Photoinduced dynamics of guanosine monophosphate in water from broad-band transient absorption spectroscopy and quantum-chemical calculations

Abstract

Guanosine monophosphate (GMP) in aqueous solutions has been studied with femtosecond broad-band transient absorption spectroscopy and by quantum-mechanical calculations. The sample was excited at 267 or 287 nm and probed between 270 and 1000 nm with 100 fs resolution, for various pH values between 2 and 7. At pH 2, when the guanine ring is ground-state protonated (GMPH +), we observe isosbestic behavior indicating state-to-state relaxation. The relaxation is biexponential, τ 1 = 0.4 ps, τ 2 = 2.2 ps, and followed by slower internal conversion with τ 3 = 167 ps. For nonprotonated GMP in the pH range 7-4, we find biexponential decay in the region 400-900 nm (τ 1 = 0.22 ps, τ 2 = 0.9 ps), whereas, between 270 and 400 nm, the behavior is triexponential with one growing, τ 1 = 0.25 ps, and two decaying, τ 2 = 1.0 ps, τ 3 = 2.5 ps, components. The excited-state evolution is interpreted with the help of quantumchemical calculations, performed at the time-dependent PBE0 level accounting for bulk solvent effects and specific solvation. The computed dynamics involves L a and L b bright excited states, whereas the n 0 π and π σ dark excited states play a minor role. Independent of the pH, the photoinduced evolution involves ultrafast L b → L a conversion (τ ba « 100 fs) and exhibits the presence of a wide planar plateau on L a. For neutral GMP a barrierless path connects this region to a conical intersection (CI) with the ground state, giving an account of the ultrafast decay of this species. For protonated GMPH + the system evolves into a stable minimum L a min characterized by out-of-plane displacement of NH and CH groups, which explains the longer (167 ps) fluorescence lifetime. © 2009 American Chemical Society.