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Energy-level diagram showing the states involved in Raman spectra. Raman spectroscopy (/ ˈ r ɑː m ən /) (named after physicist C. V. Raman) is a spectroscopic technique typically used to determine vibrational modes of molecules, although rotational and other low-frequency modes of systems may also be observed. [1]
Furthermore, a vibration will be Raman active if there is a change in the polarizability of the molecule and if it has the same symmetry as one of the direct products of the x, y, z coordinates. To determine which modes are Raman active, the irreducible representation corresponding to xy, xz, yz, x 2 , y 2 , and z 2 are checked with the ...
Raman spectroscopy is used to analyze a wide range of materials, including gases, liquids, and solids. Highly complex materials such as biological organisms and human tissue [26] can also be analyzed by Raman spectroscopy. For solid materials, Raman scattering is used as a tool to detect high-frequency phonon and magnon excitations.
It states that no normal modes can be both Infrared and Raman active in a molecule that possesses a center of symmetry. This is a powerful application of group theory to vibrational spectroscopy, and allows one to easily detect the presence of this symmetry element by comparison of the IR and Raman spectra generated by the same molecule. [1]
In Raman and infrared spectroscopy, the selection rules predict certain vibrational modes to have zero intensities in the Raman and/or the IR. [11] Displacements from the ideal structure can result in relaxation of the selection rules and appearance of these unexpected phonon modes in the spectra.
A molecular vibration is a periodic motion of the atoms of a molecule relative to each other, such that the center of mass of the molecule remains unchanged. The typical vibrational frequencies range from less than 10 13 Hz to approximately 10 14 Hz, corresponding to wavenumbers of approximately 300 to 3000 cm −1 and wavelengths of approximately 30 to 3 μm.
Rotational–vibrational spectroscopy is a branch of molecular spectroscopy that is concerned with infrared and Raman spectra of molecules in the gas phase. Transitions involving changes in both vibrational and rotational states can be abbreviated as rovibrational (or ro-vibrational ) transitions.
The value of the depolarization ratio of a Raman band depends on the symmetry of the molecule and the normal vibrational mode, in other words, the point group of the molecule and its irreducible representation to which the normal mode belongs. Under Placzek's polarizability approximation, it is known that the depolarization ratio of a totally ...