Comparison of near-threshold reactivity of ground-state and spin-orbit excited chlorine atoms with methane

被引:36
作者
Kim, ZH [1 ]
Alexander, AJ [1 ]
Bechtel, HA [1 ]
Zare, RN [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1063/1.1378042
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
A 4:1 mixture of CH4 and BrCl diluted in He are coexpanded into a vacuum chamber and the reaction of methane with atomic chlorine is initiated by photolysis of BrCl. Near 420 nm, the resulting mixture of ground- and excited-state chlorine atoms have spatial anisotropies of beta (phot)=-0.7 for the Cl(P-2(3/2))+Br channel and beta (phot)=+1.8 for the Cl-*(P-2(1/2))+Br channel. The speed-dependent spatial anisotropy beta (rxn)(nu) of the CH3(nu =0) reaction product is detected by 2+1 resonance-enhanced multiphoton ionization. Our results indicate that the Cl*+CH4 reaction is unimportant in the near-threshold collision energy range of 0.13-0.16 eV, whereas the reaction with ground-state Cl atoms with CH4 excited with one quantum in the nu (2) (torsion) or nu (4) (bending) mode is dominant. (C) 2001 American Institute of Physics.
引用
收藏
页码:179 / 183
页数:5
相关论文
共 29 条
[1]   Evaluated kinetic and photochemical data for atmospheric chemistry, organic species: Supplement VII [J].
Atkinson, R ;
Baulch, DL ;
Cox, RA ;
Hampson, RF ;
Kerr, JA ;
Rossi, MJ ;
Troe, J .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1999, 28 (02) :191-393
[2]   NON-ADIABATIC PHOTODISSOCIATION DYNAMICS OF BRCL [J].
CAO, JY ;
LOOCK, HP ;
QIAN, CXW .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1994, 72 (03) :758-761
[3]   Ion imaging studies of the Cl(2PJ) and Br(2PJ) atomic products resulting from BrCl photodissociation in the wavelength range 235-540 nm [J].
Cooper, MJ ;
Jackson, PJ ;
Rogers, LJ ;
Orr-Ewing, AJ ;
Whitaker, BJ ;
Ashfold, MNR .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (11) :4367-4377
[4]   Potential energy surface, thermal, and state-selected rate coefficients, and kinetic isotope effects for Cl+CH4→HCl+CH3 [J].
Corchado, JC ;
Truhlar, DG ;
Espinosa-García, J .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (21) :9375-9389
[5]   AB-INITIO PREDICTION OF THE ACTIVATION-ENERGY FOR THE ABSTRACTION OF A HYDROGEN-ATOM FROM METHANE BY CHLORINE ATOM [J].
DOBBS, KD ;
DIXON, DA .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (48) :12584-12589
[6]   THERMAL AND VIBRATIONAL-STATE SELECTED RATES OF THE CH4+CL[--]HCL+CH3 REACTION [J].
DUNCAN, WT ;
TRUONG, TN .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (22) :9642-9652
[7]   INTERPOLATED VARIATIONAL TRANSITION-STATE THEORY - PRACTICAL METHODS FOR ESTIMATING VARIATIONAL TRANSITION-STATE PROPERTIES AND TUNNELING CONTRIBUTIONS TO CHEMICAL-REACTION RATES FROM ELECTRONIC-STRUCTURE CALCULATIONS [J].
GONZALEZLAFONT, A ;
TRUONG, TN ;
TRUHLAR, DG .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (12) :8875-8894
[8]   2 PHOTON RESONANCE ENHANCED MULTIPHOTON IONIZATION SPECTROSCOPY AND STATE ASSIGNMENTS OF THE METHYL RADICAL [J].
HUDGENS, JW ;
DIGIUSEPPE, TG ;
LIN, MC .
JOURNAL OF CHEMICAL PHYSICS, 1983, 79 (02) :571-582
[9]   Reaction dynamics of atomic chlorine with methane: Importance of methane bending and torsional excitation in controlling reactivity [J].
Kandel, SA ;
Zare, RN .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (22) :9719-9727
[10]   Exploring the spin-orbit reactivity in the simplest chlorine atom reaction [J].
Lee, SH ;
Liu, KP .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (14) :6253-6259