Lihua Cui

TL;DR: The solvent-induced chiral structural transition of a 2-hydroxy-7-pentadecyloxy-9-fluorenone (HPF) molecules' self-assembled adlayer through coassembly with achiral aliphatic solvents under different concentrations provides a simple and alternative strategy to construct the 2D chiral assembled monolayer.

TL;DR: In this article, a heterochiral double rosette-like structure was fabricated for the first time via hydrogen bond interactions with achiral 1-octanoic acid under low concentrations.

TL;DR: Insight is provided into the structural variety exhibited by a series of organic molecules and important guidelines to control the morphology by changing the solution concentration are furnished.

TL;DR: The results showed that there were tremendous solvent-dependent self-assemblies in 2D ordering for the surface-confined target molecules, and thermodynamic calculations indicated that the stable structural coexistence of the fluorenone derivative was attributed to synergistic intermolecular dipole-dipole and van der Waals forces at l/s interface.

TL;DR: In this paper, a two-dimensional hydrogen-bonded networks formed in the self-assembly of 1,3,5-tris(10-carboxydecyloxy) benzene (TCDB) showed regular solvent-and guest-induced supramolecular structural properties, which have been presented by scanning tunneling microscopy at the liquid-solid interface at ambient conditions.