Analysis of ultrafast relaxation in photoexcited DNA base pairs of adenine and thymine

被引:32
|
作者
Samoylova, E. [1 ]
Schultz, T. [1 ]
Hertel, I. V. [1 ]
Radloff, W. [1 ]
机构
[1] Max Born Inst Nichtlineare Opt & Kurzzeitspekt, D-12489 Berlin Adlershof, Germany
关键词
adenine; thymine; excited state relaxation; internal conversion; time-resolved spectroscopy; multiphoton ionization; DNA photochemistry;
D O I
10.1016/j.chemphys.2007.09.046
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photoinduced dynamics in base pairs of adenine and thymine were analyzed by femtosecond pump-probe spectroscopy. On the short-time scale up to a few picoseconds, the characteristic time constants for the dimers are quite similar to the corresponding values of the monomers. This leads to the conclusion that ultrafast intramolecular relaxation proceeds via pi pi* and n pi* states of one component within the dimer. On the long-time scale, we obtained a novel time constant of roughly 40 ps for the thymine dimer and the adenine-thymine base pair. This time constant was never observed in the monomers and is tentatively assigned to an intermolecular relaxation process, possibly via a hydrogen transfer state. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:376 / 382
页数:7
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