Chiral symmetry breaking in soft matter is a hot topic of current research. Recently, such a phenomenon was found in a fluidic phase showing orientational order of molecules—the nematic phase; although built of achiral molecules, the phase can exhibit structural chirality—average molecular direction follows a short-pitch helix. Here, we report a series of achiral asymmetric dimers with an odd number of atoms in the spacer, which form twisted structures in nematic as well as in lamellar phases. The tight pitch heliconical nematic (NTB) phase and heliconical tilted smectic C (SmCTB) phase are formed. The formation of a variety of helical structures is accompanied by a gradual freezing of molecular rotation. In the lowest temperature smectic phase, HexI, the twist is expressed through the formation of hierarchical structure: nanoscale helices and mesoscopic helical filaments. The short-pitch helical structure in the smectic phases is confirmed by resonant X-ray measurements.

We experimentally demonstrate fast flexoelectrooptic switching in a liquid crystal cell containing bimesogendoped and polymer-stabilized cholesteric. The device exhibits a response time of less than 0.7 ms and with low hysteresis and color dispersion which is suitable for potential applicationsincluding field-sequential color displays. .

In this review we consider the relationships between molecular structure and the tendency of liquid crystal dimers to exhibit smectic phases, and show how our application of these led to the recent discovery of the twist-bend, heliconical smectic phases. Liquid crystal dimers consist of molecules containing two mesogenic groups linked through a flexible spacer, and even- and odd-membered dimers differ in terms of their average molecular shapes. The former tend to be linear whereas the latter are bent, and this difference in shape drives very different smectic behaviour. For symmetric dimers, in which the two mesogenic groups are identical, smectic phase formation may be understood in terms of a microphase separation into distinct sublayers consisting of terminal chains, mesogenic units and spacers, and monolayer smectic phases are observed. By contrast, intercalated smectic phases were discovered for nonsymmetric dimers in which the two mesogenic units differ. In these phases, the ratio of the layer spacing to the molecular length is typically around 0.5 indicating that unlike segments of the molecules overlap. The formation of intercalated phases is driven by a favourable interaction between the different liquid crystal groups. If an odd-membered dimer possesses sufficient molecular curvature, then the twist-bend nematic phase may be seen in which spontaneous chirality is observed for a system consisting of achiral molecules. Combining the empirical relationships developed for smectogenic dimers, and more recently for twist-bend nematogenic dimers, we show how dimers were designed to show the new twist-bend, heliconical smectic phases. These have been designated SmCTB phases in which the director is tilted with respect to the layer plane, and the tilt direction describes a helix on passing between layers. We describe three variants of the SmCTB phase, and in each the origin of the symmetry breaking is attributed to the anomalously low-bend elastic constant arising from the bent molecular structures.

Non‐symmetric lactate‐based chiral liquid crystal dimers containing an odd‐membered spacer are shown to exhibit a chiral twist‐bend nematic phase which is stable on cooling to room temperature. A comparison of racemic and optically pure materials reveals that the pitch length in the N*TB phase is not influenced by molecular chirality, whereas the nematic‐twist‐bend nematic transition temperature is increased.

Das Schicksal intermediärer π‐Radikale ist entscheidend bei der Bu3SnH‐vermittelten Cyclisierung durch radikalische aromatische Substitution. So lagert sich die Bromverbindung 1 über das Radikal 2 in das Oxindol 3 um (AIBN=Azobisisobutyronitril). Dabei ist die Abspaltung des H‐Atoms von der π‐radikalischen Zwischenstufe durch den Radikalstarter ein wichtiger Schritt im Mechanismus. Die Ergebnisse zeigen, dass aromatische Lösungsmittel nicht immer das Solvens der Wahl für Radikalreaktionen sind.