Electronic Absorption Spectra of Protonated Pyrene and Coronene in Neon Matrixes

被引:39
|
作者
Garkusha, Iryna [1 ]
Fulara, Jan [1 ,2 ]
Sarre, Peter J. [3 ]
Maier, John P. [1 ]
机构
[1] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
[2] Polish Acad Sci, Inst Phys, PL-02668 Warsaw, Poland
[3] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2011年 / 115卷 / 40期
基金
瑞士国家科学基金会;
关键词
DIFFUSE INTERSTELLAR BANDS; GAUSSIAN-BASIS SETS; POLYCYCLIC AROMATIC-HYDROCARBONS; INFRARED-SPECTRA; RADICAL CATIONS; CARBONIUM-IONS; GAS-PHASE; ATOMS LI; BENZENE; RESOLUTION;
D O I
10.1021/jp206188a
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
Protonated pyrene and coronene have been isolated in 6 K neon matrixes. The cations were produced in the reaction of the parent aromatics with protonated ethanol in a hot-cathode discharge source, mass selected, and co-deposited with neon. Three electronic transitions of the most stable isomer of protonated pyrene and four of protonated coronene were recorded. The strongest, S-1 -> S-0 transitions, are in the visible region, with onset at 487.5 nm for protonated pyrene and 695.6 nm for protonated coronene. The corresponding neutrals were also observed. The absorptions were assigned on the basis of ab initio coupled-cluster and time-dependent density functional theory calculations. The astrophysical relevance of protonated polycyclic aromatic hydrocarbons is discussed.
引用
收藏
页码:10972 / 10978
页数:7
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