The kinetic method was applied to the determination of the proton affinities (PAs) of modified deoxy-and dideoxyribonucleosides. A correlation between the measured PAs and the replacement of one of the three hydroxyl groups of the ribose unit is presented. A PA scale was obtained which shows that th
Infrared Spectra of Protonated Uracil, Thymine and Cytosine
✍ Scribed by Jean-Yves Salpin; Sébastien Guillaumont; Jeanine Tortajada; Luke MacAleese; Joël Lemaire; Philippe Maitre
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 488 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1439-4235
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✦ Synopsis
Abstract
The gas‐phase structures of protonated uracil, thymine, and cytosine are probed by using mid‐infrared multiple‐photon dissociation (IRMPD) spectroscopy performed at the Free Electron Laser facility of the Centre Laser Infrarouge d′Orsay (CLIO), France. Experimental infrared (IR) spectra are recorded for ions that were generated by electrospray ionization, isolated, and then irradiated in a quadrupole ion trap; the results are compared to the calculated infrared absorption spectra of the different low‐lying isomers (computed at the B3LYP/6‐31++G(d,p) level). For each protonated base, the global energy minimum corresponds to an enolic tautomer, whose infrared absorption spectrum matched very well with the experimental IRMPD spectrum, with the exception of a very weak IRMPD signal observed at about 1800 cm^−1^ in the case of the three protonated bases. This signal is likely to be the signature of the second‐energy‐lying oxo tautomer. We thus conclude that within our experimental conditions, two tautomeric ions are formed which coexist in the quadrupole ion trap.
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