Pressure induced transformations in sorbic acid.

This research reports a pressure dependent Raman study of the sorbic acid between 0.0 and 10.0GPa. The unpolarized Raman spectra were measured in the spectral range of 20–3000cm−1. The high-pressure Raman scattering study of the sorbic acid showed that it underwent a gradual, disordering process. At the room temperature and at the ambient pressure conditions, the crystal structure of the sorbic acid belongs to the monoclinic system with a C2/c (C2h6) space group. The pressure increase induced a higher disorder in the monoclinic unit cell, since a single bending mode, and only very broad stretching Raman modes are present at pressure of ~10GPa. Upon pressure release the high-pressure phase transforms directly into the ambient-pressure phase. The presence of the internal vibrational modes is a guarantee that the molecular structure is maintained. Beyond this, the presence of external modes shows that the crystal has a memory to reverse the process and suggest that the crystal, which was in high disorder (broad Raman bands), does not suffer decomposition in the crystalline structure. The DFT calculations for the sorbic acid were performed in order to understand the vibrational properties. The theoretical study showed that the volume of the unit cell and beta angle decrease significatively when passing from the 0.0GPa to 8.0GPa. The decreases in the volume and beta angle of this particular unit cell were supposed to induce the larger increase in the bandwidths of the observed bands, pointing to some disorder in the monoclinic phase.