The crystal structure of hexaphenylbenzene under high hydrostatic pressure

Abstract

High-pressure single-crystal X-ray diffraction, intermolecular interaction energy calculations, and density functional theory are used to examine the structure and emission properties of the classical organic rotor hexaphenylbenzene (C₆Ph₆) during hydrostatic compression to 4.14 GPa. Under applied pressure, the inter-phenyl distance in intermolecular dimers with displaced-stacked conformations gradually shortens, indicating the likelihood for hexaphenylbenzene to undergo mechanofluorochromism, while the stability of the crystal is governed by T-shaped intermolecular phenyl dimers. The theoretical band gaps and UV absorption spectra of hexaphenylbenzene at ambient pressure and 1.05 GPa predict an absorption red-shift by about 50 nm, in agreement with shortening of the intermolecular displaced-stacked interactions in the crystal under pressure. Compression of the intermolecular interactions in hexaphenylbenzene prompts a non-centrosymmetric to centrosymmetric phase transition from orthorhombic Pna2₁ to monoclinic P2₁/c at 1.05 GPa, as the approximately hexagonally-packed layers of hexaphenylbenzene molecules adopt a perfect hexagonal arrangement. This pressure-stimulated phase transition involving gain of centrosymmetry is an interesting structural phenomenon that is previously unreported in organic crystals.