Internal conversion and intersystem crossing pathways in UV excited, isolated uracils and their implications in prebiotic chemistry

被引:71
作者
Yu, Hui [1 ]
Sanchez-Rodriguez, Jose A. [1 ]
Pollum, Marvin [2 ,3 ]
Crespo-Hernandez, Carlos E. [2 ,3 ]
Mai, Sebastian [4 ]
Marquetand, Philipp [4 ]
Gonzalez, Leticia [4 ]
Ullrich, Susanne [1 ]
机构
[1] Univ Georgia, Dept Phys & Astron, Athens, GA 30602 USA
[2] Case Western Reserve Univ, Dept Chem, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Ctr Chem Dynam, Cleveland, OH 44106 USA
[4] Univ Vienna, Inst Theoret Chem, Fac Chem, Wahringer Str 17, A-1090 Vienna, Austria
基金
奥地利科学基金会; 美国国家科学基金会;
关键词
TIME-RESOLVED PHOTOELECTRON; THYMINE BASE-PAIRS; RELAXATION DYNAMICS; STATE DYNAMICS; AB-INITIO; GAS-PHASE; PHOTOINDUCED PROCESSES; ELECTRONIC RELAXATION; ULTRAFAST RELAXATION; PHOTOEXCITED DNA;
D O I
10.1039/c6cp01790h
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 photodynamic properties of molecules determine their ability to survive in harsh radiation environments. As such, the photostability of heterocyclic aromatic compounds to electromagnetic radiation is expected to have been one of the selection pressures influencing the prebiotic chemistry on early Earth. In the present study, the gas-phase photodynamics of uracil, 5-methyluracil (thymine) and 2-thiouracil-three heterocyclic compounds thought to be present during this era-are assessed in the context of their recently proposed intersystem crossing pathways that compete with internal conversion to the ground state. Specifically, time-resolved photoelectron spectroscopy measurements evidence femtosecond to picosecond timescales for relaxation of the singlet (1)pi pi* and (1)n pi* states as well as for intersystem crossing to the triplet manifold. Trapping in the excited triplet state and intersystem crossing back to the ground state are investigated as potential factors contributing to the susceptibility of these molecules to ultraviolet photodamage.
引用
收藏
页码:20168 / 20176
页数:9
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