Reactions of H3O+(H2O)n and H+(H2O)n(CH3COCH3)m with CH3SCH3

被引:12
作者
Arnold, ST [1 ]
Thomas, JM [1 ]
Viggiano, AA [1 ]
机构
[1] USAF, Res Lab, Space Vehicles Directorate, Space Phys Models Branch,VSBP, Hanscom AFB, MA 01731 USA
关键词
ion molecule; rate constants; proton hydrates; dimethylsulfide; chemical ionization mass spectrometry;
D O I
10.1016/S1387-3806(98)14143-X
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
We have measured the rate constants and product branching fractions for the reactions of water clusters and mixed water/acetone clusters, H3O+(H2O)(n) and H+(H2O)(n)(CH3COCH3)(m), reacting with dimethylsulfide, CH3SCH3. The proton hydrates react rapidly. For n = 0-2, the reactions proceed at the collision rate within experimental error, while the reaction efficiency decreases slightly for n = 3 and further for n = 4 and n 5. The product distributions for the higher clusters are mainly switching one H2O for the CH3SCH3. The product distributions appear to be affected by thermal dissociation at higher temperatures. The reactions of H+(H2O)(n)(CH3COCH3)(m) with CH3SCH3 are also rapid and proceed by switching both a CH3COCH3 and a H2O out of the primary ion. The rate constant for H+(CH3COCH3)(2) is very slow, although the addition of two H2O ligands increases reaction by a factor of 13 and 21, respectively. The reactivity of H+(H2O)(CH3COCH3)(3) decreases to a value close to that of H+(CH3COCH3)(2). These results indicate that H3O+(H2O)(n) ions can be used as chemical ionization agents for CH3SCH3 detection in the atmosphere and that use of the mixed cluster ions, H+(H2O)(n) (CH3COCH3)(m), would be problematic. (C) 1998 Elsevier Science B.V.
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页码:243 / 251
页数:9
相关论文
共 19 条
[1]   COMPETITION BETWEEN ELECTRON DETACHMENT AND MONOMER EVAPORATION IN THE THERMAL-DESTRUCTION OF HYDRATED ELECTRON CLUSTERS [J].
ARNOLD, ST ;
MORRIS, RA ;
VIGGIANO, AA .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (21) :9242-9248
[2]   MULTICOMPONENT CLUSTER IONS .1. THE PROTON SOLVATED BY CH3CN/H2O [J].
DEAKYNE, CA ;
MEOTNER, M ;
CAMPBELL, CL ;
HUGHES, MG ;
MURPHY, SP .
JOURNAL OF CHEMICAL PHYSICS, 1986, 84 (09) :4958-4969
[3]  
DEAKYNE CA, 1994, J MOL STRUC-THEOCHEM, V307, P217
[4]  
HUNTER EP, 1997, NIST STANDARD REFERE
[5]  
Ikezoe Y., 1987, Gas Phase Ion-Molecule Reaction Rate Constants through 1986
[6]   THERMOCHEMICAL DATA ON GAS-PHASE ION-MOLECULE ASSOCIATION AND CLUSTERING REACTIONS [J].
KEESEE, RG ;
CASTLEMAN, AW .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1986, 15 (03) :1011-1071
[7]   CONTINUOUS DETERMINATION OF DIMETHYLSULFIDE AT PART-PER-TRILLION CONCENTRATIONS IN AIR BY ATMOSPHERIC-PRESSURE CHEMICAL IONIZATION MASS-SPECTROMETRY [J].
KELLY, TJ ;
KENNY, DV .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1991, 25 (10) :2155-2160
[8]   THE WATER DIMER - THEORY VERSUS EXPERIMENT [J].
NEWTON, MD ;
KESTNER, NR .
CHEMICAL PHYSICS LETTERS, 1983, 94 (02) :198-201
[9]   GAS-PHASE REACTIONS OF SULFIDES, MERCAPTANS, AND DIMETHYL METHYLPHOSPHONATE WITH IONIC SPECIES DERIVED FROM ARGON AND WATER [J].
PASSARELLA, R ;
SHUL, RJ ;
KEESEE, RG ;
CASTLEMAN, AW .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1987, 81 :227-233
[10]   Temperature dependence of the rate constants and branching ratios for the reactions of Cl-(D2O)(1-3) with CH3Br and thermal dissociation rates for Cl-(CH3Br) [J].
Seeley, JV ;
Morris, RA ;
Viggiano, AA ;
Wang, HB ;
Hase, WL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (03) :577-584