Diastereomeric Configuration Drives an On-Surface Specific Rearrangement into Low Bandgap Non-Benzenoid Graphene Nanoribbons.

Stereochemistry, usually associated with the three-dimensional arrangement of atoms in molecules, is crucial in processes like life functions, drug action, or molecular reactions. This three-dimensionality typically originates from sp hybridization in organic molecules, but it is also present in out-of-plane sp-based molecules as a consequence of helical structures, twisting processes, and/or the presence of nonbenzenoid rings, the latter significantly influencing their global stereochemistry and leading to the emergence of new exotic properties. In this sense, on-surface synthesis methodologies provide the perfect framework for the precise synthesis and characterization of organic systems at the atomic scale, allowing for the accurate assessment of the associated stereochemical effects. In this work, we demonstrate the importance of the initial diastereomeric configuration in the surface-induced skeletal rearrangement of a substituted cyclooctatetraene (COT) moiety-a historical landmark in the understanding of aromaticity-into a cyclopenta[,]azulene (CPA) one in a chevron-like graphene nanoribbon (GNR). These findings are evidenced by combining bond-resolved scanning tunneling microscopy with theoretical ab initio calculations. Interestingly, the major well-defined product, a CPA chevron-like GNR, exhibits the lowest bandgap reported to date for an all-carbon chevron-like GNR, as evidenced by scanning tunneling spectroscopy measurements. This work paves the way for the rational application of stereochemistry in the on-surface synthesis of novel graphene-based nanostructures.