Group theory is an important component for understanding the fundamentals of vibrational spectroscopy. The molecular or solid state symmetry of a material in conjunction with group theory form the basis of the selection rules for infrared absorption and Raman scattering. Here we investigate, in a two-part series, the application of group theory for practical use in laboratory vibrational spectroscopy.
In part I of this two-part series we present salient and beneficial aspects of group theory applied to vibrational spectroscopy in general and Raman spectroscopy in particular. We highlight those aspects of molecular symmetry and group theory that will allow readers to beneficially apply group theory and polarization selection rules in both data acquisition and interpretation of Raman spectra. Small-molecule examples are presented that show the correlation between depictions of normal vibrational modes and the mathematical descriptions of group theory.
Why Would I Want to Use Group Theory?Many of us learned group theory in undergraduate or graduate school. For some, the last time that they used or understood group theory was in preparation for a final exam. Furthermore, the application of group theory to anything other than the small molecules covered in textbooks can seem like an ordeal in tedious mathematics and bookkeeping. But, it doesn't have to be that way. So, let's brush up on those aspects of group theory that apply to vibrational spectroscopy, and you'll soon find that there is a lot more information to be gained through the application of group theory and Raman polarization selection rules in both data acquisition and interpretation of the spectra.
There are so many good instructional and reference materials in books (1–11) and articles (12–15) on group theory that there did not seem to be any good reason to attempt to duplicate that work in this installment. Rather, I would like to summarize and present the most salient and beneficial aspects of group theory when it is applied to vibrational spectroscopy in general and Raman spectroscopy in particular.
And speaking of being allowed, it is important to note that not all vibrational modes of a molecule are spectroscopically active. The complete set of normal vibrational modes of a molecule will belong to one of the following three categories: Raman active, infrared active, or silent. Here is where the last two columns of the character table become particularly helpful to the spectroscopist. The next to last column indicates the axes along which a change in the dipole moment will occur with molecular vibration and thereby allow that vibration to be infrared (IR) active (that is, will absorb IR radiation at the frequency of the changing dipole moment). Only the A 1, B 1, or B 2 species of normal vibrational modes of a molecule in this C 2v point group will be IR active. Likewise, all four symmetry species may be Raman active. The last column indicates the axes along which a change in polarizability will occur with molecular vibration and thereby allow that vibration to be Raman active (that is, will scatter radiation at the frequency of the vibrational modulation of the polarizability). One final point here is that any Raman bands belonging to the totally symmetric A 1 (or A g) symmetry species will be polarized; that is, allowed and observed with the Raman analyzer in a configuration parallel to the incident polarization, but absent or weak when the analyzer is configured perpendicular to the incident polarization. We will have more to say on the practical application of the Raman polarization selection rules in the second installment of this two-part series.