Synthon preference in the cocrystal of 3,4,5-trifluorophenylboronic acid with urea

Abstract

The comprehensive description of the crystal structure of a novel 1:1 cocrystal of 3,4,5-trifluorophenylboronic acid with urea, C₆H₄BF₃O₂·CH₄N₂O, is presented. Both components are good candidates for crystal engineering as they can create a variety of supramolecular synthons. The preference for the formation of different hetrosynthons is verified based on theoretical calculations. The syn–anti conformation of boronic acid has been found to be the most favourable in the formation of intermolecular interactions with urea. Moreover, the distortions present in the boron coordination sphere have been described quantitatively based on experimental data according to bond-valence vector model calculations. The results revealed that the deformation of the sphere is typical for a syn–anti conformation of boronic acids. The supramolecular structure of the cocrystal is composed of large synthons in the form of layers made up of O—H...O and N—H...O hydrogen bonds. The layers are joined via N—H...F hydrogen bonds which are unusual for urea cocrystal structures.