## Abstract The circular dichroism of double‐helical nucleic acids was calculated as a function of geometry, including terms involving __n__ → π\* transitions. The “nonbonding” __n__ or σ orbitals were of the azine type, delocalized, but concentrated at the nitrogen atoms of the purines and pyrimid
Calculations of the circular dichroism of double-helical nucleic acids. I. Effects involving π → π* transitions
✍ Scribed by David S. Studdert; Robert C. Davis
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1974
- Tongue
- English
- Weight
- 657 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
The circular dichroism of double‐helical nucleic acids was calculated as a function of geometry using the theory of Tinoco and Johnson. This theory does not include contributions of near ultraviolet transitions that are not π → π* in nature. The calculated circular dichroism shows a strong dependence on the distance of base pairs from the helix axis and the tilt of the base pair. Smaller dependences are predicted for the propeller‐like twist of a base pair and for variation of the angular increment per base pair. Moderately good agreement between calculated and many experimentally observed spectra could be generated.
📜 SIMILAR VOLUMES
## Abstract The circular dichroism of double‐helical nucleic acids was calculated using three different sets of wave functions for the purine and pyrimidine chromophores. Different wave functions give qualitatively the same types of spectra. Quantitatively, the differences are very substantial. How
On page 1533, in the last term of eq. (2), (alm[O) should be (alml0). On page 1538, in line 3 of the Results section, R,,\* should be Rn,\*; in the next line, RB should also be Rn,\*, and the first "in" should be "is.