/HIR/MOHE/05, and by EPSRC (UK) Platform grant EP/G00465X. We thank Diamond Light Source (UK) and the Australian Synchrotron for synchrotron beamtime.

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