On the origin of the steric effect

被引:68
作者
Pinter, Balazs [1 ]
Fievez, Tim [1 ]
Bickelhaupt, F. Matthias [2 ,3 ]
Geerlings, Paul [1 ]
De Proft, Frank [1 ]
机构
[1] Vrije Univ Brussel, Eenheid Algemene Chem ALGC, Brussels, Belgium
[2] Vrije Univ Amsterdam, Dept Theoret Chem, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Amsterdam Ctr Multiscale Modeling, Amsterdam, Netherlands
关键词
NUCLEOPHILIC-SUBSTITUTION; CONFORMATIONAL-ANALYSIS; DISPLACEMENT-REACTIONS; ALKYL-GROUPS; BASIS-SETS; HYDROLYSIS; POLAR; SOLVOLYSIS; CHEMISTRY; ENERGY;
D O I
10.1039/c2cp41090g
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
A quantitative analysis of the steric effect of aliphatic groups was carried out from first principles. An intuitive framework is proposed that allows the separation and straightforward interpretation of two contributors to the steric effect: steric strain and steric shielding (hindrance). When a sterically demanding group is introduced near a reactive center, deformation of its reactive zone will occur. By quantifying this deformation, a convincing correlation was established with Taft's steric parameters for groups of typical size, supporting the intuitive image of steric shielding; bulky groups slow down the reaction by limiting the accessibility of the reactive centre. On the other hand, the strong initial repulsion between the reactant and the substrate by means of the filled-filled orbital interaction results in the deformation of the substrate as well as a less stabilizing reaction zone, which are the manifestations of the steric strain. We thus conclude that both steric strain and steric hindrance can be derived from the Pauli repulsion evolving between the reactants in the course of the reaction.
引用
收藏
页码:9846 / 9854
页数:9
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