Capture of asymmetric top dipolar molecules by ions: Rate constants for capture of H2O, HDO, and D2O by arbitrary ions

被引:20
|
作者
Maergoiz, A. I. [2 ]
Nikitin, E. E. [2 ,3 ]
Troe, J. [1 ,2 ]
机构
[1] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[3] Technion Israel Inst Technol, Schulich Fac Chem, IL-32000 Haifa, Israel
关键词
Ion-dipole capture; Asymmetric top; Data base for astrochemistry; Statistical adiabatic channel model; ADIABATIC CHANNEL MODEL; FAST CHEMICAL-REACTIONS; TRAJECTORY CALCULATIONS; LOW-TEMPERATURES; SYMMETRICAL-TOP;
D O I
10.1016/j.ijms.2008.08.019
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The capture of rotationally state-selected and unselected asymmetric top polar molecules by ions is investigated. Analytical expressions (for all rotational states up to j = 2) of capture rate constants in the perturbed-rotor second-order limit are derived for application to low temperature conditions. Approximate analytical representations over wider temperature ranges are also given for rotationally unselected molecules. The capture of H2O, D2O, and HDO by arbitrary ions is chosen for demonstration of the approach. Capture rate constants for the about 60 reactions of H2O with ions listed in the UMIST 2006 data base for astrochemistry are calculated, compared with experimental data, and represented in the format k(cap)(T) approximate to C-1 + C-2(T/300 K)(-1/2). The parameters C-1 and C-2 can be predicted in a very simple way. The approach allows one to identify capture-controlled mechanisms and/or to trace experimental artifacts. The approach applies equally well to the capture of symmetric top and linear dipole molecules by arbitrary ions. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 49
页数:8
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