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
相关论文
共 50 条
  • [31] Photodesorption of H2O, HDO, and D2O ice and its impact on fractionation (Research Note)
    Arasa, Carina
    Koning, Jesper
    Kroes, Geert-Jan
    Walsh, Catherine
    van Dishoeck, Ewine F.
    ASTRONOMY & ASTROPHYSICS, 2015, 575
  • [32] SOLVENT ISOTOPE EFFECTS ON CHEMICAL SHIFTS OF COMPLEX FLUORO IONS IN H2O AND D2O SOLUTIONS
    RADLEY, K
    REEVES, LW
    JOURNAL OF CHEMICAL PHYSICS, 1971, 54 (10): : 4509 - &
  • [33] ON THE THERMAL RELAXATION OF CO2 MOLECULES IN PRESENCE OF H2O OR D2O MOLECULES
    HUBBARD, JC
    SETTE, D
    JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1953, 25 (04): : 827 - 827
  • [34] TRANSFER OF INDIVIDUAL IONS FROM H2O TO D2O - GIBBS ENERGY OF TRANSFER OF DIMETHYLMALEATE ION
    VESALA, A
    JALAVA, JP
    ACTA CHEMICA SCANDINAVICA SERIES A-PHYSICAL AND INORGANIC CHEMISTRY, 1977, 31 (07): : 585 - 590
  • [35] Structural features of solvation complexes of K+ and Br- ions in H2O and D2O
    Ivanov, EV
    Abrosimov, VK
    RUSSIAN JOURNAL OF INORGANIC CHEMISTRY, 2000, 45 (06) : 968 - 975
  • [36] Fragmentation of transient water anions following low-energy electron capture by H2O/D2O
    Fedor, J.
    Cicman, P.
    Coupier, B.
    Feil, S.
    Winkler, M.
    Gluch, K.
    Husarik, J.
    Jaksch, D.
    Farizon, B.
    Mason, N. J.
    Scheier, P.
    Maerk, T. D.
    JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2006, 39 (18) : 3935 - 3944
  • [37] ROTATIONAL STATE DEPENDENCE OF RATE CONSTANTS FOR THE REACTION OF IONS WITH ASYMMETRIC-TOP MOLECULES AT VERY LOW-TEMPERATURES - APPLICATION TO THE N+/H2O SYSTEM
    DUBERNET, ML
    MCCARROLL, R
    ZEITSCHRIFT FUR PHYSIK D-ATOMS MOLECULES AND CLUSTERS, 1990, 15 (04): : 333 - 340
  • [38] CENTRIFUGAL STRETCHING IN H2O AND D2O
    BENEDICT, WS
    PHYSICAL REVIEW, 1949, 75 (08): : 1317 - 1317
  • [39] RADIOLUMINESCENCE OF H2O AND D2O ICE
    STEEN, HB
    HOLTENG, JA
    JOURNAL OF CHEMICAL PHYSICS, 1975, 63 (06): : 2690 - 2697
  • [40] PK VALUES FOR D2O AND H2O
    不详
    JOURNAL OF CHEMICAL EDUCATION, 1967, 44 (11) : 635 - &