R;?mnn spectra of liquid mixtures of TCNE with aromatic tlecWm donors were studied. Red-shifts up lo 20 cm-' and changes in the intensity ratio of the C=C and C=N stretching modes of TCNE from 0.5 to 1.5-3.0 upon complexation were observed and related to an electron transfer of up to 9 % in the Boun
Interpretation of hypochromic and hyperchromic intensity changes in the Raman spectra of polypeptides and polynucleotides undergoing transition
β Scribed by P. C. Painter; J. L. Koenig
- Book ID
- 102764702
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1976
- Tongue
- English
- Weight
- 806 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Abstract
The hyperchromic and hypochromic changes in the intensity of the amideβI and amideβIII lines of polypeptides and certain ring vibrations of the bases of polynucleotides are shown to be related to similar changes in the lower energy uv absorption bands. The selection rules strictly limit the pairs of excited electronic states that can contribute to the elements of the polarizability matrix. An energyβdependent term in this equation weights the contribution of the pairs of electronic transitions in favor of those involving the lower energy transitions. For both polypeptides and polynucleotides, there is a large hypochromic inensity change in the first Ο β Ο* exciton band upon the coilβtoβhelix transition. Through the selection rules, certain conformationally sensitive Raman lines are shown to derive their intensity predominantly from this band and hence also display hypochromism. Again, through an application of the selection rules, certain Raman lines can be demonstrated to depend predominantly for their intensity upon the n β Ο* transition, and consequently have the opposite hyperchromic intensity change upon the same conformational transition.
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