Mode-correlated product pairs in the F+CHD3→DF+CHD2 reaction

被引:71
作者
Zhou, JG
Lin, JJ
Liu, KP
机构
[1] Acad Sinica, Inst Atom & Mol Sci, Taipei 106, Taiwan
[2] Natl Tsing Hua Univ, Dept Appl Chem, Hsinchu 300, Taiwan
[3] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
关键词
D O I
10.1063/1.1611877
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
The title reaction was investigated at three different collision energies in a pulsed, crossed-beam apparatus. The (2+1) REMPI spectra of the CHD2 products revealed, in addition to the anticipated 4(m)(n) vibronic bands, a hitherto unobserved feature. The new feature was shown and assigned to the 3(1)(1) band. A time-sliced ion velocity imaging technique was applied to map out the coincident DF attributes of the two product states 4(2) and 3(1), whose energy levels lie nearly degenerate. Remarkably similar results were found for the two states in every aspect at all three collision energies. A simple model of Fermi-coupled states was proposed to rationalize this, at first sight, surprising finding. Implications to collisional processes which involve mixed molecular basis states in general are outlined. Possible quantum interference phenomenon is suggested. (C) 2003 American Institute of Physics.
引用
收藏
页码:8289 / 8296
页数:8
相关论文
共 24 条
[1]   Controlling bond cleavage and probing intramolecular dynamics via photodissociation of rovibrationally excited molecules [J].
Bar, I ;
Rosenwaks, S .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 2001, 20 (04) :711-749
[2]   ELECTRONIC-SPECTRA OF THE HETEROISOTOPIC CH2D AND CHD2 RADICALS BY RESONANCE ENHANCED MULTIPHOTON IONIZATION [J].
BRUM, JL ;
JOHNSON, RD ;
HUDGENS, JW .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (05) :3732-3736
[3]   ROVIBRONIC 2-PHOTON TRANSITIONS OF SYMMETRIC TOP MOLECULES [J].
CHEN, KM ;
YEUNG, ES .
JOURNAL OF CHEMICAL PHYSICS, 1978, 69 (01) :43-52
[4]   THE SIGNIFICANCE OF FERMI RESONANCE FOR THE COLLISIONS OF TRIATOMIC-MOLECULES WITH ATOMS [J].
CLARY, DC .
CHEMICAL PHYSICS LETTERS, 1980, 74 (03) :454-458
[5]   Theoretical study of the CH4+F->CH3+FH reaction .1. Ab initio reaction path [J].
Corchado, JC ;
EspinosaGarcia, J .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (08) :3152-3159
[6]   Vibrational state control of bimolecular reactions: Discovering and directing the chemistry [J].
Crim, FF .
ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (10) :877-884
[7]   Reactive excitation functions for F plus p-H2/n-H2/D2 and the vibrational branching for F+HD [J].
Dong, F ;
Lee, SH ;
Liu, K .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (09) :3633-3640
[8]  
Herzberg G., 1966, MOL SPECTRA MOL STRU, V3
[9]   Vibrational control in the reaction of methane with atomic chlorine [J].
Kim, ZH ;
Bechtel, HA ;
Zare, RN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (50) :12714-12715
[10]   The exoergic F+CH4 reaction as an example of peripheral dynamics [J].
Kornweitz, H ;
Persky, A ;
Levine, RD .
CHEMICAL PHYSICS LETTERS, 1998, 289 (1-2) :125-131