Pressure-tuning Raman and infrared spectra of N-thiocyanato[tris(o-tolyl)]tin(IV), (o-CH3C6H4)3SnNCS

The effect of high external pressures on the Raman and IR spectra of the title compound (I) has been examined at ambient temperature. A pressure-induced phase transition was observed at 13–16 kbar, which is most likely second-order, resulting from slight rotations of the phenyl rings and/or the CH3 groups under the influence of pressure. No new peaks were observed in the spectra with increasing pressure indicating that no pressure-induced linkage isomerism or SnNCS⋯Sn bridging took place. The average pressure sensitivity (dν/dP) of the Raman-active vibrational modes is lower in the low-pressure region (0.23 cm−1/kbar) than in the high-pressure one (0.47 cm−1/kbar). In general, the IR-active modes are less sensitive to increasing pressure than are the Raman-active modes and the average dν/dP value for the IR-active modes in the low-pressure region is quite similar to that in the high-pressure region, i.e., about 0.23 cm−1/kbar.