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Updated: May 16, 2025

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Published on: February 7, 2017
Supramolecular Organization in Monolayers of Pyrene-Functionalized Asymmetric Twist-Bend Nematic Dimers: Comparison
Agnieszka Maranda-Niedbała1, Tomasz Jaroch2, Rebecca Walker3
1Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, Warszawa 01-224, Poland.
Abstract:
Two-dimensional (2D) supramolecular organization of asymmetric liquid crystal dimers containing two chemically different mesogenic groups, namely, cyanobiphenyl and pyreneiminomethyl phenoxy groups, linked with an oligomethylene linker of different length (six or eight -CH2- units), was studied using scanning tunneling microscopy. For this purpose, monolayers of these dimers were deposited on an HOPG substrate from their solutions in hexane by drop-casting and imaged at nanometer resolution after drying. A detailed discussion of two possible different supramolecular organizations is presented. In the case of the first one, termed the "lamellar structure", the molecules in each layer are arranged in parallel molecular rows. Comparative analysis of the monolayer structure with already reported XRD data on 3D organization of the same molecules in a single crystal revealed significant differences resulting from (i) different ordering preferences in 2D and 3D systems and (ii) effects of the interactions of the deposited molecules with the graphite substrate. A small extension of the linker by two methylene groups does not change the type of ordering in the monolayer but causes an extension of the unit cell in one direction, indicating that the lamellar structure is stabilized by rows of densely packed large aromatic pyrene units. Studies of the derivative with a longer linker (containing eight -CH2- units) also showed the possibility of the occurrence of an alternative type of its monolayer organization, termed here "aggregate structure". In this case, the monolayer consists of ordered aggregates of two molecules. According to the authors' knowledge, this type of structural organization has not yet been reported for this family of compounds. It is, however, qualitatively consistent with the already described supramolecular ordering in CBO5O.Py (CCDC 2019485), a compound closely resembling the dimers studied in this research.
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