Structural transformations and stability of benzo[ a ]pyrene under high pressure

Benzo[ a ]pyrene (B a P), C ₂₀ H ₁₂ , is a representative of polycyclic aromatic hydrocarbons (PAHs), which are ubiquitous in nature and the universe, where they are subjected to extreme conditions. This paper reports the results of investigations of the high-pressure behavior of B a P up to 28 GPa using in situ synchrotron single-crystal X-ray diffraction. We identified two previously unknown polymorphs, B a P-II ( P 2 ₁ / c ) at 4.8 GPa and B a P-III ( P 1 ) at 7.1 GPa. The structural transformation from B a P-I ( P 2 ₁ / c ) to B a P-II ( P 2 ₁ / c ) manifests as an abrupt change in the intermolecular angle and the unit-cell parameters a and b , whereas the transformation from B a P-II ( P 2 ₁ / c ) to B a P-III ( P 1 ) is characterized by a decrease in symmetry. According to density functional theory calculations, B a P-III is the most stable phase above 3.5 GPa. These studies advance our understanding of the structural dynamics and stability of PAHs under high pressure.