Document details

Photochemical Ring-Opening Reaction in 2(1H)-Pyrimidinones: A Matrix Isolation...

Author(s): Lapinski, Leszek cv logo 1 ; Rostkowska, Hanna cv logo 2 ; Khvorostov, Artem cv logo 3 ; Fausto, Rui cv logo 4 ; Nowak, Maciej J. cv logo 5

Date: 2003

Persistent ID: http://hdl.handle.net/10316/10678

Origin: Estudo Geral - Universidade de Coimbra


Description
Photoreactions induced by UV-B (290−320 nm) irradiation were studied for 1-methyl-2(1H)-pyrimidinone and 1-methylcytosine monomers isolated in low-temperature inert gas matrixes. A Norrish type I α-cleavage reaction leading to open-ring conjugated isocyanate was observed for 1-methyl-2(1H)-pyrimidinone. The structure of the photoproduct was identified by comparison of its experimental IR spectrum with the spectrum theoretically calculated at the DFT(B3LYP)/6-31++G(d,p) level. The main indication of isocyanate as a photoproduced species was the appearance in the infrared spectrum recorded after UV irradiation of a very strong band at a characteristic frequency of 2263 cm-1. Observation of a new band at nearly the same frequency in the spectrum of UV-irradiated monomeric 1-methylcytosine may suggest that also in the case of this compound a conjugated isocyanate is photoproduced. http://dx.doi.org/10.1021/jp035155i
Document Type Article
Language English
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