Abstract
5-Azidomethyl-2'-deoxyuridine (5-AmdU, 1) has been successfully employed for the metabolic labeling of DNA and fluorescent imaging of live cells. 5-AmdU also demonstrated significant radiosensitization in breast cancer cells via site-specific nitrogen-centered radical (π-aminyl (U-5-CH(2)-NH(•)), 2, and σ-iminyl (U-5-CH═N(•)), 3) formation. This work shows that these nitrogen-centered radicals are not formed via the reduction of the azido group in 6-azidomethyluridine (6-AmU, 4). Radical assignments were performed using electron spin resonance (ESR) in supercooled solutions, pulse radiolysis in aqueous solutions, and theoretical (DFT) calculations. Radiation-produced electron addition to 4 leads to the facile N(3)(-) loss, forming a stable neutral C-centered allylic radical (U-6-CH(2)(•), 5) through dissociative electron attachment (DEA) via the transient negative ion, TNI (U-6-CH(2)-N(3)(•-)), in agreement with DFT calculations. In contrast, TNI (U-5-CH(2)-N(3)(•-)) of 1, via facile N(2) loss (DEA) and protonation from the surrounding water, forms radical 2. Subsequently, 2 undergoes rapid H-atom abstraction from 1 and produces the metastable intermediate α-azidoalkyl radical (U-5-CH(•)-N(3)). U-5-CH(•)-N(3) converts facilely to radical 3. N(3)(-) loss from U-6-CH(2)-N(3)(•-) is thermodynamically controlled, whereas N(2) loss from U-5-CH(2)-N(3)(•-) is dictated by protonation from the surrounding waters and resonance conjugation of the azidomethyl side chain at C5 with the pyrimidine ring.