Institute of Chemistry, The Hebrew University of Jerusalem, 91904, Jerusalem, Israel.
Chem Soc Rev. 2018 Jul 17;47(14):5125-5145. doi: 10.1039/c8cs00354h.
This is a tutorial on use of external-electric-fields (EEFs) as effectors of chemical change. The tutorial instructs readers how to conceptualize and design electric-field effects on bonds, structures, and reactions. Most effects can be comprehended as the field-induced stabilization of ionic structures. Thus, orienting the field along the "bond axis" will facilitate bond breaking. Similarly, orienting the field along the "reaction axis", the direction in which "electron pairs transform" from reactants- to products-like, will catalyse the reaction. Flipping the field's orientation along the reaction-axis will cause inhibition. Orienting the field off-reaction-axis will control stereo-selectivity and remove forbidden-orbital mixing. Two-directional fields may control both reactivity and selectivity. Increasing the field strength for concerted reactions (e.g., Diels-Alder's) will cause mechanistic-switchover to stepwise mechanisms with ionic intermediates. Examples of bond breaking and control of reactivity/selectivity and mechanisms are presented and analysed from the "ionic perspective". The tutorial projects the unity of EEF effects, "giving insight and numbers".
这是一篇关于将外电场(EEF)用作化学变化效应物的教程。本教程指导读者如何构思和设计电场对键、结构和反应的影响。大多数影响可以理解为电场诱导的离子结构稳定化。因此,沿着“键轴”方向取向电场将有助于键的断裂。类似地,沿着“反应轴”方向取向电场,即“电子对从反应物转变为产物的方向”,将催化反应。翻转反应轴上的场取向将导致抑制。沿着反应轴以外的方向取向电场将控制立体选择性并消除禁阻轨道混合。双向场可以控制反应性和选择性。对于协同反应(例如 Diels-Alder 反应)增加场强将导致机理从分步机理向离子中间体转变。从“离子角度”呈现并分析了键断裂和控制反应性/选择性以及机理的实例。本教程展示了 EEF 效应的统一性,“提供了洞察力和数值”。