Raman optical activity
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Raman optical activity (ROA) is a vibrational spectroscopic technique that is reliant on the difference in intensity of Raman scattered right and left circularly polarised light due to molecular chirality.
History of Raman optical activity
The field began with the doctoral work of Laurence D. Barron with Peter Atkins at the University of Oxford and was later further developed by Barron with David Buckingham at the University of Cambridge.
More developments, including important contributions to the development of practical Raman optical activity instruments, were made by Werner Hug of the University of Fribourg, and Lutz Hecht with Laurence Barron at the University of Glasgow.
Theory of Raman optical activity
The basic principle of Raman optical activity is that there is interference between light waves scattered by the polarizability and optical activity tensors of a chiral molecule, which leads to a difference between the intensities of the right- and left-handed circularly polarised scattered beams. The spectrum of intensity differences recorded over a range of wavenumbers reveals information about chiral centres in the sample molecule.
Raman optical activity can be observed in a number of forms, depending on the polarization of the incident and the scattered light. For instance, in the scattered circular polarization (SCP) experiment, the incident light is linearly polarized and differences in circular polarization of the scattered light are measured. In the dual circular polarization (DCP), both the incident and the scattered light are circularly polarized, either in phase (DCPI ) or out of phase (DCPII ).
Biological Raman optical activity spectroscopy
Due to its sensitivity to chirality, Raman optical activity is a useful probe of biomolecular structure and behaviour in aqueous solution. It has been used to study protein, nucleic acid, carbohydrate and virus structures. Though the method does not reveal information to the atomic resolution of crystallographic approaches, it is able to examine structure and behaviour in biologically more realistic conditions (compare the dynamic solution structure examined by Raman optical activity to the static crystal structure).
Related spectroscopic methods
Raman optical activity instruments
A simple introduction to Raman optical activity instruments can be found on Laurence Barron's site . Much of the existing work in the field has utilised custom-made instruments, though commercial instruments are now available.
The thinnest chirality assessed by ROA
The symmetry of the neopentane molecule can be broken if some hydrogen atoms are replaced by deuterium atoms. In particular, if each methyl group has a different number of substituted atoms (0, 1, 2, and 3), one obtains a chiral molecule. The chirality in this case arises solely by the mass distribution of its nuclei, while the electron distribution is still essentially achiral. This chirality is the thinnest one synthesized so far and was assessed by ROA in 2007.
- Nature. 2007 Mar 29. Absolute configuration of chirally deuterated neopentane. Haesler Jacques, Schindelholz Ivan, Riguet Emmanuel, Bochet Christian G, Hug Werner.
- Laurence D. Barron, Fujiang Zhu, Lutz Hecht, George E. Tranter, Neil W. Isaacs, Raman optical activity: An incisive probe of molecular chirality and biomolecular structure, Journal of Molecular Structure, 834–836 (2007) 7–16.
- Laurence D. Barron's ROA page.
- Two Kings of Chirality by Dermot Martin. Laboratory News.http://www.labnews.co.uk/features/two-kings-of-chirality/