Shape resonance spectra of uracil, 5-fluorouracil, and 5-chlorouracil

被引:51
|
作者
Kossoski, F. [1 ]
Bettega, M. H. F. [2 ]
Varella, M. T. do N. [1 ]
机构
[1] Univ Sao Paulo, Inst Fis, BR-05314970 Sao Paulo, Brazil
[2] Univ Fed Parana, Dept Fis, BR-81531990 Curitiba, Parana, Brazil
来源
JOURNAL OF CHEMICAL PHYSICS | 2014年 / 140卷 / 02期
基金
巴西圣保罗研究基金会;
关键词
DISSOCIATIVE ELECTRON-ATTACHMENT; LOW-ENERGY ELECTRONS; NEGATIVE-IONS; RADIATION-DAMAGE; DNA; SCATTERING; BASES; 5-HALOURACILS; MOLECULES; PSEUDOPOTENTIALS;
D O I
10.1063/1.4861589
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
We report on the shape resonance spectra of uracil, 5-fluorouracil, and 5-chlorouracil, as obtained from fixed-nuclei elastic scattering calculations performed with the Schwinger multichannel method with pseudopotentials. Our results are in good agreement with the available electron transmission spectroscopy data, and support the existence of three pi* resonances in uracil and 5-fluorouracil. As expected, the anion states are more stable in the substituted molecules than in uracil. Since the stabilization is stronger in 5-chlorouracil, the lowest pi* resonance in this system becomes a bound anion state. The present results also support the existence of a low-lying sigma(CCl)* shape resonance in 5-chlorouracil. Exploratory calculations performed at selected C-Cl bond lengths suggest that the sigma(CCl)* resonance could couple to the two lowest pi* states, giving rise to a very rich dissociation dynamics. These facts would be compatible with the complex branching of the dissociative electron attachment cross sections, even though we cannot discuss any details of the vibration dynamics based only on the present fixed-nuclei results. (c) 2014 AIP Publishing LLC.
引用
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页数:7
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