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Abstract
Non-symmetric dimesogens are composed of two different mesogenic units linked via a flexible spacer. In this study, a new type of non-symmetric dimesogen has been built through the self-assembly via intermolecular hydrogen bonding between appropriately designed H-bond donor (3-cholesteryloxycarbonylpentanoic acid) and acceptor (aromatic mesogen with a pyridyl group) moieties. As for covalently linked dimesogens, several types of smectic periodicities are observed for these H-bonded cholesteryl compounds depending on the length of the terminal chain of the acceptor moiety: a smectic periodicity resulting from associated dimesogens is observed for long terminal chains, while short chain homologues display an intercalated structure corresponding to half the molecular length. The competition between these two incommensurate lengths can induce an incommensurate smectic phase where the two smectic periodicities coexist at long range.
