Topochemical, Single-Crystal-to-Single-Crystal [2+2] Photocycloadditions Driven by Chalcogen-Bonding Interactions.

Abstract

The face‐to‐face association of (E)‐1,2‐di(4‐pyridyl)ethylene (bpen) molecules into rectangular motifs stabilized for the first time by chalcogen bonding (ChB) interactions is shown to provide photoreactive systems leading to cyclobutane formation through single‐crystal‐to‐single‐crystal [2+2] photodimerizations. The chelating chalcogen bond donors are based on original aromatic, ortho‐substituted bis(selenocyanato)benzene derivatives 1–3, prepared from ortho‐diboronic acid bis(pinacol) ester precursors and SeO2 and malononitrile in 75–90 % yield. The very short intramolecular Se⋅⋅⋅Se distance in 1–3 (3.22–3.24 Å), a consequence of a strong intramolecular ChB interaction, expands to 3.52–3.54 Å in the chalcogen‐bonded adducts with bpen, a distance (<4 Å) well adapted to the face‐to‐face association of the bpen molecules into the reactive position toward photochemical dimerization.