Rumyana I Bakalska, Vassil B Delchev
Index: J. Mol. Model. 18(12) , 5133-46, (2012)
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An experimental and theoretical investigation was performed to study the photostability of cytosine and isocytosine. The experimental UV irradiation of acetonitrile solutions of the two compounds showed that the amino-oxo tautomer of cytosine is photostable while the amino-oxo tautomer of isocytosine tautomerizes to the amino-hydroxy form. The theoretical investigations were carried out at the CC2 level of theory. They were performed to explain the experimental observations. It was found that the (1)ππ(*) excited states of the ring deformation mechanisms of cytosine and isocytosine relax (internal conversion) to the ground states of the amino-oxo forms of the compounds. We propose a channel for the radiationless deactivation of the repulsive (1)πσ(*) excited state of the amino-oxo form of isocytosine to the ground state of the amino-hydroxy tautomer.
Structure | Name/CAS No. | Molecular Formula | Articles |
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Isocytosine
CAS:108-53-2 |
C4H5N3O |
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1996-12-01 [J. Mol. Evol. 43(6) , 543-50, (1996)] |
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