Variable-Temperature Rate Coefficients of Proton-Transfer Equilibrium Reaction C2H4 + H3O+ ⇆ C2H5+ + H2O Measured with a Coaxial Molecular Beam Radio Frequency Ring Electrode Ion Trap

被引:2
|
作者
Smith, Mark A. [1 ,2 ,3 ]
Yuan, Bing [2 ]
Sanov, Andrei [2 ]
机构
[1] Univ Houston, Smith Coll Nat Sci & Math, Dept Chem, Houston, TX 77204 USA
[2] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
[3] Univ Arizona, Dept Planetary Sci, Lunar & Planetary Lab, Tucson, AZ 85721 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2012年 / 116卷 / 47期
基金
美国国家科学基金会;
关键词
ION-MOLECULE REACTION; GAS-PHASE BASICITIES; ALIPHATIC-HYDROCARBONS; AFFINITIES; DYNAMICS; ENERGY; SCALE; WATER; H2O;
D O I
10.1021/jp306372v
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 rate coefficients for the forward and reverse proton-transfer reactions C2H4 + H3O+ reversible arrow C2H5+ + H2O are studied with respect to independent varied neutral molecule and ion temperatures. The measurements are performed using a coaxial molecular beam radio frequency ring electrode ion trap at trap temperatures down to 23 K and beam temperatures up to 450 K. The temperature-dependent rate coefficients suggest that in this temperature window, the reaction proceeds through a statistically equilibrated complex. In order to explain the observed rate coefficients, a new type of reaction temperature was defined in these studies that considered collisional and internal (rotational and vibrational) degrees of freedom of both H3O+ and C2H4. The enthalpy and entropy of the equilibrium reaction deduced from a Van't Hoff plot are Delta H = (5.1 +/- 0.5) kJ.mol(-1) and Delta S = (-15.0 +/- 0.9) J.mol(-1).K-1, respectively.
引用
收藏
页码:11596 / 11600
页数:5
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