Lyomesophases of C3-symmetrical bipyridine-based discs in alkanes: an X-ray diffraction study

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DOI http://dx.doi.org/10.1021/la9003017
Reference R. Martín-Rapún, D. Byelov, A.R.A. Palmans, W.H. de Jeu and E.W. Meijer, Lyomesophases of C3-symmetrical bipyridine-based discs in alkanes: an X-ray diffraction study, Langmuir 25, (15), 8794-8801 (2009)

The importance of the role of alkane solvents in the self-assembly process of π-conjugated molecules is well recognized but hardly understood. Here we present our results on the X-ray diffraction studies that we conducted to gain insight into the supramolecular structure of mixtures of a bipyridine-based molecule (1) with alkanes. Independent of the alkane used (linear or branched), above xw > 0.06 (with xw being the weight fraction of 1) the mixtures show lyotropic liquid-crystalline behavior. The nature of the lyomesophase depends only on xw and not on the nature of the alkane (linear or branched). A columnar rectangular phase is present when xw > 0.66. Upon dilution of 1, a columnar hexagonal phase is assigned first (0.50 < xw < 0.65), and finally a columnar nematic phase is observed when xw < 0.50. Concentration-dependent SAXD measurements revealed that the dilution of 1 can be viewed as a swelling process. First, solvent molecules occupy space between the columns formed by 1, which are not disrupted. This process can quantitatively be described by a 2D swelling model. Only at lower concentrations does 3D swelling start as the columns start breaking into shorter fragments.