Abstract
We report, to the best of our knowledge, for the first time the vibrational, IR and Raman, spectra of 12-thiacrown-4 (12t4) and 18-thiacrown-6 (18t6). To predict in what conformation 12t4 and 18t6 exist, for the vibrational analysis of both molecules and to assess the performance of the different computational methods for the accurate prediction of the vibrational frequencies of relatively large molecules, the computations were done using the harmonic and anharmonic force fields using the 6-31G* and 6-311G** basis sets. The computations were performed at the HF, B3LYP, CAM-B3LYP, BLYP, BP86, G96LYP, PBE1PBE, TPSSH and MP2 levels. Comparison was made between the calculated and experimental vibrational frequencies as indicated by the root-mean-square (rms) deviations, using either the unscaled and scaled harmonic vibrational frequencies and, unscaled, anharmonic vibrational frequencies. For the harmonic vibrational frequencies two scaling schemes were used. One uses one-scale-factor (1SF) scaling and the other uses 8SF scaling. In terms of the vibrational analysis of 12t4 and 18t6, the report confirms the solid state X-ray structure of D-4 of 12t4 and C-2 of 18t6. It is concluded that a lower rms deviation is obtained using 1SF scaled harmonic vibrational frequencies at even the HF/6-31G* level than using anharmonic vibrational frequencies at the MP2/6-311G** level. The CAM-B3LYP method showed some improvement over the traditional B3LYP method. (C) 2013 Elsevier B.V. All rights reserved.