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在强飞秒近红外激光场中产生的乙烷二价阳离子的亚稳态分解和氢迁移。

Metastable decomposition and hydrogen migration of ethane dication produced in an intense femtosecond near-infrared laser field.

机构信息

Faculty of Pharmaceutical Science, Niigata University of Pharmacy and Applied Life Sciences, 265-1 Higashijima, Akiha-ku, Niigata-city 956-8603, Japan.

出版信息

J Chem Phys. 2011 Feb 14;134(6):064324. doi: 10.1063/1.3549137.

DOI:10.1063/1.3549137
PMID:21322697
Abstract

We investigated a formation channel of triatomic molecular hydrogen ions from ethane dication induced by irradiation of intense laser fields (800 nm, 100 fs, ∼1 × 10(14) W∕cm(2)) by using time of flight mass spectrometry. Hydrogen ion and molecular hydrogen ion (H,D)(n)(+) (n = 1-3) ejected from ethane dications, produced by double ionization of three types of samples, CH(3)CH(3), CD(3)CD(3), and CH(3)CD(3), were measured. All fragments were found to comprise components with a kinetic energy of ∼3.5 eV originating from a two-body Coulomb explosion of ethane dications. Based on the signal intensities and the anisotropy of the ejection direction with respect to the laser polarization direction, the branching ratios, H(+):D(+) = 66:34, H(2)(+):HD(+):D(2)(+) = 63:6:31, and H(3)(+):H(2)D(+):HD(2)(+):D(3)(+) = 26:31:34:9 for the decomposition of C(2)H(3)D(3)(2+), were determined. The ratio of hydrogen molecules, H(2):HD:D(2) = 31:48:21, was also estimated from the signal intensities of the counter ion C(2)(H,D)(4)(2+). The similarity in the extent of H∕D mixture in (H,D)(3)(+) with that of (H,D)(2) suggests that these two dissociation channels have a common precursor with the C(2)H(4)(2+)...H(2) complex structure, as proposed theoretically in the case of H(3)(+) ejection from allene dication [A. M. Mebel and A. D. Bandrauk, J. Chem. Phys. 129, 224311 (2008)]. In contrast, the (H,D)(2)(+) ejection path with a lower extent of H∕D mixture and a large anisotropy is expected to proceed essentially via a different path with a much rapid decomposition rate. For the Coulomb explosion path of C-C bond breaking, the yield ratios of two channels, CH(3)CD(3)(2+)→ CH(3)(+) + CD(3)(+) and CH(2)D(+) + CHD(2)(+), were 81:19 and 92:8 for the perpendicular and parallel directions, respectively. This indicates that the process occurs at a rapid rate, which is comparable to hydrogen migration through the C-C bond, resulting in smaller anisotropy for the latter channel that needs H∕D exchange.

摘要

我们通过飞行时间质谱法研究了强激光场(800nm,100fs,约 1×10(14)W∕cm(2))照射下乙烷二价离子诱导的三原子分子氢离子的形成通道。测量了从三种类型的样品(CH(3)CH(3)、CD(3)CD(3)和 CH(3)CD(3))的双电离产生的乙烷二价离子中喷射出的氢离子和分子氢离子(H,D)(n)(+)(n=1-3)。所有碎片都被发现包含源自乙烷二价离子的两个体库仑爆炸的动能约为 3.5eV 的组分。基于信号强度和相对于激光偏振方向的喷射方向的各向异性,确定了 C(2)H(3)D(3)(2+)分解的分支比 H(+):D(+) = 66:34、H(2)(+):HD(+):D(2)(+) = 63:6:31 和 H(3)(+):H(2)D(+):HD(2)(+):D(3)(+) = 26:31:34:9。从抗衡离子 C(2)(H,D)(4)(2+)的信号强度还估计了氢气分子 H(2):HD:D(2) = 31:48:21 的比值。(H,D)(3)(+)中 H∕D 混合物的程度与(H,D)(2)相似,这表明这两个解离通道具有共同的前体,其结构与理论上烯丙二价离子中 H(3)(+)喷射提出的 C(2)H(4)(2+)...H(2)复合物结构相似[A.M.Mebel 和 A.D.Bandrauk,J.Chem.Phys.129,224311(2008)]。相比之下,预计具有较低 H∕D 混合物程度和较大各向异性的(H,D)(2)(+)喷射路径将通过具有更快分解速率的不同路径基本进行。对于 C-C 键断裂的库仑爆炸路径,两个通道的产率比 CH(3)CD(3)(2+)→CH(3)(+) + CD(3)(+)和 CH(2)D(+) + CHD(2)(+)分别为垂直和平行方向的 81:19 和 92:8。这表明该过程发生的速度很快,与氢通过 C-C 键迁移的速度相当,导致后者通道的各向异性较小,因为后者通道需要 H∕D 交换。

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