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VIBRATIONAL CIRCULAR DICHOROSISM AS A CRITERION FOR LOCAL MODE VERSUS NORMAL MODE BEHAVIOR

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/16989

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Title: VIBRATIONAL CIRCULAR DICHOROSISM AS A CRITERION FOR LOCAL MODE VERSUS NORMAL MODE BEHAVIOR
Creators: Abbate, S.; Longhi, G.; Richard, L.; Bertucci, C.; Rosini, C.; Salvadori, P.; Moscowitz, Albert
Issue Date: 1986
Abstract: The local mode approach frequently permits a straight forward and appealing interpretation of near infrared and visible vibrational spectra of the higher ovetoones of organic $molecules.^{(1)}$ Vibrational circular dichroism (VCD) spectra have the potential to distinguish radily between local mode and normal mode behavior. This is so because the kinetic and potential energy coulings that lead to normal mode behavior are frequentuly crucial for the generation of significant VCD intensity. To test this concept, we have undertaken a VCD study in the spectral region 1000-800 mm of terpenes and related molecules. The molecules are of the sort whose VCD spectra have been studied extensively in the CH-stretching fundamental region by Laux $et al. ^{(2)}$ The concept seems ti be a sueful one. For example, we find that (R)-(+)-limonene and its enantiomer exhibit circular dichroism for the thrid overtone that can be attributed to normal modes of the sort discussed in reference 2: on the other hand, we can detect no VCD intensity in the analogous transition of (-)-menthone.
URI: http://hdl.handle.net/1811/16989
Other Identifiers: 1986-RC-9
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