Rotation in an Enantiospecific Self-Assembled Array of Molecular Raffle Wheels

Tailored nano-spaces can control enantioselective adsorption and molecular motion. We report on the spontaneous assembly of a dynamic system-a rigid kagome network with each pore occupied by a guest molecule-employing solely 2,6-bis(1H-pyrazol-1-yl)pyridine-4-carboxylic acid on Ag(111). The network cavity snugly hosts the chemically modified guest, bestows enantiomorphic adsorption and allows selective rotational motions. Temperature-dependent scanning tunnelling microscopy studies revealed distinct anchoring orientations of the guest unit switching with a 0.95 eV thermal barrier. H-bonding between the guest and the host transiently stabilises the rotating guest, as the flapper on a raffle wheel. Density functional theory investigations unravel the detailed molecular pirouette of the guest and how the energy landscape is determined by H-bond formation and breakage. The origin of the guest's enantiodirected, dynamic anchoring lies in the specific interplay of the kagome network and the silver surface.

Automated summary

Tailored nano-spaces can control enantioselective adsorption and molecular motion through the spontaneous assembly of a dynamic system on Ag(111) using 2,6-bis(1H-pyrazol-1-yl)pyridine-4-carboxylic acid. The network cavity snugly hosts the chemically modified guest, bestows enantiomorphic adsorption, and allows selective rotational motions. Hydrogen bonding plays a crucial role in stabilizing the rotating guest and influencing the energy landscape formation.