Observation of a transition state resonance in the integral cross section of the F+HD reaction

被引:199
作者
Skodje, RT [1 ]
Skouteris, D
Manolopoulos, DE
Lee, SH
Dong, F
Liu, K
机构
[1] Acad Sinica, Inst Atom & Mol Sci, Taipei 106, Taiwan
[2] Univ Colorado, Dept Chem, Boulder, CO 80309 USA
[3] Phys & Theoret Chem Lab, Oxford OX1 3QZ, England
关键词
D O I
10.1063/1.481041
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
We have studied the reaction F + HD at low collision energies using a combination of experimental and theoretical methods. Clear evidence for a reactive resonance is found in the integral cross section for the reactive channel F + HD --> HF + D. Using a crossed molecular beam apparatus, the total reactive cross sections for the HF + D and DF + H channels were obtained in the collision energy range of 0.2-5 kcal/mol. In addition, Doppler profiles were obtained over this range of energies, which provide information about the angularly resolved distribution of final vibrational states. The cross section shows a distinctive steplike feature near 0.5 kcal/mol. Furthermore, the Doppler profiles reveal a dramatic change in the angular distribution of products over a narrow energy range centered at 0.5 kcal/mol. This feature is shown to arise from a reactive resonance localized near the transition state. Theoretical scattering calculations have been carried out using the Stark-Werner potential energy surface, which accurately reproduce the shape of the resonance feature. A detailed analysis of quantum dynamics using the spectral quantization method reveals that a quantum resonance exists near 0.52 kcal/mol, which is localized about the collinear FHD geometry. At collision energies below 1 kcal/mol, the reaction was found to proceed almost exclusively through resonant tunneling with very little contribution from direct, over the barrier, reaction. The properties of the quantum resonance, such as the position, lifetime, and partial widths were found to correlate well with the experimental results and the quantum scattering calculations. (C) 2000 American Institute of Physics. [S0021-9606(00)00709-1].
引用
收藏
页码:4536 / 4552
页数:17
相关论文
共 81 条
[71]   An accurate multireference configuration interaction calculation of the potential energy surface for the F+H-2->HF+H reaction [J].
Stark, K ;
Werner, HJ .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (17) :6515-6530
[72]   van der Waals resonances in cumulative reaction probabilities for the F+H2, D2, and HD reactions [J].
Takayanagi, T ;
Kurosaki, Y .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (20) :8929-8934
[73]   STABILIZATION CALCULATIONS AND PROBABILITY DENSITIES FOR THE WELL-STUDIED COLLISIONAL RESONANCES IN COLLINEAR F+H2, F+HD, AND F+D2 [J].
THOMPSON, TC ;
TRUHLAR, DG .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (02) :210-214
[74]   EXACT AND APPROXIMATE QUANTUM MECHANICAL REACTION PROBABILITIES AND RATE CONSTANTS FOR COLLINEAR H + H2 REACTION [J].
TRUHLAR, DG ;
KUPPERMANN, A .
JOURNAL OF CHEMICAL PHYSICS, 1972, 56 (05) :2232-+
[75]  
TRUHLAR DG, 1984, ACS S SERIES, V263
[76]   Spectral quantization of transition state resonances in collinear Mu+H-2 and Mn+D-2 collisions [J].
Varandas, AJC ;
Yu, HG .
CHEMICAL PHYSICS, 1996, 209 (01) :31-40
[77]   THRESHOLD PHOTODETACHMENT SPECTROSCOPY OF THE I+HI TRANSITION-STATE REGION [J].
WALLER, IM ;
KITSOPOULOS, TN ;
NEUMARK, DM .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (06) :2240-2242
[78]  
WEAVER A, 1991, FARADAY DISCUSS, V91, P5
[79]   QUANTUM-MECHANICAL COMPUTATIONAL STUDIES OF CHEMICAL REACTIONS .3. COLLINEAR A+BC REACTION WITH SOME MODEL POTENTIAL-ENERGY SURFACES [J].
WU, SF ;
JOHNSON, BR ;
LEVINE, RD .
MOLECULAR PHYSICS, 1973, 25 (04) :839-856
[80]  
WYATT RE, 1982, BER BUNSEN PHYS CHEM, V86, P437, DOI 10.1002/bbpc.19820860519