OSU Navigation Bar

The Ohio State University University Libraries Knowledge Bank

VIBRONIC INTERACTIONS - DOMINANT FACTOR IN THE VIBRATIONAL SPECTRA OF CONJUGATED RADICAL ANION SALTS

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/16065

Show full item record

Files Size Format View
1973-M-11.jpg 190.9Kb JPEG image Thumbnail of VIBRONIC INTERACTIONS - DOMINANT FACTOR IN THE VIBRATIONAL SPECTRA OF CONJUGATED RADICAL ANION SALTS

Title: VIBRONIC INTERACTIONS - DOMINANT FACTOR IN THE VIBRATIONAL SPECTRA OF CONJUGATED RADICAL ANION SALTS
Creators: Hinkel, Jerry; Devlin, J. Paul
Issue Date: 1973
Abstract: Raman spectra for the intensely colored salts of the tetracyanoethylene radical anion with sodium and potassium cations confirm previous assertions that the infrared salt spectra are completely dominated by vibronic interaction effects. As expected, strong Raman scattering has been observed at frequencies coincident with the intense infrared bands which have been assigned to totally symmetric modes activated by an ``electron-vibration” moment. Such coincidences are also common for the anion and dianion of anthracene. Further, the scattering intensities of the symmetric stretching modes reveal a complex dependence on excitation frequency which is qualitatively consistent with the observed vibronic structure of the electronic absorption bands. By confirming the assignment of several of the radical anion internal modes, the Raman data have also permitted the evaluation of reliable stretching constants for comparison with the neutral molecule force constants and quantum chemical predictions of bond order changes.
URI: http://hdl.handle.net/1811/16065
Other Identifiers: 1973-M-11
Bookmark and Share