Gas phase reactions of nitromethyl carbanion with CHCl3 and CCl4: A theoretical investigation

被引:4
|
作者
Li, Tao Hong [1 ]
Wang, Chuan Ming [2 ]
Yu, Shi Wen [3 ]
Xie, Xiao Guang [4 ]
机构
[1] SW Forestry Univ, Key Lab Forest Resources Conservat & Use SW Mt Ch, Kunming 650224, Peoples R China
[2] Honghe Univ, Dept Biol, Menzi 661100, Peoples R China
[3] Qujing Normal Univ, Dept Chem, Qujing 650011, Peoples R China
[4] Yunnan Univ, Dept Chem, Kunming 650091, Peoples R China
关键词
Nitromethyl Carbanion; Chloromethanes; Mechanism; H/Cl Exchange; DENSITY-FUNCTIONAL THEORY; POTENTIAL-ENERGY SURFACES; SET MODEL CHEMISTRY; GAUSSIAN-BASIS SETS; ELECTRON-TRANSFER; MOLECULAR CALCULATIONS; S(N)2 REACTIONS; ANION; ATOMS; EXCHANGE;
D O I
10.1016/j.comptc.2011.01.011
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 ion/molecule reactions of CH2NO2- with CCl4 and CHCl3 in gas phase have been theoretically investigated using BH&HLYP, B3LYP and MP2 methods with 6-31+G* and 6-311+G** basis sets. The experimentally observed H/Cl exchange reaction between CH2NO2- and CCl4 was found to include two individual reactions, the chlorine cation transferring from CCl4 to CH2NO2-; via a chlorine-attack transition state and the proton transferring from CH2ClNO2 to CCl3-; via a proton-attack transition state. The calculated energies indicate that the H/Cl exchange is both kinetically and thermodynamically favorable. The H/Cl exchange reaction was found to be also possible for CHCl3, but a notable activation barrier represented by a bridge-like transition state and strong endothermicity for the chlorine cation-transfer step make this reaction impossible under low-energy condition. The classic S(N)2 reactions between CH2NO2- and the two chloromethanes were also calculated and notable energy barriers were identified for them. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:304 / 309
页数:6
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