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dc.creatorHarris, W. C.en_US
dc.creatorLevin, Ira W.en_US
dc.date.accessioned2006-06-15T13:33:14Z
dc.date.available2006-06-15T13:33:14Z
dc.date.issued1972en_US
dc.identifier1972-Q-10en_US
dc.identifier.urihttp://hdl.handle.net/1811/9094
dc.descriptionPresent address of William C. Harris: Department of Chemistry, Furman University, Greenville, South Carolina 29613. $^{1}$ See, for example, N.L. Allinger, M.T. Tribble, M. Miller and D.H. Wertz, J. Amer. Chem. Soc. 93, 1636 (1971).""en_US
dc.descriptionAuthor Institution: National Institute of Arthrities and Metabolic Diseases, National Institute of Healthen_US
dc.description.abstractIn recent years, various investigators have demonstrated the practicality of calculating minimum energy conformations and strain energies for hydrocarbons and related $molecules.^{1}$ The success, however, of accurately determining structures by this method requires a moderately detailed knowledge of representative potential functions. For this reason, the method is limited to systems that are not highly strained. Since virtually no vibrational information exists for bicyclic molecules, we have undertaken investigations on a series of these hydrocarbons with the goal both of understanding their spectra and of determining a suitable potential function for use in the conformational calculation of strained systems. In the present study we discuss the infrared and Raman spectra of norbornane and nor-bornadiene (strain energies of 18.4 and 29.0 kcal/mole, respectively) and present a valence force field for assessing the consistency of the vibrational assignment.en_US
dc.format.extent163411 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titleINTERPRETATION OF THE VIBRATIONAL SPECTRA OF STRAINED BICYCLIC RING SYSTEMS: NORBORNANE AND NORBORNADIENEen_US
dc.typearticleen_US


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