SIGNIFICANCE OF THE PHENYL GROUP FOR THE DIPOLE STRENGTHS AND ROTATIONAL STRENGTHS IN DEUTERATED PHENYLETHANES

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/11641

Show full item record

Files Size Format View
1981-RG-03.jpg 89.17Kb JPEG image Thumbnail of SIGNIFICANCE OF THE PHENYL GROUP FOR THE DIPOLE STRENGTHS AND ROTATIONAL STRENGTHS IN DEUTERATED PHENYLETHANES

Title: SIGNIFICANCE OF THE PHENYL GROUP FOR THE DIPOLE STRENGTHS AND ROTATIONAL STRENGTHS IN DEUTERATED PHENYLETHANES
Creators: Havel, Henry A.; Abbate, S.; Laux, Leo J.; Pultz, Vaughan M.; Overend, John; Moscowitz, Albert
Issue Date: 1981
Publisher: Ohio State University
Abstract: Measurements of the circular dichroism spectra in the 3-5 $\mu$m region have now been completed for the entire series of molecules $S-(+)-Ph-CHC-X (X = CH_{3}, CH_{2}D, CD_{2}H, CD_{3}).^{1}$ Charge-flow $model^{2}$ calculations of the dipole strengths in the aliphatic CH and CD stretching modes do not depend strongly on the details of the phenyl moiety. In contrast charge-flow model calculations of the corresponding rotational strengths show the importance of including the phenyl group explicitly when interpreting the observed VCD spectra. More specifically, our calculations indicate that electronic charge rearrangement in the phenyl group resulting from aliphatic CH and CD motions contributes significantly to the observed rotational strengths.
Description: $^{1}$ R. L. Elsenbaumer and H. S. Mosher, J. Org. Chem. 44, 600 (1979). $^{2}$S. Abbate, L. Laux, J. Overend and A. Moscowitz, 35th Symposium on Molecular Spectroscopy, Columbus, Ohio, 1980, paper RG1.
Author Institution:
URI: http://hdl.handle.net/1811/11641
Other Identifiers: 1981-RG-3
Bookmark and Share