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Excimer states in microhydrated adenine clusters

Author(s)
Smith, V. R.Samoylova, E.Ritze, H. -H.Radloff, W.Schultz, Thomas
Issued Date
2010-09
DOI
10.1039/c003967e
URI
https://scholarworks.unist.ac.kr/handle/201301/6237
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77955879939
Citation
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, v.12, no.33, pp.9632 - 9636
Abstract
We present femtosecond pump-probe mass and photoelectron spectra for adenine (A) and microhydrated A(m)(H(2)O)(n) clusters. Three distinct relaxation processes of photoexcited electronic states were distinguished: in unhydrated A, relaxation of the optically bright pi pi* state occurred via the dark n pi* state with respective lifetimes of <0.1 and 1.3 ps. In microhydrated clusters A(H(2)O)(n), relaxation via the n pi* state is quenched by a faster relaxation process, probably involving pi sigma* states. For the predominantly hydrogen-bonded adenine dimer (A(2)), excited state relaxation is dominated by monomer-like processes. When the adenine dimer is clustered with several water molecules, we observe a nanosecond lifetime from excimer states in pi-stacked clusters. From the electron spectra we estimate adiabatic ionization potentials of 8.32 eV (A), 8.27 eV (A(H(2)O)(1)), 8.19 eV (A(H(2)O)(2)), 8.10 eV (A(H(2)O)(3)), 8.18 eV (A(2)), and 8.0 eV (A(2)(H(2)O)(3-5)).
Publisher
ROYAL SOC CHEMISTRY
ISSN
1463-9076

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