Competing isomeric product channels in the 193 nm photodissociation of 2-chloropropene and in the unimolecular dissociation of the 2-propenyl radical

被引:39
作者
Mueller, JA
Parsons, BF
Butler, LJ
Qi, F
Sorkhabi, O
Suits, AG
机构
[1] Univ Chicago, James Franck Inst, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
关键词
D O I
10.1063/1.1345877
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
This paper presents product translational energy spectroscopy measurements of the primary photofragmentation channels of 2-chloropropene excited at 193 nm and of the unimolecular dissociation of the 2-propenyl radical. Tunable vacuum ultraviolet (VUV) photoionization of the products allows us to distinguish between the various product isomers formed in these processes. The data show evidence for three significant primary reaction channels in the dissociation of 2-chloropropene: An excited-state C-Cl fission channel producing fast Cl atoms, a C-Cl fission channel producing slow Cl atoms, and HCl elimination. A minor C-CH3 fission channel contributes as well. The measured branching of the major primary product channels is: [fast C-Cl]:[slow C-Cl]:[HCl elimination] = 62%:23%:15%. The experiments also allow us to resolve selectively the product branching between the unimolecular dissociation channels of the 2-propenyl radical, a high energy C3H5 isomer; we measure how the branching ratio between the two competing C-H fission channels changes as a function of the radical's internal energy. The data resolve the competition between the unimolecular H + allene and H+propyne product channels from the radical with internal energies from 0 to 18 kcal/mol above the H + propyne barrier. We find that the barrier to H + allene formation from this high-energy C3H5 radical is higher than the barrier to H+propyne formation, in agreement with recent theoretical calculations but in sharp contrast to that predicted for the most stable C3H5 isomer, the allyl radical. The experiments demonstrate a general technique for selectively forming a particular CnHm isomer dispersed by internal energy due to the primary photolysis, thus allowing us to determine the branching between unimolecular dissociation channels as a function of the selected radical isomer's internal energy. (C) 2001 American Institute of Physics.
引用
收藏
页码:4505 / 4521
页数:17
相关论文
共 47 条
[1]   Emission spectroscopy of jet-cooled CS2 upon excitation of the 1Σg+→1B2(1Σu+) transition in the 48 500-51 000 cm-1 region [J].
Arendt, MF ;
Butler, LJ .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (18) :7835-7843
[2]   TORSIONAL TRANSITIONS AND BARRIERS TO INTERNAL-ROTATION OF THE 2-HALOPROPENES [J].
BELL, S ;
GUIRGIS, GA ;
FANNING, AR ;
DURIG, JR .
JOURNAL OF MOLECULAR STRUCTURE, 1988, 178 :63-78
[3]   CHLOROETHYLENE PHOTOCHEMICAL LASERS - VIBRATIONAL ENERGY CONTENT OF HCL MOLECULAR ELIMINATION PRODUCTS [J].
BERRY, MJ .
JOURNAL OF CHEMICAL PHYSICS, 1974, 61 (08) :3114-3143
[4]   Primary and secondary processes in the 193 nm photodissociation of vinyl chloride [J].
Blank, DA ;
Sun, WZ ;
Suits, AG ;
Lee, YT ;
North, SW ;
Hall, GE .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (13) :5414-5425
[5]   Investigating the C-Cl antibonding character in the pi pi* excited state of vinyl, allyl, and propargyl chloride: Emission spectra and ab initio calculations [J].
Browning, PW ;
Kitchen, DC ;
Arendt, MF ;
Butler, LJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (19) :7765-7771
[6]   PHOTOIONIZATION OF CH3 - HEAT OF FORMATION OF CH2 [J].
CHUPKA, WA ;
LIFSHITZ, C .
JOURNAL OF CHEMICAL PHYSICS, 1968, 48 (03) :1109-&
[7]   Propyne pyrolysis in a flow reactor: An experimental, RRKM, and detailed kinetic modeling study [J].
Davis, SG ;
Law, CK ;
Wang, H .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (30) :5889-5899
[8]   Kinetics and dynamics in the photodissociation of the allyl radical [J].
Deyerl, HJ ;
Gilbert, T ;
Fischer, I ;
Chen, P .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (08) :3329-3332
[9]   Photodissociation dynamics of the allyl radical [J].
Deyerl, HJ ;
Fischer, I ;
Chen, P .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (03) :1450-1462
[10]  
FRANKLIN JL, 1974, ADV MASS SPECTROM, V6, P947