The Importance of NO+(H2O)4 in the Conversion of NO+(H2O)n to H3O+(H2O)n: I. Kinetics Measurements and Statistical Rate Modeling

被引:19
作者
Eyet, Nicole [1 ,2 ]
Shuman, Nicholas S. [1 ]
Viggiano, Albert A. [1 ]
Troe, Juergen [3 ,4 ]
Relph, Rachael A. [5 ]
Steele, Ryan P. [5 ]
Johnson, Mark A. [5 ]
机构
[1] USAF, Space Vehicles Directorate, Res Lab, Hanscom AFB, MA 01731 USA
[2] St Anselm Coll, Dept Chem, Manchester, NH 03102 USA
[3] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
[4] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[5] Yale Univ, Dept Chem, New Haven, CT 06520 USA
关键词
ADIABATIC CHANNEL MODEL; ION-MOLECULE CAPTURE; RATE CONSTANTS; CLUSTER IONS; WATER; TEMPERATURE; SPECTROSCOPY; DEPENDENCE; HYDRATION; MECHANISM;
D O I
10.1021/jp2032803
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 kinetics for conversion of NO+(H2O)(n) to H3O+(H2O)(n) has been investigated as a function of temperature from 150 to 400 K. In contrast to previous studies, which show that the conversion goes completely through a reaction of NO+(H2O)(3,) the present results show that NO+(H2O)(4) plays an increasing role in the conversion as the temperature is lowered. Rate constants are derived for the clustering of H2O to NO+(H2O)(1-3) and the reactions of NO+(H2O)(3,4) with H2O to form H3O+(H2O)(2,3), respectively. In addition, thermal dissociation of NO+(H2O)(4) to lose HNO2 was also found to be important. The rate constants for the clustering increase substantially with the lowering of the temperature. Flux calculations show that NO+(H2O)(4) accounts for over 99% of the conversion at 150 K and even 20% at 300 K, although it is too small to be detectable. The experimental data are complimented by modeling of the falloff curves for the clustering reactions. The modeling shows that, for many of the conditions, the data correspond to the falloff regime of third body association.
引用
收藏
页码:7582 / 7590
页数:9
相关论文
共 28 条
[1]   The critical hydration reactions of NO+ and NO2+ [J].
Angel, L ;
Stace, AJ .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (05) :1713-1715
[2]   Ab initio electron correlated studies on the intracluster reaction of NO+(H2O)n → H3O+(H2O)n-2 (HONO) (n=4 and 5) [J].
Asada, Toshio ;
Nagaoka, Masataka ;
Koseki, Shiro .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (04) :1590-1596
[3]   Infrared spectroscopy of size-selected water and methanol clusters [J].
Buck, U ;
Huisken, F .
CHEMICAL REVIEWS, 2000, 100 (11) :3863-3890
[4]  
Chase M.W., 1998, JANAF-Thermochemical Tables, VFourth
[5]   VIBRATIONAL SPECTROSCOPY OF NO+(H2O)(N) - EVIDENCE FOR THE INTRACLUSTER REACTION NO+(H2O)(N)-]H3O+(H2O)(N-2) (HONO) AT N-GREATER-THAN-OR-EQUAL-TO-4 [J].
CHOI, JH ;
KUWATA, KT ;
HAAS, BM ;
CAO, YB ;
JOHNSON, MS ;
OKUMURA, M .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (10) :7153-7165
[6]  
FEHSENFELD FC, 1971, J CHEM PHYS, V55, P2120, DOI 10.1063/1.1676383
[7]  
FEHSENFELD FC, 1969, J GEOPHYS RES, V74
[8]   KINETICS AND TEMPERATURE-DEPENDENCE OF HYDRATION OF NO+ IN GAS-PHASE [J].
FRENCH, MA ;
HILLS, LP ;
KEBARLE, P .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1973, 51 (03) :456-461
[9]   MECHANISM AND RATE CONSTANTS OF ION-MOLECULE RFACTIONS LEADING TO FORMATION OF H+(H2O)N IN MOIST OXYGEN AND AIR [J].
GOOD, A ;
DURDEN, DA ;
KEBARLE, P .
JOURNAL OF CHEMICAL PHYSICS, 1970, 52 (01) :222-&
[10]   Experimental and modeling study of the ion-molecule association reaction H3O++H2O(+M)→H5O2+(+M) -: art. no. 054303 [J].
Hamon, S ;
Speck, T ;
Mitchell, JBA ;
Rowe, B ;
Troe, J .
JOURNAL OF CHEMICAL PHYSICS, 2005, 123 (05)