中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Photodissociation dynamics of propionyl chloride in the ultraviolet region

文献类型:期刊论文

作者Wei, Zheng-Rong3; Zhang, Xiao-Peng1,2; Lee, Wei-Bin1,2; Zhang, Bing3; Lin, King-Chuen1,2
刊名JOURNAL OF CHEMICAL PHYSICS
出版日期2009-01-07
卷号130期号:1
关键词ground states molecule-photon collisions photodissociation photoionisation two-photon processes
通讯作者Lin, KC (reprint author), Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan.
英文摘要Velocity imaging technique combined with (2+1) resonance-enhanced multiphoton ionization (REMPI) is used to detect primary photodissociation of propionyl chloride. In one-color experiments at 235 nm, the Cl and Cl-* fragments are produced rapidly, leading to a fraction of translational energy release of 0.37 and 0.35, anisotropy parameters of 1.1 and 0.8, and quantum yield of 0.67 and 0.33, respectively, when initial excitation of the (1)(n, pi(*))(CO) band is coupled to the (1)(n(Cl), sigma(*)(C-Cl)) repulsive configuration. The resulting propionyl radical with sufficient internal energy may undergo secondary dissociation to yield CO that is characteristic of an isotropic distribution. The REMPI spectra of the CO (0,0) and (1,1) bands are measured, giving rise to a Boltzmann rotational temperature of 1200 and 770 K, respectively, and a Boltzmann vibrational temperature of 2800 K. A minor channel of HCl elimination is not detected, probably because of predissociation in two-photon absorption at 235 nm. In two-color experiments comprising an additional 248 nm photolyzing laser, Cl and Cl-* are produced with a fraction of translational energy release of 0.43 and 0.40 and anisotropy parameters of 1.0 and 0.6, respectively. The secondary production of CO is not observed although the internal energy partitioned in the propionyl radical is in the proximity of the dissociation barrier. In either experimental scheme, a small component appearing in the center of the Cl and Cl-* images is proposed to stem from ground state dissociation via internal conversion.
WOS标题词Science & Technology ; Physical Sciences
类目[WOS]Physics, Atomic, Molecular & Chemical
研究领域[WOS]Physics
关键词[WOS]AB-INITIO CALCULATIONS ; C-CL BOND ; ACETYL-CHLORIDE ; NM PHOTODISSOCIATION ; MULTIPHOTON IONIZATION ; MOLECULAR-OXYGEN ; LASER-PULSES ; ALPHA-BOND ; DISSOCIATION ; VELOCITY
收录类别SCI
语种英语
WOS记录号WOS:000262372600012
源URL[http://ir.wipm.ac.cn/handle/112942/2286]  
专题武汉物理与数学研究所_2011年以前论文发表(包括2011年)
作者单位1.Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
2.Acad Sinica, Inst Atom & Mol Sci, Taipei 106, Taiwan
3.Chinese Acad Sci, Wuhan Inst Phys & Math, State Key Lab Magnet Resonance & Atom & Mol Phys, Wuhan 430071, Peoples R China
推荐引用方式
GB/T 7714
Wei, Zheng-Rong,Zhang, Xiao-Peng,Lee, Wei-Bin,et al. Photodissociation dynamics of propionyl chloride in the ultraviolet region[J]. JOURNAL OF CHEMICAL PHYSICS,2009,130(1).
APA Wei, Zheng-Rong,Zhang, Xiao-Peng,Lee, Wei-Bin,Zhang, Bing,&Lin, King-Chuen.(2009).Photodissociation dynamics of propionyl chloride in the ultraviolet region.JOURNAL OF CHEMICAL PHYSICS,130(1).
MLA Wei, Zheng-Rong,et al."Photodissociation dynamics of propionyl chloride in the ultraviolet region".JOURNAL OF CHEMICAL PHYSICS 130.1(2009).

入库方式: OAI收割

来源:武汉物理与数学研究所

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