Evaluation of fluorine-mediated intermolecular interactions in tetratluorinated tetrahydroisoquinohne derivatives: synthesis and computational studies

Intermolecular interactions involving the aromatic C-F group in the absence of other strong hydrogen bond acceptors is the theme of this article. Weak interactions involving fluorine are known to generate various supramolecular synthons, thereby altering the crystal structures of small organic molecules. It is demonstrated that the weak interactions involving organic fluorine play a major role in directing crystal packing of highly flexible organic molecules like diphenyl tetrahydroisoquinolines reported herein. The intramolecular C-H center dot center dot center dot F hydrogen bonds are found to be significant in controlling the molecular conformation in specific cases wheras the intermolecular interactions involving the C-F groups result in a wide range of supramolecular synthons involving C-H center dot center dot center dot F and C-F center dot center dot center dot F-C interactions. The interactions are studied computationally to provide insight into their energies and the topology of the interactions is studied using Atoms in Molecules. C-H center dot center dot center dot F-C interactions are found to be quite stabilizing in nature with the stabilization energy of -13.9 kcal mol(-1).