The effect of C5 substitution on the photochemistry of uracil

0351531 - ÚOCHB 2011 RIV GB eng J - Článek v odborném periodiku
Nachtigallová, Dana - Lischka, Hans - Szymczak, J. J. - Barbatti, M. - Hobza, Pavel - Gengeliczki, Z. - Pino, G. - Callahan, M. P. - Vries de, M. S.
The effect of C5 substitution on the photochemistry of uracil.
Physical Chemistry Chemical Physics. Roč. 12, č. 19 (2010), s. 4924-4933. ISSN 1463-9076. E-ISSN 1463-9084
Grant CEP: GA MŠMT LC512
Výzkumný záměr: CEZ:AV0Z40550506
Klíčová slova: excited-state lifetime * IR/UV double-resonant spectroscopy * multi-reference ab initio methods * uracil analogues
Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
Impakt faktor: 3.454, rok: 2010

A combined experimental and theoretical study on the excited-state behavior of the uracil analogues, 5-OH-Ura and 5-NH2-Ura is reported. Two-photon ionization and IR/UV double-resonant spectra show that there is only one tautomer present for each with an excited state lifetime of 1.8 ns for 5-OH-Ura and 12.0 ns for 5-NH2-Ura as determined from pump–probe experiments. The nature of the excited states of both species is investigated by means of multi-reference ab initio methods. Vertical excitation energies, excited state minima, minima on the crossing seam and reaction paths towards them are determined. Sizeable barriers on these paths are found that provide an explanation for the lifetimes of several nanoseconds observed in the experiment.
Trvalý link: http://hdl.handle.net/11104/0191265