Infrared Photodissociation Spectroscopic and Theoretical Study of the HC2n O+ (n=3-6) Cations

被引:4
|
作者
Li, Wei [1 ]
Jin, Jia-ye [1 ]
Qu, Hui [1 ]
Wang, Guan-jun [1 ]
Zhou, Ming-fei [1 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon chain cations; Linear carbon chain derivatives; Infrared spectroscopy; Density functional theory; Interstellar species; CARBON CHAINS; MICROWAVE SPECTROSCOPY; HYPERFINE-STRUCTURE; ROTATIONAL SPECTRA; LASER SPECTROSCOPY; MOLECULES; RADICALS; BORON; RINGS; HCCCO;
D O I
10.1063/1674-0068/cjcp1811254
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The carbon chain cations, HC2n O+ (n=3-6) are produced via a pulsed laser vaporization supersonic expansion ion source in the gas phase. Their infrared spectra are measured via mass-selected infrared photodissociation spectroscopy of the CO "tagged" [HC2n O center dot CO](+) cation complexes in 1600-3500 cm(-1) frequency range. The geometric and electronic structures of the [HC2nO center dot CO](+) complexes and the core HC2n O+ (n=3-6) cations are determined with the aid of density functional theory calculations. These HC2n O+ (n=3-6) ions are identified to be linear carbon chain derivatives terminally capped by hydrogen and oxygen. The triplet ground states are 10-15 kcal/mol lower in energy than the singlet states, indicating cumulene-like carbon chain structures.
引用
收藏
页码:77 / 83
页数:7
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