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Relevance of pi sigma(*) states in the photoinduced processes of adenine, adenine dimer, and adenine-water complexes

Author(s)
Ritze, HHLippert, HSamoylova, ESmith, VRHertel, IVRadloff, WSchultz, Thomas
Issued Date
2005-06
DOI
10.1063/1.1914763
URI
https://scholarworks.unist.ac.kr/handle/201301/57689
Citation
JOURNAL OF CHEMICAL PHYSICS, v.122, no.22
Abstract
Ab initio calculations and time-resolved photoionization spectroscopy were carried out to characterize the role of the lowest two pi sigma(*) excited states for the photoinduced processes in the adenine monomer, adenine dimer, and adenine-water clusters. The calculations show-with respect to the monomer-a stabilization of 0.11-0.14 eV for the pi sigma(*) states in different isomers of adenine dimer and an even bigger stabilization of 0.14-0.36 eV for isomers of adenine-(H2O)(1) and adenine-(H2O)(3). Hence, the stabilized pi sigma(*) states should play an important role in the excited-state relaxation of partially or fully solvated adenine. This conclusion is supported by experimental results: In the adenine monomer, strong n pi(*) state signals are observed. Those signals are reduced in adenine dimer and vanish in water clusters due to the competing relaxation via the pi sigma(*) states.
Publisher
AMER INST PHYSICS
ISSN
0021-9606
Keyword
NUCLEIC-ACID BASESREPULSIVE (1)PI-SIGMA-ASTERISK STATESMOLECULAR-ORBITAL METHODSEXCITED SINGLET-STATESJET-COOLED ADENINEVALENCE BASIS-SETSAB-INITIOHYDROGEN-TRANSFERFLUORESCENCE SPECTROSCOPYNONRADIATIVE DECAY

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