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Two series of C2-substituted dimers carrying a central C2-hexyl- or C2-nonafluorohexyl malonate and two cyanobiphenyls attached via alkoxy spacers of various lengths (n = 6–12) were synthesised, and the mesomorphic properties were studied by differential scanning calorimetry, polarising optical microscopyand X-ray diffraction (wide-angle and small-angle X-ray scattering). The C2-substituent dimers together with the spacer lengths had a pronounced influence on the phase behaviour. In case of C2-hexyl-substituted dimers, shorter spacers favoured N phases (n = 6–9), while longer spacers favoured SmA phases (n ≥ 9). In addition, decreased clearing temperatures were observed. In contrast, C2-nonafluorohexyl-substituted dimers suppressed N phases and displayed only SmA phases. Moreover, clearing temperatures and phase stabilities considerably increased. Based on the experimentally determined layer thickness, a packing model for the SmA phases was proposed, where C2-substituted dimers displaced mesophases with molecules in a Y-conformation. As a result, less stable mesophases for C2-hexyl-substituted dimers due to weakened intermolecular interactions and more stable mesophases for C2-nonafluorohexyl-substituted dimers due to the fluorophobic effect and nanosegregation were obtained.

Mesomorphic properties of cyanobiphenyl dimers with a substituted central malonate unit: overruling effect of fluorination