Dithiooxamide [rubeanic acid, NH2C(S)C(S)NH2)] monomers were studied by FTIR spectroscopy combined with the low-temperature matrix-isolation technique. The most stable dithione−diamino tautomer of the compound was exclusively observed in argon matrixes immediately after deposition. Upon UV (λ > 345 nm) irradiation the dithione−diamino form transformed, by a double-proton transfer, into the dithiol−diimino tauto...
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 spect...
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