Study of stacking interactions between two neutral tetra­thia­fulvalene molecules in Cambridge Structural Database crystal structures and by quantum chemical calculations

Tetra­thia­fulvalene (TTF) and its derivatives are very well known as electron donors with widespread use in the field of organic conductors and superconductors. Stacking interactions between two neutral TTF fragments were studied by analysing data from Cambridge Structural Database crystal structures and by quantum chemical calculations. Analysis of the contacts found in crystal structures shows high occurrence of parallel displaced orientations of TTF molecules. In the majority of the contacts, two TTF molecules are displaced along their longer C₂ axis. The most frequent geometry has the strongest TTF–TTF stacking interaction, with CCSD(T)/CBS energy of −9.96 kcal mol⁻¹. All the other frequent geometries in crystal structures are similar to geometries of the minima on the calculated potential energy surface.