Communication: Experimental and theoretical investigations of the effects of the reactant bending excitations in the F+CHD3 reaction

被引:47
作者
Czako, Gabor [1 ,2 ]
Shuai, Quan [3 ,4 ]
Liu, Kopin [3 ]
Bowman, Joel M. [1 ,2 ]
机构
[1] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
[2] Emory Univ, Cherry L Emerson Ctr Sci Computat, Atlanta, GA 30322 USA
[3] Acad Sinica, IAMS, Taipei 10617, Taiwan
[4] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
关键词
PRODUCT PAIRS; METHANE; SCATTERING; CHLORINE; DYNAMICS; MODEL;
D O I
10.1063/1.3490795
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 effects of the reactant bending excitations in the F+CHD3 reaction are investigated by crossed molecular beam experiments and quasiclassical trajectory (QCT) calculations using a high-quality ab initio potential energy surface. The collision energy (E-c) dependence of the cross sections of the F+CHD3(nu(b)=0,1) reactions for the correlated product pairs HF(nu')+CD3(nu(2)= 0,1) and DF(nu')+CHD2(nu(4)=0,1) is obtained. Both experiment and theory show that the bending excitation activates the reaction at low E-c and begins to inactivate at higher E-c. The experimental F+CHD3(nu(b)=1) excitation functions display surprising peak features, especially for the HF(nu'=3)+CD3(nu(2)=0,1) channels, indicating reactive resonances (quantum effects), which cannot be captured by quasiclassical calculations. The reactant state-specific QCT calculations predict that the nu(5)(e) bending mode excitation is the most efficient to drive the reaction and the nu(6)(e) and v(5)(e) modes enhance the DF and HF channels, respectively. (C) 2010 American Institute of Physics. [doi:10.1063/1.3490795]
引用
收藏
页数:4
相关论文
共 30 条
[1]   Effects of bending excitation on the reaction of chlorine atoms with methane [J].
Bechtel, HA ;
Camden, JP ;
Brown, DJA ;
Martin, MR ;
Zare, RN ;
Vodopyanov, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (16) :2382-2385
[2]   BOND-SPECIFIC CHEMISTRY - OD-OH PRODUCT RATIOS FOR THE REACTIONS H+HOD(100) AND H+HOD(001) [J].
BRONIKOWSKI, MJ ;
SIMPSON, WR ;
GIRARD, B ;
ZARE, RN .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (11) :8647-8648
[3]   A five-dimensional quantum dynamics study of the F(2P)+CH4 reaction [J].
Chu, Tianshu ;
Han, Keli ;
Espinosa-Garcia, Joaquin .
JOURNAL OF CHEMICAL PHYSICS, 2009, 131 (24)
[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]   Quasiclassical trajectory calculations of correlated product distributions for the F+CHD3(v1=0,1) reactions using an ab initio potential energy surface [J].
Czako, Gabor ;
Bowman, Joel M. .
JOURNAL OF CHEMICAL PHYSICS, 2009, 131 (24)
[6]   CH Stretching Excitation Steers the F Atom to the CD Bond in the F + CHD3 Reaction [J].
Czako, Gabor ;
Bowman, Joel M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (48) :17534-17535
[7]   Accurate ab initio potential energy surface, dynamics, and thermochemistry of the F+CH4→HF+CH3 reaction [J].
Czako, Gabor ;
Shepler, Benjamin C. ;
Braams, Bastiaan J. ;
Bowman, Joel M. .
JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (08)
[8]   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
[10]  
Hase W. L., 1998, Encyclopedia of Computational Chemistry, P399