Fine-structure state resolved rotationally inelastic collisions of CH(A 2Δ,v=0) with Ar:: A combined experimental and theoretical study

被引:26
作者
Kind, M [1 ]
Stuhl, F
Tzeng, YR
Alexander, MH
Dagdigian, PJ
机构
[1] Ruhr Univ Bochum, D-44780 Bochum, Germany
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[3] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
关键词
D O I
10.1063/1.1346642
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 collaborative experimental and theoretical study of rotationally inelastic collisions of CH(A (2)Delta,upsilon = 0) resolved rotational/fine-structure levels with argon is presented. Experimental state-to-state rate constants were extracted from CH A (2)Delta --> X (2)Pi fluorescence spectra upon laser excitation to individual levels in the A (2)Delta state in the presence of Ar. Fluorescence detection of the collision-induced population permits resolution of the fine-structure levels at low N, but no Lambda -doublet discrimination. For the lowest value of N (N = 2), the dominant process is the DeltaN = 0 fine-structure-changing transition, and the efficiency of this transition decreases markedly with increasing N. There is an increasing preference for conservation of the fine-structure label in DeltaN not equal 0 transitions as N increases. These rate constants have been compared to and interpreted with theoretical rate constants computed through quantum coupled-states calculations of cross sections based on ab initio CH(A (2)Delta)-Ar potential energy surfaces determined by Kaledin and Heaven (to be published). The tendency to conserve the fine-structure label is attributed to the Hund's case (b) nature of the CH(A (2)Delta) state, for which the electron spin is a spectator in the collision. (C) 2001 American Institute of Physics.
引用
收藏
页码:4479 / 4489
页数:11
相关论文
共 48 条
[11]   Rotational energy transfer in CD(A2Δ, ν=0) in collisions with Ar [J].
Cerezo, C ;
Torres, R ;
Ruiz, J ;
Martin, M .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2000, 132 (1-2) :19-24
[12]  
CHEN C, 1993, CHEM PHYS LETT, V203, P207
[13]   COLLISIONAL REMOVAL RATES FOR ELECTRONICALLY EXCITED CH RADICALS B2-SIGMA- AND C2-SIGMA+ [J].
COOPER, JL ;
WHITEHEAD, JC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1992, 88 (16) :2323-2327
[14]   ROTATIONAL AND VIBRATIONAL-ENERGY TRANSFER IN CH(A2-DELTA) [J].
COOPER, JL ;
WHITEHEAD, JC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1993, 89 (09) :1287-1290
[16]   THE INELASTIC-SCATTERING OF 2-PI-[CASE(B)] MOLECULES AND AN UNDERSTANDING OF THE DIFFERING LAMBDA-DOUBLET PROPENSITIES FOR MOLECULES OF PI VS PI-3 ORBITAL OCCUPANCY [J].
DAGDIGIAN, PJ ;
ALEXANDER, MH ;
LIU, K .
JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (02) :839-848
[17]   COLLISIONALLY INDUCED ROTATIONAL ENERGY-TRANSFER WITHIN THE ALPHA-2-DELTA STATE OF CH [J].
DIXON, RN ;
NEWTON, DP ;
RIELEY, H .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1987, 83 :675-682
[18]   The high-pressure range of the reaction of CH((2)Pi) with N-2 [J].
Fulle, D ;
Hippler, H .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (13) :5423-5430
[19]   COLLISIONAL QUENCHING AT 300-K - CH(A 2-DELTA) BY H2O, NH3 AND OTHER GASES AND NH(A 3-PI) BY H2O [J].
HEINRICH, P ;
KENNER, RD ;
STUHL, F .
CHEMICAL PHYSICS LETTERS, 1988, 147 (06) :575-580
[20]  
Herzberg G., 1950, Molecular spectra molecular structure: Spectra of diatomic molecules, V2nd ed.