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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]
Raman spectroscopy employs the Raman effect for substances analysis. The spectrum of the Raman-scattered light depends on the molecular constituents present and their state, allowing the spectrum to be used for material identification and analysis. Raman spectroscopy is used to analyze a wide range of materials, including gases, liquids, and ...
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 ...
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.
In CO 2, the bending vibration ν 2 (667 cm −1) has symmetry Π u.The first excited state of ν 2 is denoted 01 1 0 (no excitation in the ν 1 mode (symmetric stretch), one quantum of excitation in the ν 2 bending mode with angular momentum about the molecular axis equal to ±1, no excitation in the ν 3 mode (asymmetric stretch)) and clearly transforms according to the irreducible ...
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.
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]