Department of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520-8107, USA.
J Am Chem Soc. 2010 Jun 30;132(25):8766-73. doi: 10.1021/ja1023755.
The Thorpe-Ingold hypothesis for the gem-dimethyl effect in the cyclization reactions of 2-chloroethoxide derivatives has been investigated computationally in the gas phase and in aqueous solution. Ab initio MP2/6-311+G(d,p) and CBS-Q calculations reveal little intrinsic difference in reactivity with increasing alpha-methylation for the series of reactants 1-3. However, inclusion of continuum hydration or of explicit hydration through mixed quantum and statistical mechanics (MC/FEP) simulations does reproduce the substantial, experimentally observed rate increases with increasing alpha-methylation. Analysis of the MC/FEP results provides clear evidence that the rate increases stem primarily from increased steric hindrance to hydration of the nucleophilic oxygen atom with increasing alpha-methylation. Thus, the gem-dimethyl acceleration of oxirane formation for 1-3 is found to be predominantly a solvent effect.
气相和水溶液中 2-氯乙氧基衍生物环化反应的 Thorpe-Ingold 假说的 gem-二甲基效应已通过计算进行了研究。从头算 MP2/6-311+G(d,p) 和 CBS-Q 计算表明,对于反应物 1-3 系列,随着α-甲基化程度的增加,反应性的内在差异很小。然而,通过混合量子和统计力学(MC/FEP)模拟包含连续体水合作用或显式水合作用确实再现了随着α-甲基化程度的增加而观察到的实质性的、实验上的速率增加。对 MC/FEP 结果的分析提供了明确的证据,表明速率的增加主要归因于随着α-甲基化程度的增加,亲核氧原子的水合受到增加的空间位阻。因此,1-3 中环氧化合物形成的 gem-二甲基加速主要是溶剂效应。