Dynamics of photoinduced processes in adenine and thymine base pairs
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- Dynamics of photoinduced processes in adenine and thymine base pairs
- Samoylova, E.; Lippert, H.; Ullrich, S.; Hertel, I.V.; Radloff, W.; Schultz, Thomas
- RESOLVED PHOTOELECTRON-SPECTROSCOPY; EXCITED-STATE; HYDROGEN-TRANSFER; AB-INITIO; NONRADIATIVE DECAY; LASER SPECTROSCOPY; DNA BASES; IONIZATION; MECHANISM; DIMER
- Issue Date
- AMER CHEMICAL SOC
- JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.127, no.6, pp.1782 - 1786
- The excited-state dynamics of adenine and thymine dimers and the adenine-thymine base pair were investigated by femtosecond pump-probe ionization spectroscopy with excitation wavelengths of 250-272 nm. The base pairs showed a characteristic ultrafast decay of the initially excited ππ* state to an nπ* state (lifetime τππ• ≈ 100 fs) followed by a slower decay of the latter with τnπ* ≈ 0.9 ps for (adenine)2, τnπ* = 6-9 ps for (thymine)2, and τnπ* ≈ 2.4 ps for the adenine-thymine base pair. In the adenine dimer, a competing decay of the ππ* state via the πσ* state greatly suppressed the nπ* state signals. Similarities of the excited-state decay parameters in the isolated bases and the base pairs suggest an intramonomer relaxation mechanism in the base pairs.
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